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TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice
Testicular development and function rely on interactions between somatic cells and the germline, but similar to other organs, regenerative capacity declines in aging and disease. Whether the adult testis maintains a reserve progenitor population remains uncertain. Here, we characterize a recently id...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222243/ https://www.ncbi.nlm.nih.gov/pubmed/34162856 http://dx.doi.org/10.1038/s41467-021-24130-8 |
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author | Shen, Yu-chi Shami, Adrienne Niederriter Moritz, Lindsay Larose, Hailey Manske, Gabriel L. Ma, Qianyi Zheng, Xianing Sukhwani, Meena Czerwinski, Michael Sultan, Caleb Chen, Haolin Gurczynski, Stephen J. Spence, Jason R. Orwig, Kyle E. Tallquist, Michelle Li, Jun Z. Hammoud, Saher Sue |
author_facet | Shen, Yu-chi Shami, Adrienne Niederriter Moritz, Lindsay Larose, Hailey Manske, Gabriel L. Ma, Qianyi Zheng, Xianing Sukhwani, Meena Czerwinski, Michael Sultan, Caleb Chen, Haolin Gurczynski, Stephen J. Spence, Jason R. Orwig, Kyle E. Tallquist, Michelle Li, Jun Z. Hammoud, Saher Sue |
author_sort | Shen, Yu-chi |
collection | PubMed |
description | Testicular development and function rely on interactions between somatic cells and the germline, but similar to other organs, regenerative capacity declines in aging and disease. Whether the adult testis maintains a reserve progenitor population remains uncertain. Here, we characterize a recently identified mouse testis interstitial population expressing the transcription factor Tcf21. We found that TCF21(lin) cells are bipotential somatic progenitors present in fetal testis and ovary, maintain adult testis homeostasis during aging, and act as potential reserve somatic progenitors following injury. In vitro, TCF21(lin) cells are multipotent mesenchymal progenitors which form multiple somatic lineages including Leydig and myoid cells. Additionally, TCF21(+) cells resemble resident fibroblast populations reported in other organs having roles in tissue homeostasis, fibrosis, and regeneration. Our findings reveal that the testis, like other organs, maintains multipotent mesenchymal progenitors that can be potentially leveraged in development of future therapies for hypoandrogenism and/or infertility. |
format | Online Article Text |
id | pubmed-8222243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82222432021-07-09 TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice Shen, Yu-chi Shami, Adrienne Niederriter Moritz, Lindsay Larose, Hailey Manske, Gabriel L. Ma, Qianyi Zheng, Xianing Sukhwani, Meena Czerwinski, Michael Sultan, Caleb Chen, Haolin Gurczynski, Stephen J. Spence, Jason R. Orwig, Kyle E. Tallquist, Michelle Li, Jun Z. Hammoud, Saher Sue Nat Commun Article Testicular development and function rely on interactions between somatic cells and the germline, but similar to other organs, regenerative capacity declines in aging and disease. Whether the adult testis maintains a reserve progenitor population remains uncertain. Here, we characterize a recently identified mouse testis interstitial population expressing the transcription factor Tcf21. We found that TCF21(lin) cells are bipotential somatic progenitors present in fetal testis and ovary, maintain adult testis homeostasis during aging, and act as potential reserve somatic progenitors following injury. In vitro, TCF21(lin) cells are multipotent mesenchymal progenitors which form multiple somatic lineages including Leydig and myoid cells. Additionally, TCF21(+) cells resemble resident fibroblast populations reported in other organs having roles in tissue homeostasis, fibrosis, and regeneration. Our findings reveal that the testis, like other organs, maintains multipotent mesenchymal progenitors that can be potentially leveraged in development of future therapies for hypoandrogenism and/or infertility. Nature Publishing Group UK 2021-06-23 /pmc/articles/PMC8222243/ /pubmed/34162856 http://dx.doi.org/10.1038/s41467-021-24130-8 Text en © The Author(s) 2021 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 Shen, Yu-chi Shami, Adrienne Niederriter Moritz, Lindsay Larose, Hailey Manske, Gabriel L. Ma, Qianyi Zheng, Xianing Sukhwani, Meena Czerwinski, Michael Sultan, Caleb Chen, Haolin Gurczynski, Stephen J. Spence, Jason R. Orwig, Kyle E. Tallquist, Michelle Li, Jun Z. Hammoud, Saher Sue TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
title | TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
title_full | TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
title_fullStr | TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
title_full_unstemmed | TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
title_short | TCF21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
title_sort | tcf21(+) mesenchymal cells contribute to testis somatic cell development, homeostasis, and regeneration in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8222243/ https://www.ncbi.nlm.nih.gov/pubmed/34162856 http://dx.doi.org/10.1038/s41467-021-24130-8 |
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