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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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