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African elephant in the jungle.
USAID supports efforts to combat wildlife crime in Uganda. Owing to its multidimensional nature, wildlife crime is a global issue and a transnational threat. Failure to effectively combat it not only has implications on national security but also alienates the nation from its rich wildlife heritage, and prevents local communities achieving better standards of living.
Photo credit: Karin Bridger/USAID
Crocodile at water edge.
USAID supports efforts to combat wildlife crime in Uganda. Owing to its multidimensional nature, wildlife crime is a global issue and a transnational threat. Failure to effectively combat it not only has implications on national security but also alienates the nation from its rich wildlife heritage, and prevents local communities achieving better standards of living.
Photo credit: A.J. Plumptre/WCS
Edward Samuel Jones, Assistant Professor, University of Copenhagen
Presentation: How robust are composite indicators? An almost certain stochastic simulation approach
A team from the Jordanian Gendarmerie meets with the Congolese FPU in action supporting African-led International Support Mission to the Central African Republic (MISCA) Police to evaluate their support in deploying UN peacekeepers to the Central African Republic (CAR) in Bangui on 20 June 2014.
Fighting broke out in CAR when the mainly Muslim Seleka alliance seized power in a coup in March 2013. UN agencies estimate that 2 million people, almost half of the population, are in need of assistance. The Security Council voted on 10 April 2014 to send 12,000 peacekeepers to help return order to CAR.
UN Photo/Catianne Tijerina
Elephants
USAID supports efforts to combat wildlife crime in Uganda. Owing to its multidimensional nature, wildlife crime is a global issue and a transnational threat. Failure to effectively combat it not only has implications on national security but also alienates the nation from its rich wildlife heritage, and prevents local communities achieving better standards of living.
Photo credit: Ashley Netherton/USAID
Tourists visiting one of the national parks.
USAID supports efforts to combat wildlife crime in Uganda. Owing to its multidimensional nature, wildlife crime is a global issue and a transnational threat. Failure to effectively combat it not only has implications on national security but also alienates the nation from its rich wildlife heritage, and prevents local communities achieving better standards of living.
Photo credit: Helen Mason/USAID
La directora de Prosperidad Social, Tatyana Orozco de la Cruz, hizo la entrega oficial del Centro para el Adulto Mayor en el municipio de Marinilla, Antioquia. Durante este evento, la titular de la Entidad explicó las 5 claves + 1 para el desarrollo de la estrategia y los objetivos de la Entidad para 2017, en materia de superación de la pobreza multidimensional en Antioquia.
"La pobreza tiene muchas caras y por eso es esencial combatirla en todas sus aristas. En Colombia somos pioneros en la implementación del Índice de Pobreza Multidimensional[1], que trabaja bajo cinco dimensiones claves para erradicar la pobreza. Esto nos permite identificar las necesidades específicas de cada región y focalizar el trabajo; de esta forma, en Antioquia, durante el 2017 desde Prosperidad Social pondremos especial énfasis en 5 claves + 1", aseguró Tatyana Orozco, Directora de Prosperidad Social.
En esta línea, la Directora describió las 5 claves + 1:
- Primera clave: Educación. Más de 700 mil niños y jóvenes antioqueños serán beneficiados por el programa Más Familias en Acción. Así mismo, más de 12 mil Jóvenes del departamento se beneficiarán durante 2017 del programa Jóvenes en Acción que tiene como objetivo incentivar la educación de la población joven, en condición de pobreza y vulnerabilidad.
- Segunda clave: Empleo. Se apoyarán a más de 19 mil personas a través de los programas de Inclusión Productiva, impulsando la consecución de ingresos por trabajo y potencializando medidas que fortalezcan la situación socioeconómica de las familias. La inversión en este frente será de 9 mil millones de pesos
- Tercera clave: Infraestructura. Se llevarán a cabo más de ocho mil mejoramientos de vivienda y se invertirán más de 88 mil millones de pesos en 59 proyectos de infraestructura en el Departamento.
- Cuarta clave: Salud. A través de Más Familias en Acción continuaremos incentivando y monitoreando la realización de controles médicos periódicos en los niños cuyas familias participan del programa. Así mismo, la Red UNIDOS encargada de hacer controles de nutrición pasará de atender 86 mil personas en el departamento a 106 mil.
- Quinta clave: Niñez y juventud. La mayoría de nuestros programas busca llegar a los niños, adolescentes y jóvenes del departamento, es decir, tienen un enfoque especial en este segmento poblacional. Esto se une a la estrategia de Atención Integral a la Primera Infancia "De Cero a Siempre".
+1. Los programas de Prosperidad Social se ejecutan bajo parámetros y acuerdos de transparencia.
Todo esto brinda continuidad al trabajo que Prosperidad Social ha venido realizando en Antioquia, donde tan sólo en 2016 se invirtieron más de 320 mil millones de pesos. Por su parte, La inversión de Prosperidad Social durante 2017 en Antioquia será de 352 mil millones de pesos.
De esta forma, la Entidad reforzará la gestión en 2017 a través de los aspectos básicos del Índice de Pobreza Multidimensional, con el que se han identificado las necesidades puntuales de los antioqueños.
Según lo afirmó Orozco, además de trabajar de acuerdo a las cinco dimensiones del Índice de Pobreza Multidimensional, la gran clave está en hacerlo con transparencia de forma que los ciudadanos puedan involucrarse y seguir todos los procesos y acciones de la Entidad planea. "Para Prosperidad Social siempre será una prioridad garantizar que la ejecución de nuestros recursos sean comunicados de manera abierta a nuestros grupos de interés, por esto compartimos hoy con ustedes nuestros planes para 2017", agregó.
En 2011, Colombia fue el primer país en implementar el Índice de Pobreza Multidimensional (IPM) y hoy es referente en la gestión de políticas públicas que buscan atacar la pobreza en sus diferentes aspectos. En los últimos dos años Prosperidad Social ha logrado sacar a 800 mil personas de la pobreza multidimensional, cumpliendo así en más del 50% la meta de 1,5 millones para el 2018.
[1] El Índice de Pobreza Multidimensional fue creado por el Oxford Poverty & Human Development Initiative (OPHI) como un indicador que busca medir la pobreza desde una metodología multidimensional, e identificar las múltiples carencias a nivel de los hogares y las personas en los ámbitos de la salud, la educación y la calidad de vida. En Colombia, está basado en la evaluación de cinco dimensiones claves: las condiciones educativas del hogar, las condiciones de la niñez y la juventud, la salud, el trabajo y el acceso a los servicios públicos domiciliarios y el estado de la vivienda.
From left to right:
Toomas Vaks, Director of Cyber Security of the Government of Estonia
Adam Blackwell, OAS Secretary for Multidimensional Security
Date: October 20, 2014
Place: Washington, DC.
Credit: Juan Manuel Herrera/OAS
From left to right:
Adam Blackwell, OAS Secretary for Multidimensional Security
José Miguel Insulza, OAS Secretary General
Manuel Mondragón y Kalb, National Security Commissioner of Mexico
Date: November 22, 2013
Place: Medellín, Colombia
Credit: Government of Mexico
The next generation CRIND capable of transforming the SK700-N pumps into a powerful multidimensional profit centre.Click to view original image.
A Moroccan peacekeeper serving with the UN Multidimensional Integrated Stabilization Mission in the Central African Republic (MINUSCA) in Bangui briefs contracted truck drivers transporting military equipment and traveling with soldiers to Bambari on 14 June 2014.
UN Photo/Catianne Tijerina
Commissioned to work with SALT Research collections, artist Refik Anadol employed machine learning algorithms to search and sort relations among 1,700,000 documents. Interactions of the multidimensional data found in the archives are, in turn, translated into an immersive media installation. Archive Dreaming, which is presented as part of The Uses of Art: Final Exhibition with the support of the Culture Programme of the European Union, is user-driven; however, when idle, the installation "dreams" of unexpected correlations among documents. The resulting high-dimensional data and interactions are translated into an architectural immersive space.
Shortly after receiving the commission, Anadol was a resident artist for Google's Artists and Machine Intelligence Program where he closely collaborated with Mike Tyka and explored cutting-edge developments in the field of machine intelligence in an environment that brings together artists and engineers. Developed during this residency, his intervention Archive Dreaming transforms the gallery space on floor -1 at SALT Galata into an all-encompassing environment that intertwines history with the contemporary, and challenges immutable concepts of the archive, while destabilizing archive-related questions with machine learning algorithms.
In this project, a temporary immersive architectural space is created as a canvas with light and data applied as materials. This radical effort to deconstruct the framework of an illusory space will transgress the normal boundaries of the viewing experience of a library and the conventional flat cinema projection screen, into a three dimensional kinetic and architectonic space of an archive visualized with machine learning algorithms. By training a neural network with images of 1,700,000 documents at SALT Research the main idea is to create an immersive installation with architectural intelligence to reframe memory, history and culture in museum perception for 21st century through the lens of machine intelligence.
SALT is grateful to Google's Artists and Machine Intelligence program, and Doğuş Technology, ŠKODA, Volkswagen Doğuş Finansman for supporting Archive Dreaming.
Location : SALT Gatala, Istanbul, Turkey
Exhibition Dates : April 20 - June 11
6 Meters Wide Circular Architectural Installation
4 Channel Video, 8 Channel Audio
Custom Software, Media Server, Table for UI Interaction
For more information:
refikanadol.com/works/archive-dreaming/
Here, you can see the cut, as well as the two panels of color. They will overlap to create a multidimensional red, and depending on the parting of the hair, more pink or red will be visible.
At the Cluny Museum, medieval culture showcases its ancestral knowledge. It took five centuries to discover that the thymus and the genitals are connected, as seen in this statue of the first man to experience desire, through a dream about a mythical serpent.....
Within the thymus, regulation of the cellular crosstalk directing T cell development depends on spatial interactions within specialized niches. To create a spatially defined map of tissue niches guiding human postnatal T cell development, we employed the multidimensional imaging platform co-detection by indexing (CODEX) as well as cellular indexing of transcriptomes and epitopes sequencing (CITE-seq) and assay for transposase accessible chromatin sequencing (ATAC-seq). We generated age-matched 4- to 5-month-old human postnatal thymus datasets for male and female donors, identifying significant sex differences in both T cell and thymus biology. We demonstrate a possible role for JAG ligands in directing thymic-like dendritic cell development, identify important functions of a population of extracellular matrix (ECM)− fibroblasts, and characterize the medullary niches surrounding Hassall’s corpuscles. Together, these data represent an age-matched spatial multiomic resource to investigate how sex-based differences in thymus regulation and T cell development arise, providing an essential resource to understand the mechanisms underlying immune function and dysfunction in males and females.
The thymus is the primary organ responsible for the generation and selection of mature, functional, and self-tolerant T cells.1 Effective T cell development is a critical component of our immune system’s ability to accurately and exclusively identify and kill foreign entities such as pathogens. During early postnatal T cell development—the period in life when T cell development is most active2—thymic seeding progenitors migrate to the thymus and mature into thymocytes. Thymic architecture is highly organized to provide spatially defined, stage-specific signaling cues to migrating thymocytes that guide development toward functional mature T cells.3,4,5,6
Recent single-cell sequencing resources demonstrating the diversity of human thymus tissue are incongruous with our current framework of thymus structure and organization,7,8,9,10,11,12,13,14,15,16,17,18,19 which describe a general migratory path thymocytes take through the cortex and medulla during conventional αβT cell development. Spatial transcriptomic sequencing of human thymus has demonstrated a deeper granularity of thymic niches and their evolution during fetal development to support different waves of non-conventional T cells.19,20 However, our understanding of how human postnatal thymus niches support conventional and non-conventional T cell development, T-lineage branching, and alternative lineage development remains limited.3,4,6 T cells generated at this stage of postnatal human development will become the foundation of our immune system, patrolling the body for decades.21 Thus, insights into early postnatal thymus niche biology are crucial to understand how our adaptive immune system is built and how perturbations in postnatal T cell development may emerge as immune dysfunction later in life.
To create a spatially defined map of tissue niches guiding human postnatal T and alternative lineage cell development, we employed multi-dimensional spatial proteomic imaging using co-detection by indexing (CODEX),22,23 single-cell transcriptomic-proteomic profiling using cellular indexing of transcriptomes and epitopes sequencing (CITE-seq),24 and single-cell assay for transposase accessible chromatin sequencing (ATAC-seq).25 Given the emerging recognition of sex differences in thymus gene expression and function,26,27,28,29,30,31 we collected and analyzed samples from male and female donors. Our analysis identifies significant sex differences during early postnatal development that affect T cell and thymus biology through common and cell type-specific mechanisms. Additionally, we highlight key cell types contributing to thymic involution that exhibit sex-based differences in thymic growth and early transition toward adipogenesis. These data suggest that kinetic differences in thymic involution are present between sexes and, importantly, that mechanisms driving thymic involution begin early in life. Altogether, these data represent a powerful age-matched spatial multiomic resource to investigate how sex-based differences in thymus biology and T cell development arise, and how they contribute to sex differences in diseases caused by immune dysfunction.
Results
Spatial multiomic profiling of human postnatal thymus identifies sex-based differences in T cells and thymus biology
We performed single-cell CITE-seq, ATAC-seq, and CODEX imaging on 4–33 months human postnatal thymuses, including 6 (3 female and 3 male) 4- to 5-month-old age-matched samples (Table S1). Each donor sample was processed simultaneously for CODEX imaging and sequencing (Figure 1A). We included a comprehensive 137 antibody panel (Data S1), allowing us to compare epigenomic, transcriptomic, and proteomic expression kinetics across developing thymocytes and enabling direct comparison of cells identified via phenotypic expression in CODEX with cells captured via CITE-seq. Prior to sequencing, we enriched CD45− non-hematopoietic cells and CD25+CD8− regulatory T (Treg) cells to ensure coverage of low-abundance cell types. After quality control and computational merging of individually sequenced patient datasets, we obtained a total of 74,334 cells with CITE-seq, including 19,434 non-T-lineage cells, and captured 25,717 nuclei with ATAC-seq. Importantly, cell proximity in CODEX tissue niches was used to screen predicted receptor-ligand interactions.
Figure 1 Spatial multiomic analysis identifies sex-biased characteristics of thymic niches
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CITE-seq cells were clustered based on transcriptional expression and annotated based on marker gene and surface protein expression (Figure S1A; Table S2).7,8 ATAC-seq clusters were computationally labeled using CITE-seq reference cluster labels, which identified 34 ATAC-seq cluster transfer labels for dataset integration (Figures 1B and S1B). We captured 54,900 thymocytes spanning development from early thymic progenitors (ETPs) to mature single positive (SP) T cells, immature innate cells, innate-like cells, and Tregs. We identified three Treg populations expressing canonical lineage markers, namely Treg progenitors (Pro-Tregs), thymic Tregs (tTregs), and recirculating/resident Tregs (rrTregs).32 We also identified antigen-presenting cells, including B cells, mast cells, monocytes, and six populations of dendritic cells (DCs).33 In addition to the activated DCs (aDCs), plasmacytoid DCs (pDCs), DC1, and DC2/3 populations described by Park et al.,7 we found proliferating populations of pDCs and DC1. We also captured 7,093 epithelial cells, including cortical epithelial cells (cTECs), medullary epithelial cells (mTECs), activated mTECs, and mimetic TECs.
Importantly, we captured 7,721 mesenchymal cells, which contribute to negative selection and thymic involution.9,19,34,35,36 Subclustering identifies important mesenchymal cell types, including two populations of endothelial cells (ECs) defined by differential expression of Notch ligands (ECs, ECs (Notch)). Additionally, we identified lymphatic ECs (LECs), pericytes, vascular smooth muscle cells (VSMCs), and five distinct fibroblast cell types, including DPP4+ capsular fibroblasts (DPP4+ capFibs), capsule fibroblasts (capFibs), medullary fibroblasts (mFibs), KRT+ fibroblasts (KRT+ Fibs), and proliferating fibroblasts (Fibs (P)).
We imaged each tissue sample with a custom 48 antibody CODEX panel to study the architecture and function of niches guiding thymocyte development, aiming to define the niche characteristics guiding T-lineage branch points. Stage-specific thymocyte phenotyping markers (CD62L, CCR7, CD1A, CD5, CD7, CD4, CD8, CD3, CD45RO, CD45RA, FOXP3, and SATB1) identified CD3+ double positive cells (DPs) undergoing T-lineage commitment toward CD4 or CD8 T cells. Phenotyping markers for non-T-lineage hematopoietic cells (CD19, CD11c, CD11b, and CD68), epithelial cells (EPCAM and KRT5/8), mural cells (MCAM and SMA), ECs (CD31), and fibroblasts (PDGFRA) identified the remaining major cell types defining thymic niche architecture. Finally, we included functional markers to define patterns of antigen presentation (CD86), human leukocyte antigen (HLA) class I and II expression (HLA-ABC and HLA-DR,DP,DQ), adhesion ligands (ICAM and VCAM), Notch ligands (DLL1, DLL4, JAG1, and JAG2), T cell activation (PD-1), self-tolerance (PD-L1), proliferation (Ki67), and enzymatic regulation (15-PDGH). In sum, our CODEX panel enabled investigation of spatially regulated mechanisms directing human T cell development.
Using neural-network-driven cell segmentation and Leiden-based clustering,23 we identified individual cells within thymic tissue for each sample (Figure S1C). We annotated cell types based on tissue location and phenotypic expression compared with CITE-seq clusters (Figure 1C), performed proximity-based neighborhood clustering to identify niches,23 and annotated niches based on location and cell type composition (Figure 1D; Figure S1D). This analysis quantified proximity-based cell-cell interactions (Figure S1E) and served as a platform to interrogate spatially defined thymic niche biology via integrated sequencing-imaging analysis.
Because of known sex differences in thymus and T cell gene expression,31 we compared our age-matched male and female samples separately. In line with prior reports of sex-biased gene expression on autosomes,37,38,39,40 only 2% of male differentially expressed genes (DEGs) were found on the Y chromosome and 0.3% of female DEGs were found on the X chromosome (Tables S3 and S4). Gene set enrichment analysis (GSEA) on male vs. female cells for each cell type identified pathways commonly upregulated in either sex (Figure 1E; Data S1). Pathways differentially regulated across hematopoietic, epithelial, and stromal cells represent cell-intrinsic sex-based differences. Female cells have higher gene expression of transcription, energy regulation, and antigen presentation. Male cells, by contrast, have increased gene expression of proinflammatory signaling, amino acid metabolism, and G protein-coupled receptors (GPCR) signaling. The top differentially expressed energy regulation and metabolism pathways were similarly sex-biased in human kidney,41 suggesting multiple organs show consistent sex-biased enrichment of pathways linked to metabolism and energy production. Our data align with sex-biased trends identified in human induced pluripotent stem cell (iPSC) lines42 and other human organs,43 indicating these pathways often differ between male and female cells across various cell types.
By contrast, some pathways showed cell type-specific sex-biased enrichment. Female T and hematopoietic cells showed enrichment of interferon signaling, and female fibroblast and perivascular cells were enriched in extracellular matrix (ECM)-centric pathways (Figure 1E). Our dataset also identified differential sex-specific pathway enrichment between cell types. Gene expression indicated higher cytokine signaling in T cells and hematopoietic cells in females and in epithelial and mesenchymal cells in males (Figure 1E). These data show significant gene expression differences in male and female thymic cells. To demonstrate sex differences at the proteomic level, we identified genes with a log fold change greater than 1 that contributed to increased chemokine signaling in male T cells. CXCR4, an important chemokine receptor in thymocyte migration and development, had increased expression in male progenitor T (pro-T) cells, which we confirmed via flow cytometry (3 male, 3 female; p = 0.03; Figure S1F). As higher levels of cytokine and interferon signaling have been previously shown to influence thymus and T cell biology,44,45 our data suggest male and female T cells develop in different signaling environments and may respond differently to cytokine stimuli.
Next, we quantified cell type abundance within male and female tissues, demonstrating differences in cortical and medullary cell distributions between sexes. When normalized to the total number of cells per lobe, female thymus lobes contained significantly more DPs (p = 0.011) and cTECs (p = 0.0023). In males, we found significantly more SPs (p = 4.2 × 10−4), CD3+ DPs (p = 9.9 × 10−4), activated mTECs (p = 0.0014), and VSMCs (p = 2.4 × 10−6) (Figure 1F). Given that thymus lobules with more DPs and cTECs would have a greater proportion of cells undergoing positive selection and lobules with more medullary cells would have more cells undergoing negative selection, these data suggest that sex differences in cell type abundance may influence the resources directed toward specific stages of thymocyte selection. Alternatively, these results may suggest that male and female thymuses are developmentally asynchronous, with males exhibiting faster growth and involution kinetics, resulting in decreased cortical-to-medullary ratios even in early neonatal stages. We focused further analyses on sequential developmental niches, including analysis of sex differences in cell types and niches at each stage.
JAG1 skews ETP development toward thymic DCs
We first analyzed the cortico-medullary junction (CMJ) where cells home to the thymus (Figure 2A). This region recruits and supports ETPs10 and is composed of ECs, VSMCs, and pericytes expressing the Notch ligand JAG1 (Figures 2B and 2C). CITE-seq demonstrated that the cell adhesion molecule used by ETPs to enter the thymus, CD62L, is quickly downregulated upon CMJ entrance through the vasculature (Figure S2A). However, recently immigrated CD62L+ double negative cells are frequently located in the subcapsular zone (Figure S2B), suggesting that ETPs enter the thymus and rapidly migrate to a subcapsular niche where DLL4, a more potent Notch ligand, is highly expressed on fibroblasts and subcapsular epithelial cells (Figures 2D and S2C). However, the concentrated presence of JAG1 at the entry point indicates that ETPs are first exposed to this Notch ligand.
Figure 2 Thymic progenitors entering via the corticomedullary junction are exposed to a gradient of Notch ligands, which influence lineage specification
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CellChat46 pathway analysis showed that JAG1-NOTCH1 interactions between endothelial and perivascular cells are enriched with ETPs (Figure 2E), while JAG1-NOTCH2 and JAG1-NOTCH3 interactions are enriched with DC1, DC1 (P), DC2/3, and aDCs (Figures 2E–2G). These data suggest that JAG1 could induce commitment toward other hematopoietic lineages, such as pDCs, conventional DCs (cDCs), or macrophages, which are known to develop within the thymus.10 As JAG ligands induce weaker Notch induction,47,48,49,50 we hypothesized that early contact with ETPs could maintain T-lineage potential while cells migrate toward DLL4 in the subcapsular niche.
We first analyzed the ability of the four thymic Notch ligands to induce T-lineage commitment or alternative lineage development from cord-blood-derived CD34+ hematopoietic stem and progenitor cells (HSPCs) in a defined, feeder-free culture system44 (Figure 2H). We included titrated concentrations of granulocyte-macrophage colony-stimulating factor (GM-CSF), which is produced by mast cells at the CMJ, to support DC development.51 We found that only DLL1 and DLL4 ligands induce T-lineage commitment, whereas JAG ligands or no ligand controls supported myeloid cell development and did not induce T-lineage commitment (Figure S2D). Specifically, JAG ligands with GM-CSF skewed CD68+ DC development toward CD14− DC1 cells, while no ligand controls skewed CD68+ DC development toward CD14+ DC2/3 cells (Figures 2I and S2E).
Next, to test our hypothesis that Notch signals via JAG1 ligands could act as a bridge toward later DLL4 interactions, we analyzed cells grown on JAG1 for 3, 5, or 7 days prior to DLL4 transfer (Figure 2J). We found that cells cultured on JAG ligands or no ligands for 3 days maintained reduced T-lineage commitment compared with DLL1 or DLL4 cells (pJAG1 = 0.033; pJAG2 = 0.017), whereas cells cultured on JAG ligands for longer than 3 days lost T-lineage potential (Figure 2K), indicating that JAG ligands could not support T-lineage potential.
We next analyzed the contribution of different Notch ligands to the development of male and female ETPs (Figures S2F and S2G). Our data suggest that JAG ligand interactions are more abundant and diverse in females, with JAG1-NOTCH1 interactions enriched in female ETPs and DLL4 interactions enriched in male ETPs.
Together, these data suggest that timely migration from the CMJ to DLL4 ligands at the subcapsular zone is critical for T-lineage commitment, and exposure to JAG ligands at the CMJ can guide alternative lineage development toward thymic-derived DCs. Our data further demonstrate previously unrecognized sex-biased regulation by Notch ligands.
Analysis of the subcapsular zone identifies sex-based differences in fibroblast regulation of DP development and thymus growth
From the CMJ, ETPs migrate to the subcapsular zone via a CCL25-CCR9 chemokine gradient established by cTECs and directed to pro-T, DP (P), and DP2 (Q), but not DP1 (Q) cells (Figure 3A; Figure S3A). The subcapsular niche consists of JAG1+ VCAM1+ DCs, cTECs, capsular fibroblasts, DPP4+ capsular fibroblasts, and proliferating fibroblasts, which secrete and maintain spatially regulated ECM ligands to support sequential thymocyte development (Figures 3B and 3C; Figure S3B and S3C).
Figure 3 Fibroblasts in the subcapsular zone contribute to regulation of thymus biology and T cell progenitor development
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GSEA showed that DPP4+ capsule fibroblasts were enriched in HSP90 chaperone cycle for steroid hormone receptors (padjusted = 0.0065; 18/52 pathway genes significantly upregulated) (Data S1), suggesting an enhanced response to steroid hormones and supporting their role in sex hormone-based thymic involution.9 By contrast, capFibs were enriched for genes related to cytokine (interleukin [IL]-33, padjusted = 1.50 × 10−6; IL-34, padjusted = 3.56 × 10−7) and chemokine signaling (CCL2, padjusted = 5.10 × 10−40; CXCL3, padjusted = 0.020; CXCL12, padjusted = 1.78 × 10−8; CXCL14, padjusted = 3.63 × 10−15), functions previously attributed to TECs. Furthermore, CellChat identified cortical fibroblasts as major contributors to insulin growth factor (IGF) signaling through predicted signaling to cTECs, which are found in close proximity in the cortex (Figure S3D), via IGF2-IGF1R and IGF1-IGF1R axes, and to ETPs and β-selection cells, which were found under the capsule (Figure S2B), via an IGF2-IGF2R axis (Figures 3D–3F).
We next explored the role of proliferating fibroblasts. GSEA comparisons between capFibs and Fibs (P) showed marked differences in signal transduction pathways. CapFibs resembled traditional fibroblasts, which upregulate tyrosine kinase, angiogenesis, and ECM regulation and deposition pathways, whereas Fib (P) upregulates WNT signaling and cell sensing pathways, including genes involved in transient receptor potential (TRP) channels in the stimuli sensing channels pathway and taste receptors (TASRs) (Figure 3G; Data S1). Interestingly, CODEX images identified ECM− PDGFRa+ fibroblasts lacking extra domain A fibronectin (EDA-FN) expression, indicating that Fibs (P) are not involved in fibrotic matrix deposition unlike capFibs (Figure 3H; Figure S3B). Fibs (P) form a network of PDGFRa+ cells throughout the cortex that does not overlap with the cTEC network, yet maintain cell-cell contact in specific niches and often localize near cortical capillaries (Figure S3D).
We found sex-specific differences in vascular endothelial growth factor A (VEGFA) signaling within ECM− fibroblasts (Fib (P)) and other mesenchymal cells. Although all thymic fibroblasts produce the angiogenesis growth factor VEGFA, male fibroblasts express more than female cells (Fibs (P): padjusted = 0.0306; DPP4+ capFibs: padjusted = 0.0318; mFibs: padjusted = 1.85 × 10−6) (Figure 3I). Given that postnatal male thymuses are larger than female thymuses in humans and primates26 (Figure S3E), male fibroblasts may provide increased VEGFA to support angiogenesis and rapid thymic growth observed during postnatal development.52 Additionally, male mFibs have higher expression of FGF7 (padjusted = 0.0154), which regulates thymus size.53 CellChat predicts that male Fibs (P) are enriched in FGF10 compared with females, which supports cTEC proliferation and vascular growth,53,54 and only male VSMCs express FGF18 (Figures S3F–S3H). These sex biases in fibroblast growth factor (FGF) gene expression may contribute to the larger size of early postnatal male thymuses by stimulating epithelial and EC growth and proliferation.
Comparison of DEGs between male and female mesenchymal cells found increased expression of adipogenesis, cytokine, and GPCR signaling pathways in DPP4+ capFibs (Figure 3J). We also found increased expression of APOD, a gene associated with androgen, estrogen, progesterone, and glucocorticoid signaling,55,56 across male fibroblast populations (Fibs (P): padjusted = 2.18 × 10−26, mFibs: padjusted = 8.45 × 10−32) (Figure S3I). Given the association of hormone signaling with thymic involution,29,52,57 these findings suggest early initiation of thymic involution in postnatal males.
In sum, we identified three roles for fibroblasts within the subcapsular niche: maintaining tissue structure and organization via ECM and chemokine signaling, directly regulating cTEC maintenance and expansion, and potentially coordinating T cell development directly through growth factors and cell-cell interactions.
Human postnatal thymocytes may self-select in the cortex to support positive selection of conventional αβT cells
Upon exiting the subcapsular zone, DPs migrate into the inner cortex toward the medulla, where they receive positive selection signals that guide T-lineage branching toward CD4 or CD8 SP cells (Figure 4A). For DPs to transition toward the CD4 lineage, cells must receive T cell receptor (TCR) stimulation through HLA class II interactions, yet previous mouse studies have shown transcriptional downregulation of HLA class I and II in DPs.58,59 Low transcriptional expression is hypothesized to prevent thymocyte-thymocyte self-selection during positive selection, necessitating DP interactions with cTECs to receive positive selection signals.
Figure 4 HLA class I and II interactions may support thymocyte positive selection in the inner cortical zone
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Analogous to mouse literature, quiescent human DPs do not express HLA class II transcripts and have closed CIITA promoters (Figures 4B and 4C). Despite the lack of class II mRNA, thymocytes express low levels of HLA class II protein throughout development (Figure 4B). Additionally, in contrast to mouse data, we observe constitutive class I mRNA expression, which increased as cells transitioned toward SPs (Figure 4D). This is consistent with ATAC-seq data demonstrating that the B2M promoter is open throughout thymocyte development (Figure 4E). We confirmed HLA expression via flow cytometry and found that approximately 25% of DPs express both class I and II, and over 65% of DPs are class I+ (Figure S4A). Thus, thymocyte self-selection within the cortex could support positive selection. In support of this notion, CODEX enabled us to identify locations within the cortex devoid of epithelial, fibroblast, endothelial, or DCs but packed with DPs expressing class II+ molecules concentrated at cell junctions (Figure 4F). We confirmed the absence of spindle-like cTEC projections in this niche via confocal imaging (Figure 4G). Additionally, we quantified cell-cell interactions and identified a niche (positive selection niche 1) consisting of class II+ DPs and CD3+ DPs and a niche (self-selection niche) containing mainly class II+ DPs (Figure 1D). Finally, we sorted thymocytes to isolate immature DPs (CD4+CD8+CD3−TCR−) and mature DPs (CD4+CD8+CD3+TCR+) from three donors and cultured them for 7 days in a feeder-free assay. In the absence of epithelial cells, both immature and mature DPs upregulate HLA class II proteins (Figure 4H), and immature DPs continue to mature along their developmental pathway, as indicated by increased percentage of CD27+ DPs in culture after 7 days (Figure 4I).
Next, we identified a niche that directs T-lineage commitment toward CD4 or CD8SPs. We performed differential gene expression analysis on clusters representing this lineage branch point to identify markers for our CODEX panel (Figure S4B). We found SATB1 expression increased as DPs transitioned toward SPs (Figure S4C), and compared with CD8SP transition cells, CD4SP transition cells had higher expression of this master transcription factor60 (Figures S4D and S4E). Imaging analysis confirmed increased SATB1 expression coincides with CD3 upregulation, consistent with a role in late DP development and lineage branching (Figure 4J).7 Neighborhood analysis identified a niche enriched for mature CD3+ DPs in the inner cortex, suggesting that there either exists a niche specifically for late DP development and CD4 lineage transition or that cells are pre-disposed to CD4 lineage development through their TCR and migrate as clonal populations after proliferation at the outer cortex.
We compared cortical niche organization between sexes and found differences in niche organization supporting conventional T cell development, self-selection, and cross presentation. Females showed increased neighborhood interactions between the cortical DC niche containing JAG1+ VCAM+ DCs and the mature DP niche containing CD3+ DPs, the positive selection niche 1 containing class II+ DP cells and CD3+ DP cells, and the positive selection niche 3 containing DCs and DPs (Figure S4F) as well as increased cell-cell interactions between cTECs and class II+ DPs (Figures S4G and S4H). Conversely, males had increased cell-cell interactions between cTECs and CD3+ DPs (Figures S4G and S4H). These data suggest that the proportionally larger female cortex could increase cross presentation from DCs and cTECs to class II+ DPs, possibly facilitating greater use of self-selection as an alternative mechanism for positive selection.
Taken together, spatial multiomic analysis of the inner cortex identified cortical niches supporting specific stages of DP development, including three positive selection niches, a specialized niche for self-selection, and a mature DP niche thymocytes migrate through prior to entering the medulla.
Spatial multiomics identifies key mechanisms regulating negative selection niches in the medulla
Mature DPs enter the medulla, an environment specialized for negative selection, and transition toward CD4 or CD8 lineages (Figure 5A). Within the medulla, cells specialized for negative selection localize around keratinized structures called Hassall’s corpuscles (HCs).61 HCs appear during late prenatal development and are abundant in human postnatal thymuses but rare in mice.62 Here, we demonstrate that HCs can be divided into three major components: an external epithelial border of highly keratinized cells, an inner border of cells expressing prostaglandin-degrading enzyme 15-PGDH (HPGD), and a central PDGFRa+ mass (Figure 5B). HCs produce thymic stromal lymphopoietin (TSLP),61 an analog of IL-7, which activates DCs to increase expression of class II and co-stimulatory molecules CD80 and CD86. Importantly, subclustering stromal populations identified a population of KRT+ fibroblasts resembling cells undergoing epithelial-to-mesenchymal transition (EMT)63 (Figures S5A and S5B). CITE-seq identified TSLP and 15-PGDH mRNA expression in KRT+ Fibs, mFibs, mTECs, activated mTECs, and aDCs (Figure 5C), implicating these cell types as potential contributors to the function of HCs. Finally, given the inner layer of 15-PGDH+ cells, we explored the role of prostaglandin signaling regulation within the medulla. We found that DC1 cells express high levels of PGE2, whereas DC2/3 cells and monocytes express the PTGER2 and PTGER4 receptors, and aDCs express the PTGER3 receptor (Figure 5C), suggesting prostaglandin signaling is a major regulator of DC activity near HCs.
Figure 5 HCs represent scalable organizing centers for negative selection in the neonatal thymic medulla
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CODEX imaging suggests HCs act as sub-medullary organizational centers to segregate the inner medulla into specialized niches for negative selection. CD86+ APCs, a subset of which express the co-stimulatory ligand CD40, localize near HCs and in direct contact with CD45RA+ mature SPs (Figure 5D; Figure S5C). In addition, approximately 30% of medullary area is composed of CD19+ B cells,64 which cluster into niches surrounding HCs (Figure S5D). These B cells are found in close contact with—and are often enveloped within—mTECs, potentially facilitating cross presentation with epithelial cells (Figure 5E). These results suggest thymic B cells may comprise an important source of antigen presentation for negative selection.64,65 We quantified medullary neighborhoods and identified six niches, including an mTEC maturation niche, a cross-presentation niche, and four niches specialized for negative selection, which vary in relative location to HCs or the CMJ, as well as their composition of APCs, epithelial, and T cells (Figure 1D; Figure S1D).
Negative selection niches surrounding HCs play a key role in conventional T cell and tTreg development.61 We enriched CD25+ cells for sequencing and found a population of CD25hi pro-Tregs expressing canonical Treg markers CTLA-4, TNFRSF1B (TNFR2), and TNFRSF4 (OX40); positive/negative selection markers (ITM2A, RANBP1, NCL, NME1, MIF, and ATP5G1); Treg developmental long non-coding RNA (MIR155HG)66,67,68,69; and other markers described in mice (Figure S5E). Whereas pro-Tregs expressed high levels of pro-apoptotic gene BCL2L11, mature tTreg subsets expressed the anti-apoptotic gene BCL2. Gene network reconstruction via SCENIC70 identified transcription factor networks activated during pro-Treg to tTreg transition (Figure 5F).
The thymus also contains mature, highly activated Tregs, labeled as rrTregs, believed to have recirculated from the periphery.71,72 rrTregs lack expression of CCR7 or thymic egress markers (KLF2 and S1PR1) but express IL1R2 (Figure S5F), which sequesters the inflammatory cytokine IL-1β to reduce local concentrations.73 CODEX imaging identified tTregs and rrTregs dispersed throughout the medulla, with rrTregs primarily adjacent to CD68+ DCs (Figure 5G). CellChat supported the potential of rrTregs to sequester inflammatory cytokines through interactions with DC2/3 via an IL-1β-IL-1R2 axis (Figure S5G). rrTregs also exhibited a tissue resident Treg phenotype (BATFhigh CCR8+) associated with wound healing and tissue regeneration function,74 and expressed remodeling and tissue repair-related genes such as matrix metalloproteinase enzymes (MMP25 and ADAM19) (Figure S5H). Overall, these findings illustrate Treg diversity in the thymus with their developmental trajectories and functions yet to be elucidated.
Comparisons of male and female rrTregs showed that male rrTregs had higher expression of IL-4 and IL-13, heat shock factor protein 1 (HSF1), and IL-1 signaling pathways (Figure 5H), suggesting rrTreg-mediated regulation of IL-1R2-mediated anti-inflammatory feedback checkpoints is a more prominent mechanism in male tTreg development in early postnatal thymus. Notably, male-activated mTECs have higher expression of CD40 and tumor necrosis factor (TNF) inflammatory pathways than females, possibly resulting in higher rrTreg activity (Figure S5I).
Finally, as Tregs have been shown in mouse to contribute to thymic involution through JAG1,75 we explored sex-based differences in tTreg gene expression. GSEA showed male rrTregs and tTregs have higher expression of adipogenesis pathways (Figures 5H and 5I). Given the presence of cells undergoing EMT, our data underlie the aggressive timeline of thymic involution and suggest that sex-based differences in thymus functional decline begin early in life.
Our detailed examination of the medulla identifies several niches specialized for negative selection, cross presentation, and mTEC maturation around HCs and demonstrates sex biases in inflammatory pathways and thymic involution kinetics within these niches.
Discussion
We performed spatial multiomics to construct a tissue atlas of niches guiding T cell development in early human postnatal thymus. These datasets characterize how key developmental niches drive lineage branch decisions, identify a possible mechanism for conventional αβT cell development through self-selection, and suggest additional functions for mesenchymal cell types governing thymus biology. Furthermore, we discovered several sex-specific differences in thymus cell and niche biology. As T cell development is a dynamic migratory process, knowledge of cell position in combination with proteomic, transcriptomic, and epigenomic sequencing data provides an invaluable resource to predict niche-specific signaling cues directing T cell development, and mechanisms responsible for maintaining tissue structure and directing thymic involution.
We describe an approach to sequencing analysis using multidimensional imaging to establish benchmarks for the location, ligand expression, and composition of key niches in T cell development. This enables us to analyze cell-cell interactions guided by niche composition, identifying physiologically relevant ligand-receptor interactions based on cell proximity within the tissue. Ultimately, this approach maps epigenomic, transcriptomic, and proteomic data to distinct tissue niches at single-cell resolution. Furthermore, we included equal numbers of male and female age-matched thymus samples, enabling comparison between sexes across platform modalities. Our analysis of sex-matched human early postnatal thymus demonstrates the highly plastic nature of thymus lobule organization and resource dedication. Each niche responds to sex-biased developmental kinetics, supporting robust T cell development to ultimately produce functional immune systems in different manners (Figure 6). The findings herein describe only a subset of the data, and we encourage the community to capitalize on this resource to provide further insight into sex differences and targeted niche-specific inquiries.
Figure 6 The human early postnatal thymus lobule is spatially organized into sex-biased niches to support stage-specific T cell development
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In our analysis of Notch ligands, we complemented our in silico approach with in vitro analysis. Our analysis suggests that JAG1 at the CMJ cannot support T-lineage commitment as cells migrate toward the subcapsular zone but instead skew alternative lineage development toward a CD14− DC1 subset (Figure 6). CD14 expression on DCs is linked with increased inflammatory cytokine production,76 suggesting that JAG ligands promote non-inflammatory DC phenotypes. These results highlight the importance of precise Notch signaling strength and timing in the thymus and emphasize the need for strict spatial control of different Notch ligands within thymic niches. Our observation of high JAG1 expression in the medulla and decreased DLL4 expression on cTECs outside the subcapsular zone aligns with previous studies on human postnatal thymus.77
In the subcapsular zone, we characterize the important roles of specialized fibroblasts. DPP4+ capFibs, described in mouse as cells with progenitor and anti-fibrotic potential,78,79,80,81,82 are observed as a fibroblast subset responsive to changes in systemic hormone levels. Since thymic function and involution are regulated by sex hormone levels,57,83,84,85 DPP4+ capFibs likely control these processes and are potential targets for addressing age-related thymic involution.86 Previously, only medullary fibroblasts were linked to thymocyte development and selection in the medulla.82 We demonstrate that capFibs may directly support thymocyte development in the cortex by producing growth factors like IGF2 (Figure 6). Blocking IGF2 signaling arrests thymocytes at the double negative stage,87 and our data identify capFibs as the IGF2 source, suggesting capFibs as an additional cell source of cytokines and growth factors for in vitro developmental systems. Finally, we demonstrate that ECM profiles of thymic fibroblasts are tightly regulated based on spatial localization. Future work should characterize how tissue stiffness changes as thymocytes migrate through developmental thymic niches to improve biomaterial strategies for in vitro T cell development.88
Furthermore, we identify a population of ECM− cortical fibroblasts that are enriched in cell sensing pathways, such as TASRs and TRP channels. Interestingly, TASRs regulate cell responses to local soluble substances, such as glucose, modulating release of hormones and other signaling molecules.89 Similarly, TRP channels play roles in cell sensing, such as pheromone signaling, nociception, temperature sensation, and osmoregulation.90 Given the proximity of these cells to vasculature in the cortex, Fibs (P) may play a critical role as regulatory cells by sensing environmental changes and modulating thymus size (Figure 6). Their lack of ECM production and network-like structure resemble fibroblast reticular cells (FRCs) in the lymph node, which rapidly proliferate and remodel the cortex during infection.91 Our data are generated from early postnatal thymus samples, an age with active T cell development, suggesting these fibroblasts expand the thymic cortex similarly to FRCs during infection, signaling through FGF and IGF to stromal and epithelial cells to orchestrate remodeling.
While the dogma in thymocyte positive selection suggests that DPs downregulate class II RNA to prevent self-selection and force interactions with cTECs,58,59 several studies suggest that T-lineage cells can select off each other to support CD4 T cell development.20,92,93,94 Here, we describe an inner cortical niche where class II+ DPs reside that may support positive selection via DP-DP self-selection (Figure 6). We show that immature DPs cultured without epithelial cells upregulate HLA class II and continue to mature and receive positive selection signals. Additionally, upregulated SATB1 expression identifies mature DPs in an inner cortical niche and the CD4 branch of their progeny, suggesting it may determine early lineage specificity. Future work should investigate critical features of this niche and SATB1’s role in thymocyte development.
Within the medulla, we identified a niche adjacent to HCs specialized for negative selection and highlighted the role of rrTregs in modulating the medullary inflammatory environment (Figure 6). The abundance of HCs in human but not mouse, and their proximity to negative selection niches, suggests these structures evolved to provide niche-level organization within the larger human medulla or to regulate negative selection more stringently in longer-lived species.
Comparing male and female tissue showed sex differences in both T cell and thymus biology. Studies on post-pubertal males and females show that sex hormones differentially regulate thymic involution between sexes,26,27,28,29,30,52,57,84,86 and that androgen blockers increase FOXN1 expression, thymic involution, and increased rejuvenation.29,30,52,84,86 Additionally, older males produce fewer recent thymic emigrants and have smaller thymuses compared with females.26,28 Some studies describe decreased numbers of AIRE+ mTECs with age and in females,95 potentially predisposing females who maintain greater thymic function later in life to autoimmune disease.29 These studies also observe less interlobular fat in young female thymus,26 suggesting differences in thymic involution kinetics begin pre-puberty. However, current literature has not addressed transcript-level sex differences underlying functional differences in thymic and immune function. Our analysis uncovers that female thymic cells upregulate energy regulation, transcription, and antigen-presentation pathways, whereas male cells increase proinflammatory signaling, amino acid metabolism, and GPCR signaling. These cell metabolic differences align with transcript-level sex differences in other organs41,42,43 and highlight the need for sex-based cell culture optimization in in vitro T cell culture systems.
In addition to changes common to other organs,40,41 we identify thymus-specific differences affecting key processes in thymocyte development and training. Females have a larger proportion of cortical cells per lobule, aligning with lower thymic involution rates and a larger cortex/medulla ratio.26,27,52 ETPs have enriched interactions with JAG1 as they migrate away from the CMJ, suggesting increased JAG1 interactions could skew ETP lineage commitment toward less inflammatory DC phenotypes (Figure 6). In the female cortex, we observe increased cTEC and class II+ DP interactions and increased interactions between cortical DC and positive selection niches, suggesting thymocyte self-selection may play a larger role during positive selection (Figure 6). Conversely, the female medulla shows decreased inflammatory pathway activation and fewer medullary cells. These data suggest females prioritize generating a larger repertoire of DPs over deleting autoreactive cells through negative selection, potentially contributing to sex differences in autoimmune disease prevalence in females.96
In males, we observe enriched DLL4 interactions with ETPs, which aligns with previous data demonstrating that androgen levels positively correlate with DLL4 on cTECs.29 The male cortex shows increased interactions with mature CD3+ DPs and cTECs, suggesting male thymocytes may have lower proliferation rates post β-selection, allowing sufficient space for positive selection. In the medulla, male-activated mTECs exhibit increased inflammatory pathway markers, and male Tregs exhibit higher inflammatory modulation and activate thymic involution pathways.75 Upregulation of inflammatory modulation by male rrTregs may regulate the higher proinflammatory signaling in male cells (Figure 6). Interestingly, post-pubertal males have more Tregs and fewer CD4 T cells than females, possibly due to a more inflammatory medullary environment skewing CD4 development toward the Treg lineage.31
We further explore sex differences in thymus size control mechanisms. Among fibroblast populations, we find significant differences in expression of growth and angiogenesis factors, such as VEGFA and FGFs, potentially contributing to the size difference in male and female thymuses at this age (Figure 6). These data align with and extend known sex differences in growth factor expression, including sex-biased expression of growth hormone and IGF-1 in regulating size of different tissues.97,98 Importantly, these results indicate sex-specific differences in early thymus structure maintenance and growth, which could skew T cell development. We also establish an early transition toward an adipogenic environment in males. These observations align with findings in model organisms, where young male rats exhibit higher rates of thymic involution52 and early postnatal male primates have a larger interlobular fat area.26 Together, these factors define two possible mechanisms contributing to a male-female difference in thymus size and involution kinetics.
Future studies should test how sex differences at the transcript, niche, and organ level impact differential T cell production and quality as well as explore how sex differences in other organs contribute to known differences in immune responses. Defined in vitro and organoid culture systems replicating the thymic microenvironment present powerful platforms to test if the cell type-specific and sex-specific differences identified here lead to increased autoimmune disease incidence among females and increased infection susceptibility in males. Furthermore, given the surprising sex-based differences at this early postnatal stage, future work should examine aged thymus to investigate how cellular level differences in thymic involution kinetics may translate to larger impacts on our immune system later in life.
Limitations of the study
Our analysis of intra-sex variation is limited by access to patient samples as well as the inability to conduct mechanistic experiments in the context of a whole organism. There is an opportunity for future work to further validate and expand on predicted ligand-receptor interactions.
The thymic epithelium is responsible for the secretion of thymic peptides, which intervene in some steps of intra- and extrathymic T cell differentiation. Recent data suggest that thymic hormone secretion is modulated by the neuroendocrine network, comprising thyroid, adrenals, and gonads. However, the role of the pituitary gland in this regulation is still poorly understood. In the present paper we studied the in vivo and in vitro influences of PRL on the secretion of thymulin, one of the chemically defined thymic hormones, by thymic epithelial cells (TEC). When injected daily (20-100 micrograms/20 g) in young or old C57BL/6 mice, PRL induced a specific increase in thymulin synthesis and secretion, respectively, measured by the number of thymulin-producing cells in the thymus and the peripheral levels of the hormone. This stimulation was dose dependent and reversible after the end of treatment. Similar findings have been made in animals with pituitary dwarfism, known to have low levels of circulating thymulin. This stimulatory effect was also observed in primary cultures of human and mouse TEC when PRL (10(-7) to 10(-8) M) was applied to culture supernatants, thus suggesting that PRL could act directly on TEC. In addition, we induced in vivo experimental hypoprolactinemia, treating mice with bromocriptine, a dopamine receptor agonist that inhibits pituitary PRL secretion. Bromocriptine treatment (100-200 micrograms/20 g) yielded a significant decrease in thymulin secretion that could be reversed by coincident treatment with PRL. In the light of previous observations that bovine GH can also increase thymulin production in aged dogs, we performed a series of experiments in vitro to evaluate whether GH has a direct effect on TEC. We observed that only human GH preparations that are known to have a PRL-like effect were efficient in stimulating thymulin biosynthesis and release into the culture supernatants. The effects of PRL on TEC were not restricted to thymic hormone production. We observed that TEC proliferation, as well as the numbers of a TEC subset defined by the expression of cytokeratins 3 and 10, could also be increased by PRL treatment. All these findings show that the pituitary gland directly affects TEC in terms of cytoskeletal and secretory protein expression as well as cell cycle.. This paper reviews the mechanism of sex hormone actions on the thymus, presenting mainly our data obtained at the cellular and molecular levels. First, data supporting the "genomic" action via the nuclear sex hormone receptor complexes are as follows: 1) sex hormone receptors and the thymic factor (thymulin) are co-localized in thymic epithelial cells, but not in T cells; 2) production/expression of thymic factors (thymulin, thymosin alpha 1) are remarkably inhibited by sex hormone treatment; 3) sex hormones cause changes in T cell subpopulations in the thymus; and 4) sex hormones strongly influence the development of thymus tumors in spontaneous thymoma BUF/Mna rats through their receptor within the tumor cells. Secondly, data indicating the "non-genomic" action of sex hormones via a membrane signal-generating mechanism are as follows: 1) the proliferation/maturation of thymic epithelial cells is mediated through protein kinase C activity introduced by sex hormones; 2) sex hormones directly influence DNA synthesis and cdc2 kinase (cell cycle-promoting factor) activity..
pubmed.ncbi.nlm.nih.gov/2737149/
www.cell.com/developmental-cell/fulltext/S1534-5807(24)00539-2
A Moroccan peacekeeper serving with the UN Multidimensional Integrated Stabilization Mission in the Central African Republic (MINUSCA) in Bangui briefs contracted truck driver transporting military equipment and traveling with soldiers to Bambari on 14 June 2014.
UN Photo/Catianne Tijerina
United Nations Police (UNPOL) Officers from Benin serving with the United Nations Multidimensional Integrated Stabilization Mission in Mali (MINUSMA) and Malian National Guard Officer conduct daily joint patrols in the streets of Gao, to ensure general security, maintain order and offer protection of civilians. They are escorted by Formed Police Unit (FPU) from the Burkina Faso Contingent. Photo MINUSMA/Marco Dormino
From left to right:
Farah Diva Urrutia, Secretary for Multidimensional Security
Luis Almagro, OAS Secretary General
Date: July 19, 2018
Place: Washington DC
Credit: Juan Manuel Herrera/OAS
Commissioned to work with SALT Research collections, artist Refik Anadol employed machine learning algorithms to search and sort relations among 1,700,000 documents. Interactions of the multidimensional data found in the archives are, in turn, translated into an immersive media installation. Archive Dreaming, which is presented as part of The Uses of Art: Final Exhibition with the support of the Culture Programme of the European Union, is user-driven; however, when idle, the installation "dreams" of unexpected correlations among documents. The resulting high-dimensional data and interactions are translated into an architectural immersive space.
Shortly after receiving the commission, Anadol was a resident artist for Google's Artists and Machine Intelligence Program where he closely collaborated with Mike Tyka and explored cutting-edge developments in the field of machine intelligence in an environment that brings together artists and engineers. Developed during this residency, his intervention Archive Dreaming transforms the gallery space on floor -1 at SALT Galata into an all-encompassing environment that intertwines history with the contemporary, and challenges immutable concepts of the archive, while destabilizing archive-related questions with machine learning algorithms.
In this project, a temporary immersive architectural space is created as a canvas with light and data applied as materials. This radical effort to deconstruct the framework of an illusory space will transgress the normal boundaries of the viewing experience of a library and the conventional flat cinema projection screen, into a three dimensional kinetic and architectonic space of an archive visualized with machine learning algorithms. By training a neural network with images of 1,700,000 documents at SALT Research the main idea is to create an immersive installation with architectural intelligence to reframe memory, history and culture in museum perception for 21st century through the lens of machine intelligence.
SALT is grateful to Google's Artists and Machine Intelligence program, and Doğuş Technology, ŠKODA, Volkswagen Doğuş Finansman for supporting Archive Dreaming.
Location : SALT Gatala, Istanbul, Turkey
Exhibition Dates : April 20 - June 11
6 Meters Wide Circular Architectural Installation
4 Channel Video, 8 Channel Audio
Custom Software, Media Server, Table for UI Interaction
For more information:
refikanadol.com/works/archive-dreaming/
Koen Davidse (centre right), Deputy Special Representative and Mbaranga Gasarabwe (centre right), Deputy Special Representative of the Secretary-General in the UN Multidimensional Integrated Stabilization Mission in Mali (MINUSMA) attend a town hall meeting with MINUSMA staff members at the MINUSMA Operational Base in Bamako.
Craig Anthony Miller
Thanks to brownstoner.com and curbed.com for featuring this photo:
www.brownstoner.com/brownstoner/archives/2011/03/tuesday_...
Thanks to Curbed for featuring this photo:
ny.curbed.com/archives/2011/03/29/caseshiller_falls_glass...
Beautiful jungle by Karuma Falls along the River Nile.
USAID supports efforts to combat wildlife crime in Uganda. Owing to its multidimensional nature, wildlife crime is a global issue and a transnational threat. Failure to effectively combat it not only has implications on national security but also alienates the nation from its rich wildlife heritage, and prevents local communities achieving better standards of living.
Photo credit: Karin Bridger/USAID
Commissioned to work with SALT Research collections, artist Refik Anadol employed machine learning algorithms to search and sort relations among 1,700,000 documents. Interactions of the multidimensional data found in the archives are, in turn, translated into an immersive media installation. Archive Dreaming, which is presented as part of The Uses of Art: Final Exhibition with the support of the Culture Programme of the European Union, is user-driven; however, when idle, the installation "dreams" of unexpected correlations among documents. The resulting high-dimensional data and interactions are translated into an architectural immersive space.
Shortly after receiving the commission, Anadol was a resident artist for Google's Artists and Machine Intelligence Program where he closely collaborated with Mike Tyka and explored cutting-edge developments in the field of machine intelligence in an environment that brings together artists and engineers. Developed during this residency, his intervention Archive Dreaming transforms the gallery space on floor -1 at SALT Galata into an all-encompassing environment that intertwines history with the contemporary, and challenges immutable concepts of the archive, while destabilizing archive-related questions with machine learning algorithms.
In this project, a temporary immersive architectural space is created as a canvas with light and data applied as materials. This radical effort to deconstruct the framework of an illusory space will transgress the normal boundaries of the viewing experience of a library and the conventional flat cinema projection screen, into a three dimensional kinetic and architectonic space of an archive visualized with machine learning algorithms. By training a neural network with images of 1,700,000 documents at SALT Research the main idea is to create an immersive installation with architectural intelligence to reframe memory, history and culture in museum perception for 21st century through the lens of machine intelligence.
SALT is grateful to Google's Artists and Machine Intelligence program, and Doğuş Technology, ŠKODA, Volkswagen Doğuş Finansman for supporting Archive Dreaming.
Location : SALT Gatala, Istanbul, Turkey
Exhibition Dates : April 20 - June 11
6 Meters Wide Circular Architectural Installation
4 Channel Video, 8 Channel Audio
Custom Software, Media Server, Table for UI Interaction
For more information:
refikanadol.com/works/archive-dreaming/
Durante la rendición de cuentas del Sector de la Inclusión Social y la Reconciliación, Tatyana Orozco directora de Prosperidad Social, anunció que las entidades que hacen parte de este sector, en 2016 invertirán en el Departamento de Chocó $181 mil millones.
Orozco afirmó que la continuidad en la reducción en las cifras de pobreza así como en la reparación a las víctimas del conflicto armado, la atención a la primera infancia y el permanente registro de los signos que ha dejado la violencia en Colombia, son los principales logros del Sector durante 2015.
Prosperidad Social, cabeza del sector, ejecutó programas y proyectos orientados a su objetivo mayor de la superación de la pobreza, trabajo gracias al cual 171.000 colombianos salieron de esta condición, mientras que 700.000 superaron la pobreza multidimensional.
2.559.954 hogares fueron beneficiados con los incentivos de salud y educación entregados por el programa Más Familias en Acción; mientras que 250.945 jóvenes se matricularon en "Jóvenes en Acción", de los cuales 94.246 culminaron sus estudios.
Las intervenciones de Prosperidad Social no sólo han llegado a los individuos y a las familias sino también a las comunidades. Se adelantaron 342 proyectos de infraestructura social con una inversión de $638 mil millones representados en vías urbanas y rurales, salones comunitarios y polideportivos.
Con el propósito de impulsar la generación de ingresos de la población, Prosperidad Social capacitó a las personas, en alianzas con el sector privado, para el desarrollo de diversas labores conducentes a su inserción en el mercado laboral, además de apoyar con capital semilla más de 7 mil emprendimientos colectivos en todo el país.
En 190 municipios colombianos, 86.724 familias consumen lo que siembran en sus patios gracias a la Red de Seguridad Alimentaria (ReSA). Por otra parte, 3.780 familias de 123 comunidades indígenas de la Alta Guajira cuentan con atención especial por parte de ReSA.
La Agencia Nacional para la Superación de la Pobreza Extrema (ANSPE), convertida ahora en Subdirección General para la Superación de la Pobreza de Prosperidad Social, acompañó con los cogestores de la Red Unidos a 1.007.532 familias, ayudando a 105.000 personas a superar la pobreza extrema. Entre 2011 y 2015, más de 360.000 hogares superaron esta condición. Así mismo ANSPE hizo un pilotaje de acompañamiento étnico a cinco territorios indígenas, lo que permitió que en 2016 se haya ampliado el número de territorios acompañados.
ANSPE estuvo acompañando a 194 mil hogares en su postulación a las 100.000 viviendas gratuitas del Gobierno Nacional. Con los beneficiarios de este programa trabajo en la construcción de planes comunitarios teniendo 19 ya consolidados.
Gracias a la gestión de oferta institucional de ANSPE, más de 4 millones de personas cuentan con documento de identificación; cerca de 1.5 millones de niños, niñas y jóvenes entre 5 y 17 años están estudiando; más de 4 millones de personas están afiliadas al régimen subsidiado de salud y 852.000 menores de 10 años están en programas de crecimiento y desarrollo.
ICBF
Cerca de 2 millones de niños y niñas menores de 5 años fueron atendidos durante el 2015 a través de las diferentes estrategias dirigidas a la Primera Infancia que lidera el Instituto Colombiano de Bienestar Familiar, 120 mil fueron beneficiarios de programas de Protección y 490 mil con acciones de apoyo nutricional.
Dentro los principales logros estratégicos del ICBF se destacó que gracias a la estrategia del Gobierno Nacional 'De Cero a Siempre', 1.1 millones de niños y niñas menores de 5 años fueron atendidos con esquemas de atención integral, 795 mil niños y niñas menores de 5 años se beneficiaron gracias a los Hogares Comunitarios de Bienestar. También cabe destacar los 20 mil agentes educativos formados en atención integral, 70 unidades de servicios con implementación de salas de lectura, 63 mil visitas de supervisión a las modalidades de Primera Infancia y los 77 Centros de Desarrollo Infantil entregados para operación.
En materia de protección, se enfatizó en la atención de 68.628 niños, niñas y adolescentes víctimas de desplazamiento forzado, acogidos a través de las 105 Unidades Móviles; 646 niños, niñas y adolescentes desvinculados; 476 huérfanos por causa del conflicto y a 139 niños, niñas y adolescentes víctimas de minas antipersona y artefactos explosivos. Gracias al proceso de adopción, se restableció el derecho a tener una familia a 1.082 niños, niñas y adolescentes, un 53% de ellos con características y necesidades especiales. Igualmente, 80 niños, niñas y adolescentes viajaron en el marco de la estrategia vacaciones en el extranjero y 38 con carta de intención. Igualmente, 12.266 adolescentes fueron atendidos el año pasado en el marco del Sistema Responsabilidad Penal para Adolescentes.
En materia de Nutrición, el ICBF brindó apoyo a 89.790 beneficiarios a través de la Estrategia de Recuperación Nutricional; 52.996 niños y niñas menores de 2 años con desnutrición y 19.534 mujeres gestantes y lactantes con bajo peso fueron beneficiarios de recuperación con énfasis en los primeros 1.000 días y 328.000 fueron beneficiarios del programa DIA. De otra parte, se destacó la atención a 35 mil familias beneficiadas del programa "Familias Afectivas", 37 mil familias atendidas con el programa "Territorios Étnicos con Bienestar", 1.340 familias en comunidades rurales y 1.028 familias en Innovación para la atención de familias y comunidades y 2.880 familias con el programa "UNAFAS".
En el marco de la atención a la población de niñez y adolescencia se remarcó la estrategia Generaciones con Bienestar donde se beneficiaron 200 mil niños y jóvenes, mientras que a través de la estrategia Prevención del Embarazo Adolescente, 3 mil niños, niñas y adolescentes estuvieron en proceso de formación, se adelantaron 115 acciones comunitarias, 934 agentes educativos fueron formados y 297 menores de edad de 18 municipios recibieron capacitación en participación significativa para la prevención del embarazo en la adolescencia. Por último, cabe destacar que con la iniciativa de Escuela de padres, madres, docentes y cuidadores, se atendieron 6.000 niños, niñas y adolescentes y fueron formados 1.500 padres, madres y cuidadores formados.
Unidad para las Víctimas
La Unidad para las Víctimas también entregó su balance de gestión durante 2015, año en el que fueron indemnizadas 106.001 personas llegando a un acumulado de 588.400 víctimas de la violencia que han recibido indemnización por diferentes hechos. En este último año la Unidad implementó la medición de superación de situación de vulnerabilidad, determinando que 33.946 víctimas superaron esa situación.
En 2015 se avanzó en la ruta de reparación colectiva con 303 sujetos de esta modalidad, de los cuales, 137 son comunidades no étnicas, 8 organizaciones de mujeres, 5 casos de incidencia nacional y 153 son comunidades étnicas, tres de los cuales ya concluyeron el proceso con la protocolización del Plan de Reparación Colectiva: Comunidad de Guacoche, Comunidad de Kitek Kiwe y el pueblo Rrom, de acuerdo con sus referentes culturales, ancestrales y comunitarios.
De igual manera se implementó la ruta de reparación integral específica con las mujeres víctimas de violencia sexual, en la cual participaron 1.118 mujeres generando espacios de confianza y empoderamiento para su incidencia en instancias de toma de decisión.
En cuanto a atención humanitaria, la Unidad de Víctimas acompañó el retorno y reubicación de 24.440 hogares y con atendió sicosocialmente a 34.091 víctimas en todo el país. Así mismo realizó el acompañamiento de 427 procesos de entrega de restos de víctimas de desaparición forzada.
Consolidación Territorial
Desde la Unidad Administrativa para la Consolidación Territorial, actualmente Dirección de Gestión Territorial de Prosperidad Social, en 2015 se invirtieron $137.000 millones en zonas afectadas por el conflicto y los cultivos ilícitos, de los cuales $67 mil millones se destinaron para apoyar a 8.740 familias que decidieron abandonar los cultivos de coca en 210 veredas de 40 municipios del país; así como para el fortalecimiento de 49 organizaciones de productores.
Con el propósito de lograr territorios libres de cultivos ilícitos y promover una cultura de la legalidad con miras hacia la construcción de la paz, se lograron erradicar 5.254 hectáreas de ilícitos a través de la estrategia de erradicación manual forzosa desarrollada por los Grupos Móviles de Erradicación – GME con un aporte de $49 mil millones.
Mediante el Programa de Respuesta Rápida que busca generar confianza entre las comunidades y el Estado, llevando soluciones a las necesidades apremiantes y priorizadas por las comunidades; se ejecutaron 115 proyectos con una inversión de $16 mil millones en obras de pequeña y mediana infraestructura, asistencia comunitaria y generación de ingresos, que se llevaron a 409 veredas de 61 municipios del país, e igualmente se fortalecieron 168 organizaciones sociales entre ellas, juntas de acción comunal, asociaciones de productores, resguardos indígenas, mujeres y juntas de hogares juveniles.
A través de la gestión interinstitucional de Consolidación Territorial, en 2015 se logró facilitar la articulación con diferentes actores públicos, privados y de cooperación internacional para la priorización y ejecución de nuevos proyectos de inversión por un total de recursos propios de $3 mil millones y de $ 67.914 millones apalancados, los cuales se invirtieron en acciones de fortalecimiento institucional, justicia, desarrollo social, cultura, educación, servicios financieros, cartografía, infraestructura en electrificación, agua, tecnológica y estructuración de proyectos.
Centro Nacional de Memoria Histórica
En su compromiso con la dignificación, reparación integral de las víctimas y el derecho a la verdad, el Centro Nacional de Memoria Histórica publicó el año anterior 15 informes de memoria histórica, finalizó 20 proyectos de reconstrucción de memoria e inició 5 nuevos proyectos de este tipo.
Además, documentó 55.000 hechos de violencia del conflicto armado y dispuso para consulta 60.800 documentos de archivo y colecciones sobre derechos humanos, con lo que aumentó a 160.048 los documentos que se encuentran disponibles para consultar, dentro de los que se encuentra el texto "Operación Cirirí – Familia Lalinde" reconocido como Patrimonio Documental UNESCO en octubre de 2015.
De igual manera, el Centro Nacional de Memoria Histórica adelantó el concurso público internacional para el diseño del Museo Nacional de la Memoria que tendrá un área de 14.178 metros cuadrados y estará ubicado en Bogotá. / May. 05, 2016. (Fotografía Oficial Prosperidad Social / Emilio Aparicio Rodríguez).
DPS Página Web / Twitter / Facebook / Youtube / Instagram
Der Bundestag will am 25. Juni 2014 die nächsten beiden Auslandseinsätze der Bundeswehr beschließen. Auf der Tagesordnung des Bundestages steht: „Fortsetzung der Beteiligung bewaffneter deutscher Streitkräfte an der Multidimensionalen Integrierten Stabilisierungsmission der Vereinten Nationen in Mali (MINUSMA)“ und „Fortsetzung der Beteiligung bewaffneter deutscher Streitkräfte an der "United Nations Interim Force in Lebanon" (UNIFIL)“.
Wir rufen auf, dagegen zu demonstrieren.
From left to right:
Adam Blackwell, OAS Secretary for Multidimensional Security
Toomas Vaks, Director of Cyber Security of the Government of Estonia
Date: October 20, 2014
Place: Washington, DC.
Credit: Juan Manuel Herrera/OAS
Secretary-General António Guterres speaks with Mahamat Saleh Annadif, Special Representative and Head of the United Nations Multidimensional Integrated Stabilization Mission in Mali (MINUSMA) at the airport where they will board on a UN plane to Mopti, Mali.
Peacekeepers serving with the UN Multidimensional Integrated Stabilization Mission in Mali (MINUSMA) secure the roads as the SG convoy drives by in Mopti, Mali.
La directora de Prosperidad Social, Tatyana Orozco de la Cruz, visitó Cúcuta y El Zulia en Norte de Santander donde hizo la entrega oficial de ocho obras que beneficiarán a la comunidad y permitirán continuar la labor de la Entidad en la lucha contra la erradicación de la pobreza multidimensional. Durante su visita, la Directora explicó las 5 claves +1 con las que Prosperidad Social trabajará en 2017 para lograr los planes establecidos en Norte de Santander.
"Con la entrega de estas obras, ratificamos nuestro compromiso con la población nortesantandereana. A través del Índice de Pobreza Multidimensional[1] hemos logrado identificar las mayores falencias en cada departamento y focalizar así nuestro trabajo durante 2017. En el caso de Norte de Santander lo haremos con la implementación de 5 claves +1" aseguró Tatyana Orozco, directora de Prosperidad Social.
En esta línea, la Directora describió las 5 claves + 1:
- Primera clave: Trabajo. Más de 2.800 personas se beneficiarán este año de los programas de generación de ingresos y, de hecho, durante 2016 cerca de 1.850 personas se vieron beneficiadas por cuenta de los programas de empleabilidad de la entidad tales como Mi Negocio y Empleo para la prosperidad. Todos estos esfuerzos apuntan a mitigar la brecha en materia de trabajo. De hecho, Cúcuta es la ciudad con más incentivos de Mi Negocio.
- Segunda clave: Educación. Más de 98 mil familias se beneficiarán de Más Familias en Acción, programa que incide positivamente en las condiciones educativas, de salud y de protección a la niñez y la juventud. Así mismo, más de 7 mil jóvenes del departamento se beneficiarán durante 2017 del programa Jóvenes en Acción que tiene como objetivo incentivar la educación de la población joven, en condición de pobreza y vulnerabilidad.
- Tercera clave: Vivienda. Se llevarán a cabo más de 6 mil mejoramientos de vivienda y se invertirán más de $42 mil millones de pesos en 50 proyectos de infraestructura social y de hábitat en el departamento.
- Cuarta clave: Salud. A través de Más Familias en Acción continuaremos incentivando y monitoreando la realización de controles médicos periódicos en los niños de las familias participantes del programa.
- Quinta clave: Niñez y juventud. La mayoría de nuestros programas busca llegar a los niños, adolescentes y jóvenes del departamento, es decir, tienen un enfoque especial en este segmento poblacional. Esto se une a la estrategia de Atención Integral a la Primera Infancia "De Cero a Siempre".
+1. Los programas de Prosperidad Social se ejecutan bajo parámetros y acuerdos de transparencia.
Entre los planes de la Entidad, además de trabajar bajo las dimensiones propuestas en el Índice de Pobreza Multidimensional, la clave estará en hacerlo bajo los estándares de transparencia. "En Prosperidad Social velamos porque todos nuestros proyectos y la ejecución de nuestros recursos sea comunicado de manera abierta a todos los ciudadanos, las autoridades y nuestros públicos de interés. Por esto, hemos compartido nuestros planes para 2017 en varios departamentos del país", concluyó Orozco.
Estas cinco claves ratifican el trabajo de la Entidad en la lucha contra la pobreza en el departamento donde tendremos una inversión total de $118 mil millones de pesos durante el 2017.
[1] El Índice de Pobreza Multidimensional fue creado por el Oxford Poverty & Human Development Initiative (OPHI) como un indicador que busca medir la pobreza desde una metodología multidimensional, e identificar las múltiples carencias a nivel de los hogares y las personas en los ámbitos de la salud, la educación y la calidad de vida. En Colombia, está basado en la evaluación de cinco dimensiones claves: las condiciones educativas del hogar, las condiciones de la niñez y la juventud, la salud, el trabajo y el acceso a los servicios públicos domiciliarios y el estado de la vivienda. / Feb. 21, 2017. (Fotografía Oficial Prosperidad Social / Emilio Aparicio Rodríguez).
Esta fotografía oficial del Departamento Administrativo para la Prosperidad Social está disponible sólo para ser publicada por las organizaciones de noticias, medios nacionales e internacionales y/o para uso personal de impresión por el sujeto de la fotografía. La fotografía no puede ser alterada digitalmente o manipularse de ninguna manera, y tampoco puede usarse en materiales comerciales o políticos, anuncios, correos electrónicos, productos o promociones que de cualquier manera sugieran aprobación por parte del Departamento Administrativo para la Prosperidad Social.
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Babacar Gaye, Special Representative of the Secretary-General in the Central African Republic and Head of the UN Multidimensional Integrated Stabilization Mission in the Central African Republic (MINUSCA) talks to Charles Malinas, Ambassador of France, before a meeting at the headquarters of the African-led International Support Mission to the Central African Republic (MISCA) in Bangui on 16 July 2014.
UN Photo/Catianne Tijerina
Farah Diva Urrutia, Secretary for Multidimensional Security
Date: April 8, 2019
Place: Washington DC
Credit: Juan Manuel Herrera/OAS
Der Bundestag will am 25. Juni 2014 die nächsten beiden Auslandseinsätze der Bundeswehr beschließen. Auf der Tagesordnung des Bundestages steht: „Fortsetzung der Beteiligung bewaffneter deutscher Streitkräfte an der Multidimensionalen Integrierten Stabilisierungsmission der Vereinten Nationen in Mali (MINUSMA)“ und „Fortsetzung der Beteiligung bewaffneter deutscher Streitkräfte an der "United Nations Interim Force in Lebanon" (UNIFIL)“.
Wir rufen auf, dagegen zu demonstrieren.
Diane Corner arrives in Bangui on 9 September 2014 to assume her new post as Deputy Special Representative (Political) of the Special Representative of the Secretary-General.
UN Photo/Catianne Tijerina
United Nations Police (UNPOL) Officers from Benin serving with the United Nations Multidimensional Integrated Stabilization Mission in Mali (MINUSMA) and Malian National Guard Officer conduct daily joint patrols in the streets of Gao, to ensure general security, maintain order and offer protection of civilians. They are escorted by Formed Police Unit (FPU) from the Burkina Faso Contingent. Photo MINUSMA/Marco Dormino
Members of United Nations Multidimensional Integrated Stabilization Mission in Mali (MINUSMA)'s Electoral team monitor a voting center in Bamako during the 2018 presidential elections. Photo MINUSMA/Marco Dormino
Security Officers of the UN Multidimensional Integrated Stabilization Mission in Mali (MINUSMA) coordinate the SG convoy on its way to the G5 Sahel Joint Force Headquarters in Mopti, Mali.
Designed By: Tomoko Fuse
Folded By: Stephen Jeppson
Construction Design By: Stephen Jeppson
Paper: Colored copy paper
Diagrams: Unit Origami: Multidimensional Transformations
Commissioned to work with SALT Research collections, artist Refik Anadol employed machine learning algorithms to search and sort relations among 1,700,000 documents. Interactions of the multidimensional data found in the archives are, in turn, translated into an immersive media installation. Archive Dreaming, which is presented as part of The Uses of Art: Final Exhibition with the support of the Culture Programme of the European Union, is user-driven; however, when idle, the installation "dreams" of unexpected correlations among documents. The resulting high-dimensional data and interactions are translated into an architectural immersive space.
Shortly after receiving the commission, Anadol was a resident artist for Google's Artists and Machine Intelligence Program where he closely collaborated with Mike Tyka and explored cutting-edge developments in the field of machine intelligence in an environment that brings together artists and engineers. Developed during this residency, his intervention Archive Dreaming transforms the gallery space on floor -1 at SALT Galata into an all-encompassing environment that intertwines history with the contemporary, and challenges immutable concepts of the archive, while destabilizing archive-related questions with machine learning algorithms.
In this project, a temporary immersive architectural space is created as a canvas with light and data applied as materials. This radical effort to deconstruct the framework of an illusory space will transgress the normal boundaries of the viewing experience of a library and the conventional flat cinema projection screen, into a three dimensional kinetic and architectonic space of an archive visualized with machine learning algorithms. By training a neural network with images of 1,700,000 documents at SALT Research the main idea is to create an immersive installation with architectural intelligence to reframe memory, history and culture in museum perception for 21st century through the lens of machine intelligence.
SALT is grateful to Google's Artists and Machine Intelligence program, and Doğuş Technology, ŠKODA, Volkswagen Doğuş Finansman for supporting Archive Dreaming.
Location : SALT Gatala, Istanbul, Turkey
Exhibition Dates : April 20 - June 11
6 Meters Wide Circular Architectural Installation
4 Channel Video, 8 Channel Audio
Custom Software, Media Server, Table for UI Interaction
For more information:
refikanadol.com/works/archive-dreaming/
La partecipazione politica è un fenomeno multidimensionale che si esprime a diversi livelli di partecipazione, istituzionalizzata e non, visibile e invisibile. Si prende parte alla vita politica in maniera manifesta quando si rappresenta il proprio punto di vista in prima persona, andando a comizi o cortei, organizzando forme di protesta, sostenendo un partito, un movimento, un’organizzazione finanziariamente o svolgendovi delle attività. Si partecipa alla vita politica anche quando, pur senza impegnarsi in maniera diretta e visibile, non si è indifferenti a quanto succede, quando ci s’informa, quando si parla o si discute di politica con gli altri. Spesso, infatti, l’interesse verso il mondo politico e la cosa pubblica non necessariamente si traduce in attività di sostegno alla politica in senso stretto o in attività con una chiara visibilità all’esterno. In questo caso la partecipazione si dice “invisibile”, tuttavia possono connotarsi anche hai margini della tipologia degli “indifferenti”.
Si prega di non utilizzare le mie immagini su siti web, blog o altri mezzi senza il mio permesso!
Please don't use my images on websites, blogs or other media without my permission!
Por favor, no use mis imágenes en los sitios web, blogs u otros medios de comunicación sin mi permiso!
SI CONSIGLIA LA VISIONE
41 militares da Força Aérea Portuguesa partiram no dia 12 de Janeiro de 2015 para o Mali, para integrarem a missão MINUSMA (United Nations Multidimensional Integrated Mission in Mali).
A cerimónia de partida teve lugar na Base Aérea N.º 6 (Montijo) e foi presidida pelo Chefe do Estado-Maior-General das Forças Armadas, General Artur Pina Monteiro, que fez questão de desejar sucesso aos militares da primeira missão Nacional fora do país em 2015. O Chefe do Estado-Maior da Força Aérea, General José António de Magalhães Araújo Pinheiro, também esteve na cerimónia e despediu-se pessoalmente de todos os seus homens.
A Força Nacional Destacada, composta por 47 elementos (41 da Força Aérea e seis do Exército), estará quatro meses neste país africano, sob a égide das Nações Unidas. O contingente é composto, para além dos militares, por uma aeronave C-295M da Esquadra 502 – “Elefantes”.
Moroccan peacekeepers serving with the UN Multidimensional Integrated Stabilization Mission in the Central African Republic (MINUSCA) in Bangui are deployed to Bambari on 15 June 2014.
UN Photo/Catianne Tijerina
Moroccan peacekeepers serving with the UN Multidimensional Integrated Stabilization Mission in the Central African Republic (MINUSCA) in Bangui are deployed to Bambari on 15 June 2014.
UN Photo/Catianne Tijerina
A Moroccan peacekeeper serving with the UN Multidimensional Integrated Stabilization Mission in the Central African Republic (MINUSCA) in Bangui waits to join a convoy to Bambari on 14 June 2014.
UN Photo/Catianne Tijerina
Abdoulaye Bathily, Special Representative of the Secretary-General for the United Nations for Central Africa addresses the press at arrival in the capital Bangui on 15 July 2014.
UN Photo/Catianne Tijerina
La directora de Prosperidad Social, Tatyana Orozco de la Cruz, visitó Cúcuta y El Zulia en Norte de Santander donde hizo la entrega oficial de ocho obras que beneficiarán a la comunidad y permitirán continuar la labor de la Entidad en la lucha contra la erradicación de la pobreza multidimensional. Durante su visita, la Directora explicó las 5 claves +1 con las que Prosperidad Social trabajará en 2017 para lograr los planes establecidos en Norte de Santander.
"Con la entrega de estas obras, ratificamos nuestro compromiso con la población nortesantandereana. A través del Índice de Pobreza Multidimensional[1] hemos logrado identificar las mayores falencias en cada departamento y focalizar así nuestro trabajo durante 2017. En el caso de Norte de Santander lo haremos con la implementación de 5 claves +1" aseguró Tatyana Orozco, directora de Prosperidad Social.
En esta línea, la Directora describió las 5 claves + 1:
- Primera clave: Trabajo. Más de 2.800 personas se beneficiarán este año de los programas de generación de ingresos y, de hecho, durante 2016 cerca de 1.850 personas se vieron beneficiadas por cuenta de los programas de empleabilidad de la entidad tales como Mi Negocio y Empleo para la prosperidad. Todos estos esfuerzos apuntan a mitigar la brecha en materia de trabajo. De hecho, Cúcuta es la ciudad con más incentivos de Mi Negocio.
- Segunda clave: Educación. Más de 98 mil familias se beneficiarán de Más Familias en Acción, programa que incide positivamente en las condiciones educativas, de salud y de protección a la niñez y la juventud. Así mismo, más de 7 mil jóvenes del departamento se beneficiarán durante 2017 del programa Jóvenes en Acción que tiene como objetivo incentivar la educación de la población joven, en condición de pobreza y vulnerabilidad.
- Tercera clave: Vivienda. Se llevarán a cabo más de 6 mil mejoramientos de vivienda y se invertirán más de $42 mil millones de pesos en 50 proyectos de infraestructura social y de hábitat en el departamento.
- Cuarta clave: Salud. A través de Más Familias en Acción continuaremos incentivando y monitoreando la realización de controles médicos periódicos en los niños de las familias participantes del programa.
- Quinta clave: Niñez y juventud. La mayoría de nuestros programas busca llegar a los niños, adolescentes y jóvenes del departamento, es decir, tienen un enfoque especial en este segmento poblacional. Esto se une a la estrategia de Atención Integral a la Primera Infancia "De Cero a Siempre".
+1. Los programas de Prosperidad Social se ejecutan bajo parámetros y acuerdos de transparencia.
Entre los planes de la Entidad, además de trabajar bajo las dimensiones propuestas en el Índice de Pobreza Multidimensional, la clave estará en hacerlo bajo los estándares de transparencia. "En Prosperidad Social velamos porque todos nuestros proyectos y la ejecución de nuestros recursos sea comunicado de manera abierta a todos los ciudadanos, las autoridades y nuestros públicos de interés. Por esto, hemos compartido nuestros planes para 2017 en varios departamentos del país", concluyó Orozco.
Estas cinco claves ratifican el trabajo de la Entidad en la lucha contra la pobreza en el departamento donde tendremos una inversión total de $118 mil millones de pesos durante el 2017.
[1] El Índice de Pobreza Multidimensional fue creado por el Oxford Poverty & Human Development Initiative (OPHI) como un indicador que busca medir la pobreza desde una metodología multidimensional, e identificar las múltiples carencias a nivel de los hogares y las personas en los ámbitos de la salud, la educación y la calidad de vida. En Colombia, está basado en la evaluación de cinco dimensiones claves: las condiciones educativas del hogar, las condiciones de la niñez y la juventud, la salud, el trabajo y el acceso a los servicios públicos domiciliarios y el estado de la vivienda. / Feb. 21, 2017. (Fotografía Oficial Prosperidad Social / Emilio Aparicio Rodríguez).
Esta fotografía oficial del Departamento Administrativo para la Prosperidad Social está disponible sólo para ser publicada por las organizaciones de noticias, medios nacionales e internacionales y/o para uso personal de impresión por el sujeto de la fotografía. La fotografía no puede ser alterada digitalmente o manipularse de ninguna manera, y tampoco puede usarse en materiales comerciales o políticos, anuncios, correos electrónicos, productos o promociones que de cualquier manera sugieran aprobación por parte del Departamento Administrativo para la Prosperidad Social.
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Aurélien Agbénonci, Deputy Special Representative of the Secretary-General and UN Resident Coordinator and UN Development Programme Resident Representative, speaks at a celebration held at the Assemblee Nationale in honor of World Humanitarian Day in Bangui on 19 August, 2014.
UN Photo/Catianne Tijerina
U.S., African and European military personnel stand in formation during the closing ceremony for Western Accord 15, at Winkelman Kazerne, Harskamp, Netherlands, July 31. Western Accord 2015 replicates the Multidimensional Integrated Stabilization Mission in Mali, Sector Headquarters mission command in support of United Nation and African Union mandated peacekeeping operations. (U.S. Army Africa photo by Sgt. Marcus Fichtl)
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