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Sex biased human thymic architecture guides T cell development through spatially defined niches
Within the thymus, regulation of the cellular cross-talk directing T cell development is dependent on spatial interactions within specialized niches. To create a holistic, spatially defined map of tissue niches guiding postnatal T cell development we employed the multidimensional imaging platform CO...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120731/ https://www.ncbi.nlm.nih.gov/pubmed/37090676 http://dx.doi.org/10.1101/2023.04.13.536804 |
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author | Stankiewicz, Laura N Salim, Kevin Flaschner, Emily A Wang, Yu Xin Edgar, John M Lin, Bruce ZB Bingham, Grace C Major, Matthew C Jones, Ross D Blau, Helen M Rideout, Elizabeth J Levings, Megan K Zandstra, Peter W Rossi, Fabio MV |
author_facet | Stankiewicz, Laura N Salim, Kevin Flaschner, Emily A Wang, Yu Xin Edgar, John M Lin, Bruce ZB Bingham, Grace C Major, Matthew C Jones, Ross D Blau, Helen M Rideout, Elizabeth J Levings, Megan K Zandstra, Peter W Rossi, Fabio MV |
author_sort | Stankiewicz, Laura N |
collection | PubMed |
description | Within the thymus, regulation of the cellular cross-talk directing T cell development is dependent on spatial interactions within specialized niches. To create a holistic, spatially defined map of tissue niches guiding postnatal T cell development we employed the multidimensional imaging platform CO-detection by indEXing (CODEX), as well as CITE-seq and ATAC-seq. We generated age-matched 4–5-month-old postnatal thymus datasets for male and female donors, and identify significant sex differences in both T cell and thymus biology. We demonstrate a crucial role for JAG ligands in directing thymic-like dendritic cell development, reveal important functions of a novel population of ECM(−) fibroblasts, and characterize the medullary niches surrounding Hassall’s corpuscles. Together, these data represent a unique age-matched spatial multiomic resource to investigate how sex-based differences in thymus regulation and T cell development arise, and provide an essential resource to understand the mechanisms underlying immune function and dysfunction in males and females. |
format | Online Article Text |
id | pubmed-10120731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101207312023-04-22 Sex biased human thymic architecture guides T cell development through spatially defined niches Stankiewicz, Laura N Salim, Kevin Flaschner, Emily A Wang, Yu Xin Edgar, John M Lin, Bruce ZB Bingham, Grace C Major, Matthew C Jones, Ross D Blau, Helen M Rideout, Elizabeth J Levings, Megan K Zandstra, Peter W Rossi, Fabio MV bioRxiv Article Within the thymus, regulation of the cellular cross-talk directing T cell development is dependent on spatial interactions within specialized niches. To create a holistic, spatially defined map of tissue niches guiding postnatal T cell development we employed the multidimensional imaging platform CO-detection by indEXing (CODEX), as well as CITE-seq and ATAC-seq. We generated age-matched 4–5-month-old postnatal thymus datasets for male and female donors, and identify significant sex differences in both T cell and thymus biology. We demonstrate a crucial role for JAG ligands in directing thymic-like dendritic cell development, reveal important functions of a novel population of ECM(−) fibroblasts, and characterize the medullary niches surrounding Hassall’s corpuscles. Together, these data represent a unique age-matched spatial multiomic resource to investigate how sex-based differences in thymus regulation and T cell development arise, and provide an essential resource to understand the mechanisms underlying immune function and dysfunction in males and females. Cold Spring Harbor Laboratory 2023-04-16 /pmc/articles/PMC10120731/ /pubmed/37090676 http://dx.doi.org/10.1101/2023.04.13.536804 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Stankiewicz, Laura N Salim, Kevin Flaschner, Emily A Wang, Yu Xin Edgar, John M Lin, Bruce ZB Bingham, Grace C Major, Matthew C Jones, Ross D Blau, Helen M Rideout, Elizabeth J Levings, Megan K Zandstra, Peter W Rossi, Fabio MV Sex biased human thymic architecture guides T cell development through spatially defined niches |
title | Sex biased human thymic architecture guides T cell development through spatially defined niches |
title_full | Sex biased human thymic architecture guides T cell development through spatially defined niches |
title_fullStr | Sex biased human thymic architecture guides T cell development through spatially defined niches |
title_full_unstemmed | Sex biased human thymic architecture guides T cell development through spatially defined niches |
title_short | Sex biased human thymic architecture guides T cell development through spatially defined niches |
title_sort | sex biased human thymic architecture guides t cell development through spatially defined niches |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120731/ https://www.ncbi.nlm.nih.gov/pubmed/37090676 http://dx.doi.org/10.1101/2023.04.13.536804 |
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