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Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions
A growing body of evidence demonstrates that fetal-derived tissue-resident macrophages have developmental functions. It has been proposed that macrophages promote testicular functions, but which macrophage populations are involved is unclear. Previous studies showed that macrophages play critical ro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017703/ https://www.ncbi.nlm.nih.gov/pubmed/36922518 http://dx.doi.org/10.1038/s41467-023-37199-0 |
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author | Gu, Xiaowei Heinrich, Anna Li, Shu-Yun DeFalco, Tony |
author_facet | Gu, Xiaowei Heinrich, Anna Li, Shu-Yun DeFalco, Tony |
author_sort | Gu, Xiaowei |
collection | PubMed |
description | A growing body of evidence demonstrates that fetal-derived tissue-resident macrophages have developmental functions. It has been proposed that macrophages promote testicular functions, but which macrophage populations are involved is unclear. Previous studies showed that macrophages play critical roles in fetal testis morphogenesis and described two adult testicular macrophage populations, interstitial and peritubular. There has been debate regarding the hematopoietic origins of testicular macrophages and whether distinct macrophage populations promote specific testicular functions. Here our hematopoietic lineage-tracing studies in mice show that yolk-sac-derived macrophages comprise the earliest testicular macrophages, while fetal hematopoietic stem cells (HSCs) generate monocytes that colonize the gonad during a narrow time window in a Sertoli-cell-dependent manner and differentiate into adult testicular macrophages. Finally, we show that yolk-sac-derived versus HSC-derived macrophages have distinct functions during testis morphogenesis, while interstitial macrophages specifically promote adult Leydig cell steroidogenesis. Our findings provide insight into testicular macrophage origins and their tissue-specific roles. |
format | Online Article Text |
id | pubmed-10017703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100177032023-03-17 Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions Gu, Xiaowei Heinrich, Anna Li, Shu-Yun DeFalco, Tony Nat Commun Article A growing body of evidence demonstrates that fetal-derived tissue-resident macrophages have developmental functions. It has been proposed that macrophages promote testicular functions, but which macrophage populations are involved is unclear. Previous studies showed that macrophages play critical roles in fetal testis morphogenesis and described two adult testicular macrophage populations, interstitial and peritubular. There has been debate regarding the hematopoietic origins of testicular macrophages and whether distinct macrophage populations promote specific testicular functions. Here our hematopoietic lineage-tracing studies in mice show that yolk-sac-derived macrophages comprise the earliest testicular macrophages, while fetal hematopoietic stem cells (HSCs) generate monocytes that colonize the gonad during a narrow time window in a Sertoli-cell-dependent manner and differentiate into adult testicular macrophages. Finally, we show that yolk-sac-derived versus HSC-derived macrophages have distinct functions during testis morphogenesis, while interstitial macrophages specifically promote adult Leydig cell steroidogenesis. Our findings provide insight into testicular macrophage origins and their tissue-specific roles. Nature Publishing Group UK 2023-03-15 /pmc/articles/PMC10017703/ /pubmed/36922518 http://dx.doi.org/10.1038/s41467-023-37199-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Gu, Xiaowei Heinrich, Anna Li, Shu-Yun DeFalco, Tony Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
title | Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
title_full | Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
title_fullStr | Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
title_full_unstemmed | Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
title_short | Testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
title_sort | testicular macrophages are recruited during a narrow fetal time window and promote organ-specific developmental functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017703/ https://www.ncbi.nlm.nih.gov/pubmed/36922518 http://dx.doi.org/10.1038/s41467-023-37199-0 |
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