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Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis
Protein phosphatase 6 (PP6) is a member of the PP2A-like subfamily, which plays significant roles in numerous fundamental biological activities. We found that PPP6C plays important roles in male germ cells recently. Spermatogenesis is supported by the Sertoli cells in the seminiferous epithelium. In...
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/PMC8476514/ https://www.ncbi.nlm.nih.gov/pubmed/34580275 http://dx.doi.org/10.1038/s41419-021-04172-y |
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author | Lei, Wen-Long Li, Yuan-Yuan Meng, Tie-Gang Ning, Yan Sun, Si-Min Zhang, Chun-Hui Gui, Yaoting Wang, Zhen-Bo Qian, Wei-Ping Sun, Qing-Yuan |
author_facet | Lei, Wen-Long Li, Yuan-Yuan Meng, Tie-Gang Ning, Yan Sun, Si-Min Zhang, Chun-Hui Gui, Yaoting Wang, Zhen-Bo Qian, Wei-Ping Sun, Qing-Yuan |
author_sort | Lei, Wen-Long |
collection | PubMed |
description | Protein phosphatase 6 (PP6) is a member of the PP2A-like subfamily, which plays significant roles in numerous fundamental biological activities. We found that PPP6C plays important roles in male germ cells recently. Spermatogenesis is supported by the Sertoli cells in the seminiferous epithelium. In this study, we crossed Ppp6c(F/F) mice with AMH-Cre mice to gain mutant mice with specific depletion of the Ppp6c gene in the Sertoli cells. We discovered that the PPP6C cKO male mice were absolutely infertile and germ cells were largely lost during spermatogenesis. By combing phosphoproteome with bioinformatics analysis, we showed that the phosphorylation status of β-catenin at S552 (a marker of adherens junctions) was significantly upregulated in mutant mice. Abnormal β-catenin accumulation resulted in impaired testicular junction integrity, thus led to abnormal structure and functions of BTB. Taken together, our study reveals a novel function for PPP6C in male germ cell survival and differentiation by regulating the cell-cell communication through dephosphorylating β-catenin at S552. |
format | Online Article Text |
id | pubmed-8476514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84765142021-10-08 Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis Lei, Wen-Long Li, Yuan-Yuan Meng, Tie-Gang Ning, Yan Sun, Si-Min Zhang, Chun-Hui Gui, Yaoting Wang, Zhen-Bo Qian, Wei-Ping Sun, Qing-Yuan Cell Death Dis Article Protein phosphatase 6 (PP6) is a member of the PP2A-like subfamily, which plays significant roles in numerous fundamental biological activities. We found that PPP6C plays important roles in male germ cells recently. Spermatogenesis is supported by the Sertoli cells in the seminiferous epithelium. In this study, we crossed Ppp6c(F/F) mice with AMH-Cre mice to gain mutant mice with specific depletion of the Ppp6c gene in the Sertoli cells. We discovered that the PPP6C cKO male mice were absolutely infertile and germ cells were largely lost during spermatogenesis. By combing phosphoproteome with bioinformatics analysis, we showed that the phosphorylation status of β-catenin at S552 (a marker of adherens junctions) was significantly upregulated in mutant mice. Abnormal β-catenin accumulation resulted in impaired testicular junction integrity, thus led to abnormal structure and functions of BTB. Taken together, our study reveals a novel function for PPP6C in male germ cell survival and differentiation by regulating the cell-cell communication through dephosphorylating β-catenin at S552. Nature Publishing Group UK 2021-09-27 /pmc/articles/PMC8476514/ /pubmed/34580275 http://dx.doi.org/10.1038/s41419-021-04172-y 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 Lei, Wen-Long Li, Yuan-Yuan Meng, Tie-Gang Ning, Yan Sun, Si-Min Zhang, Chun-Hui Gui, Yaoting Wang, Zhen-Bo Qian, Wei-Ping Sun, Qing-Yuan Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis |
title | Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis |
title_full | Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis |
title_fullStr | Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis |
title_full_unstemmed | Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis |
title_short | Specific deletion of protein phosphatase 6 catalytic subunit in Sertoli cells leads to disruption of spermatogenesis |
title_sort | specific deletion of protein phosphatase 6 catalytic subunit in sertoli cells leads to disruption of spermatogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476514/ https://www.ncbi.nlm.nih.gov/pubmed/34580275 http://dx.doi.org/10.1038/s41419-021-04172-y |
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