Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling

Androgen receptor (AR) signaling is essential for maintaining spermatogenesis and male fertility. However, the molecular mechanisms by which AR acts between male germ cells and somatic cells during spermatogenesis have not begun to be revealed until recently. With the advances obtained from the use...

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Autores principales: Congcong Cao, Qian Ma, Shaomei Mo, Ge Shu, Qunlong Liu, Jing Ye, Yaoting Gui
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Lenguaje:EN
Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/807224fc1ec445e8a3b5929880368353
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spelling oai:doaj.org-article:807224fc1ec445e8a3b59298803683532021-11-15T05:58:05ZSingle-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling2296-634X10.3389/fcell.2021.763267https://doaj.org/article/807224fc1ec445e8a3b59298803683532021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.763267/fullhttps://doaj.org/toc/2296-634XAndrogen receptor (AR) signaling is essential for maintaining spermatogenesis and male fertility. However, the molecular mechanisms by which AR acts between male germ cells and somatic cells during spermatogenesis have not begun to be revealed until recently. With the advances obtained from the use of transgenic mice lacking AR in Sertoli cells (SCARKO) and single-cell transcriptomic sequencing (scRNA-seq), the cell specific targets of AR action as well as the genes and signaling pathways that are regulated by AR are being identified. In this study, we collected scRNA-seq data from wild-type (WT) and SCARKO mice testes at p20 and identified four somatic cell populations and two male germ cell populations. Further analysis identified that the distribution of Sertoli cells was completely different and uncovered the cellular heterogeneity and transcriptional changes between WT and SCARKO Sertoli cells. In addition, several differentially expressed genes (DEGs) in SCARKO Sertoli cells, many of which have been previously implicated in cell cycle, apoptosis and male infertility, have also been identified. Together, our research explores a novel perspective on the changes in the transcription level of various cell types between WT and SCARKO mice testes, providing new insights for the investigations of the molecular and cellular processes regulated by AR signaling in Sertoli cells.Congcong CaoQian MaShaomei MoGe ShuQunlong LiuJing YeYaoting GuiFrontiers Media S.A.articlespermatogenesisARscRNA-seqmale infertilityknockoutBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic spermatogenesis
AR
scRNA-seq
male infertility
knockout
Biology (General)
QH301-705.5
spellingShingle spermatogenesis
AR
scRNA-seq
male infertility
knockout
Biology (General)
QH301-705.5
Congcong Cao
Qian Ma
Shaomei Mo
Ge Shu
Qunlong Liu
Jing Ye
Yaoting Gui
Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling
description Androgen receptor (AR) signaling is essential for maintaining spermatogenesis and male fertility. However, the molecular mechanisms by which AR acts between male germ cells and somatic cells during spermatogenesis have not begun to be revealed until recently. With the advances obtained from the use of transgenic mice lacking AR in Sertoli cells (SCARKO) and single-cell transcriptomic sequencing (scRNA-seq), the cell specific targets of AR action as well as the genes and signaling pathways that are regulated by AR are being identified. In this study, we collected scRNA-seq data from wild-type (WT) and SCARKO mice testes at p20 and identified four somatic cell populations and two male germ cell populations. Further analysis identified that the distribution of Sertoli cells was completely different and uncovered the cellular heterogeneity and transcriptional changes between WT and SCARKO Sertoli cells. In addition, several differentially expressed genes (DEGs) in SCARKO Sertoli cells, many of which have been previously implicated in cell cycle, apoptosis and male infertility, have also been identified. Together, our research explores a novel perspective on the changes in the transcription level of various cell types between WT and SCARKO mice testes, providing new insights for the investigations of the molecular and cellular processes regulated by AR signaling in Sertoli cells.
format article
author Congcong Cao
Qian Ma
Shaomei Mo
Ge Shu
Qunlong Liu
Jing Ye
Yaoting Gui
author_facet Congcong Cao
Qian Ma
Shaomei Mo
Ge Shu
Qunlong Liu
Jing Ye
Yaoting Gui
author_sort Congcong Cao
title Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling
title_short Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling
title_full Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling
title_fullStr Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling
title_full_unstemmed Single-Cell RNA Sequencing Defines the Regulation of Spermatogenesis by Sertoli-Cell Androgen Signaling
title_sort single-cell rna sequencing defines the regulation of spermatogenesis by sertoli-cell androgen signaling
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/807224fc1ec445e8a3b5929880368353
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