Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.

The developing testis provides an environment that nurtures germ cell development, ultimately ensuring spermatogenesis and fertility. Impacts on this environment are considered to underlie aberrant germ cell development and formation of germ cell tumour precursors. The signaling events involved in t...

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Published in:PLoS ONE
Main Authors: Denise C Miles, Stephanie I Wakeling, Jessica M Stringer, Jocelyn A van den Bergen, Dagmar Wilhelm, Andrew H Sinclair, Patrick S Western
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Online Access:http://europepmc.org/articles/PMC3546992?pdf=render
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author Denise C Miles
Stephanie I Wakeling
Jessica M Stringer
Jocelyn A van den Bergen
Dagmar Wilhelm
Andrew H Sinclair
Patrick S Western
author_facet Denise C Miles
Stephanie I Wakeling
Jessica M Stringer
Jocelyn A van den Bergen
Dagmar Wilhelm
Andrew H Sinclair
Patrick S Western
author_sort Denise C Miles
collection DOAJ
container_title PLoS ONE
description The developing testis provides an environment that nurtures germ cell development, ultimately ensuring spermatogenesis and fertility. Impacts on this environment are considered to underlie aberrant germ cell development and formation of germ cell tumour precursors. The signaling events involved in testis formation and male fetal germ cell development remain largely unknown. Analysis of knockout mice lacking single Tgfβ family members has indicated that Tgfβ's are not required for sex determination. However, due to functional redundancy, it is possible that additional functions for these ligands in gonad development remain to be discovered. Using FACS purified gonadal cells, in this study we show that the genes encoding Activin's, TGFβ's, Nodal and their respective receptors, are expressed in sex and cell type specific patterns suggesting particular roles in testis and germ cell development. Inhibition of signaling through the receptors ALK4, ALK5 and ALK7, and ALK5 alone, demonstrated that TGFβ signaling is required for testis cord formation during the critical testis-determining period. We also show that signaling through the Activin/NODAL receptors, ALK4 and ALK7 is required for promoting differentiation of male germ cells and their entry into mitotic arrest. Finally, our data demonstrate that Nodal is specifically expressed in male germ cells and expression of the key pluripotency gene, Nanog was significantly reduced when signaling through ALK4/5/7 was blocked. Our strategy of inhibiting multiple Activin/NODAL/TGFβ receptors reduces the functional redundancy between these signaling pathways, thereby revealing new and essential roles for TGFβ and Activin signaling during testis formation and male germ cell development.
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spelling doaj-art-e7f2b59458ea4d6b968f5ba8f98802d42025-08-19T19:33:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5460610.1371/journal.pone.0054606Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.Denise C MilesStephanie I WakelingJessica M StringerJocelyn A van den BergenDagmar WilhelmAndrew H SinclairPatrick S WesternThe developing testis provides an environment that nurtures germ cell development, ultimately ensuring spermatogenesis and fertility. Impacts on this environment are considered to underlie aberrant germ cell development and formation of germ cell tumour precursors. The signaling events involved in testis formation and male fetal germ cell development remain largely unknown. Analysis of knockout mice lacking single Tgfβ family members has indicated that Tgfβ's are not required for sex determination. However, due to functional redundancy, it is possible that additional functions for these ligands in gonad development remain to be discovered. Using FACS purified gonadal cells, in this study we show that the genes encoding Activin's, TGFβ's, Nodal and their respective receptors, are expressed in sex and cell type specific patterns suggesting particular roles in testis and germ cell development. Inhibition of signaling through the receptors ALK4, ALK5 and ALK7, and ALK5 alone, demonstrated that TGFβ signaling is required for testis cord formation during the critical testis-determining period. We also show that signaling through the Activin/NODAL receptors, ALK4 and ALK7 is required for promoting differentiation of male germ cells and their entry into mitotic arrest. Finally, our data demonstrate that Nodal is specifically expressed in male germ cells and expression of the key pluripotency gene, Nanog was significantly reduced when signaling through ALK4/5/7 was blocked. Our strategy of inhibiting multiple Activin/NODAL/TGFβ receptors reduces the functional redundancy between these signaling pathways, thereby revealing new and essential roles for TGFβ and Activin signaling during testis formation and male germ cell development.http://europepmc.org/articles/PMC3546992?pdf=render
spellingShingle Denise C Miles
Stephanie I Wakeling
Jessica M Stringer
Jocelyn A van den Bergen
Dagmar Wilhelm
Andrew H Sinclair
Patrick S Western
Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.
title Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.
title_full Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.
title_fullStr Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.
title_full_unstemmed Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.
title_short Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development.
title_sort signaling through the tgf beta activin receptors alk4 5 7 regulates testis formation and male germ cell development
url http://europepmc.org/articles/PMC3546992?pdf=render
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