Cargando…

Regulation of meiotic progression by Sertoli-cell androgen signaling

Androgen receptor (AR) signaling in Sertoli cells is known to be important for germ-cell progression through meiosis, but the extent to which androgens indirectly regulate specific meiotic stages is not known. Here, we combine synchronization of spermatogenesis, cytological analyses and single-cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Larose, Hailey, Kent, Travis, Ma, Qianyi, Shami, Adrienne Niederriter, Harerimana, Nadia, Li, Jun Z., Hammoud, Saher Sue, Handel, Mary Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851862/
https://www.ncbi.nlm.nih.gov/pubmed/33026960
http://dx.doi.org/10.1091/mbc.E20-05-0334
_version_ 1783645705819127808
author Larose, Hailey
Kent, Travis
Ma, Qianyi
Shami, Adrienne Niederriter
Harerimana, Nadia
Li, Jun Z.
Hammoud, Saher Sue
Handel, Mary Ann
author_facet Larose, Hailey
Kent, Travis
Ma, Qianyi
Shami, Adrienne Niederriter
Harerimana, Nadia
Li, Jun Z.
Hammoud, Saher Sue
Handel, Mary Ann
author_sort Larose, Hailey
collection PubMed
description Androgen receptor (AR) signaling in Sertoli cells is known to be important for germ-cell progression through meiosis, but the extent to which androgens indirectly regulate specific meiotic stages is not known. Here, we combine synchronization of spermatogenesis, cytological analyses and single-cell RNAseq (scRNAseq) in the Sertoli-cell androgen receptor knockout (SCARKO) mutant and control mice, and demonstrate that SCARKO mutant spermatocytes exhibited normal expression and localization of key protein markers of meiotic prophase events, indicating that initiation of meiotic prophase is not androgen dependent. However, spermatocytes from SCARKO testes failed to acquire competence for the meiotic division phase. ScRNAseq analysis of wild-type and SCARKO mutant testes revealed a molecular transcriptomic block in an early meiotic prophase state (leptotene/zygotene) in mutant germ cells, and identified several misregulated genes in SCARKO Sertoli cells, many of which have been previously implicated in male infertility. Together, our coordinated cytological and scRNAseq analyses identified germ-cell intrinsic and extrinsic genes responsive to Sertoli-cell androgen signaling that promotes cellular states permissive for the meiotic division phase.
format Online
Article
Text
id pubmed-7851862
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The American Society for Cell Biology
record_format MEDLINE/PubMed
spelling pubmed-78518622021-02-18 Regulation of meiotic progression by Sertoli-cell androgen signaling Larose, Hailey Kent, Travis Ma, Qianyi Shami, Adrienne Niederriter Harerimana, Nadia Li, Jun Z. Hammoud, Saher Sue Handel, Mary Ann Mol Biol Cell Articles Androgen receptor (AR) signaling in Sertoli cells is known to be important for germ-cell progression through meiosis, but the extent to which androgens indirectly regulate specific meiotic stages is not known. Here, we combine synchronization of spermatogenesis, cytological analyses and single-cell RNAseq (scRNAseq) in the Sertoli-cell androgen receptor knockout (SCARKO) mutant and control mice, and demonstrate that SCARKO mutant spermatocytes exhibited normal expression and localization of key protein markers of meiotic prophase events, indicating that initiation of meiotic prophase is not androgen dependent. However, spermatocytes from SCARKO testes failed to acquire competence for the meiotic division phase. ScRNAseq analysis of wild-type and SCARKO mutant testes revealed a molecular transcriptomic block in an early meiotic prophase state (leptotene/zygotene) in mutant germ cells, and identified several misregulated genes in SCARKO Sertoli cells, many of which have been previously implicated in male infertility. Together, our coordinated cytological and scRNAseq analyses identified germ-cell intrinsic and extrinsic genes responsive to Sertoli-cell androgen signaling that promotes cellular states permissive for the meiotic division phase. The American Society for Cell Biology 2020-12-01 /pmc/articles/PMC7851862/ /pubmed/33026960 http://dx.doi.org/10.1091/mbc.E20-05-0334 Text en © 2020 Larose et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Larose, Hailey
Kent, Travis
Ma, Qianyi
Shami, Adrienne Niederriter
Harerimana, Nadia
Li, Jun Z.
Hammoud, Saher Sue
Handel, Mary Ann
Regulation of meiotic progression by Sertoli-cell androgen signaling
title Regulation of meiotic progression by Sertoli-cell androgen signaling
title_full Regulation of meiotic progression by Sertoli-cell androgen signaling
title_fullStr Regulation of meiotic progression by Sertoli-cell androgen signaling
title_full_unstemmed Regulation of meiotic progression by Sertoli-cell androgen signaling
title_short Regulation of meiotic progression by Sertoli-cell androgen signaling
title_sort regulation of meiotic progression by sertoli-cell androgen signaling
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851862/
https://www.ncbi.nlm.nih.gov/pubmed/33026960
http://dx.doi.org/10.1091/mbc.E20-05-0334
work_keys_str_mv AT larosehailey regulationofmeioticprogressionbysertolicellandrogensignaling
AT kenttravis regulationofmeioticprogressionbysertolicellandrogensignaling
AT maqianyi regulationofmeioticprogressionbysertolicellandrogensignaling
AT shamiadrienneniederriter regulationofmeioticprogressionbysertolicellandrogensignaling
AT harerimananadia regulationofmeioticprogressionbysertolicellandrogensignaling
AT lijunz regulationofmeioticprogressionbysertolicellandrogensignaling
AT hammoudsahersue regulationofmeioticprogressionbysertolicellandrogensignaling
AT handelmaryann regulationofmeioticprogressionbysertolicellandrogensignaling