Sertoli cell differentiation is induced both cell-autonomously and through prostaglandin signaling during mammalian sex determination

被引:217
作者
Wilhelm, D
Martinson, F
Bradford, S
Wilson, MJ
Combes, AN
Beverdam, A
Bowles, J
Mizusaki, H
Koopman, P [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Div Mol Genet & Dev, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Inst Mol Biosci, ARC Ctr Excellence Biotechnol & Dev, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
SRY; Sox9; gonad development; sex determination; testis differentiation; prostaglandin; sertoli cell;
D O I
10.1016/j.ydbio.2005.08.039
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have raised an antibody specifically recognizing endogenous mouse SRY protein and used it to investigate the molecular and cellular mode of action of SRY in testis determination. We find that expression of SRY protein closely mirrors the expression of Sry mRNA in Mouse genital ridges and is detectable for 6 to 8 h after the mRNA ceases to be detectable. The subset of somatic cells that expresses SRY begins to express SOX9 almost immediately. Since these SOX9-positive cells go oil to develop as Sertoli cells, it appears that SRY expression marks the pre-Sertoli cell lineage and leads to up-regulation of Sox9 expression cell-autonomously. However, a small proportion of SOX9-positive cells did not appear to express SRY, possibly reflecting the additional involvement of paracrine signaling in activating Sox9 transcription in these cells. We confirmed by ex vivo cell mixing experiments that SRY is able to engage receptor-mediated signaling to up-regulate Sox9 expression. Finally, we showed by employing specific inhibitors that the causative signaling molecule is prostaglandin D-2 (PGD(2)) and that PGD2 call induce Sox9 transcription in Cultured XX gonads. Our data indicate a mechanism whereby Sry; uses both a cell-autonomous mechanism and a PGD(2)-mediated signaling mechanism to stimulate expression of Sox9 and induce the differentiation of Sertoli cells in vivo. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:111 / 124
页数:14
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