| Literature DB >> 34162856 |
Yu-Chi Shen1, Adrienne Niederriter Shami1, Lindsay Moritz2, Hailey Larose1, Gabriel L Manske2, Qianyi Ma1, Xianing Zheng1, Meena Sukhwani3, Michael Czerwinski4, Caleb Sultan1, Haolin Chen5, Stephen J Gurczynski4, Jason R Spence4, Kyle E Orwig3, Michelle Tallquist6, Jun Z Li1,7, Saher Sue Hammoud8,9,10.
Abstract
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 TCF21lin 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, TCF21lin 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.Entities:
Year: 2021 PMID: 34162856 DOI: 10.1038/s41467-021-24130-8
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919