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促黄体生成素/绒毛膜促性腺激素受体的激活可抑制原代培养中未成熟睾丸间质细胞的凋亡。

Activation of the lutropin/choriogonadotropin receptor inhibits apoptosis of immature Leydig cells in primary culture.

作者信息

Tai Ping, Shiraishi Koji, Ascoli Mario

机构信息

Department of Pharmacology, Carver College of Medicine, The University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

Endocrinology. 2009 Aug;150(8):3766-73. doi: 10.1210/en.2009-0207. Epub 2009 Apr 30.

Abstract

We used proliferating primary cultures of immature rat Leydig cells expressing the recombinant human LH/choriogonadotropin (CG) receptor (LHR) to test the hypothesis that activation of this receptor inhibits apoptosis. We also compared the effects of LH/CG with epidermal growth factor (EGF) and IGF-I because these have been previously shown to stimulate proliferation and/or inhibit apoptosis in Leydig cells. Human CG (hCG), EGF, and IGF-I stimulated the phosphorylation of ERK1/2 and Akt in primary cultures of immature rat Leydig cells. These three hormones also robustly stimulated thymidine incorporation and inhibited drug-induced apoptosis. Using selective inhibitors of ERK1/2 (UO126) or Akt phosphorylation (LY294002), we show that the ERK1/2 and Akt cascades are both involved in the hCG- and EGF-dependent proliferation of Leydig cells, but only the ERK1/2 cascade is involved in their antiapoptotic actions. The same strategy showed that the proliferative and antiapoptotic actions of IGF-I are mediated entirely by the Akt pathway. These results show that activation of the LHR inhibits apoptosis in Leydig cells and that it does so through stimulation of the ERK1/2 pathway.

摘要

我们使用表达重组人促黄体生成素/绒毛膜促性腺激素(CG)受体(LHR)的未成熟大鼠睾丸间质细胞的增殖原代培养物,来验证该受体的激活可抑制细胞凋亡这一假说。我们还比较了促黄体生成素/绒毛膜促性腺激素(LH/CG)与表皮生长因子(EGF)和胰岛素样生长因子-I(IGF-I)的作用,因为先前已表明这些因子可刺激睾丸间质细胞增殖和/或抑制其凋亡。人绒毛膜促性腺激素(hCG)、EGF和IGF-I可刺激未成熟大鼠睾丸间质细胞原代培养物中ERK1/2和Akt的磷酸化。这三种激素还能强烈刺激胸腺嘧啶核苷掺入,并抑制药物诱导的细胞凋亡。使用ERK1/2的选择性抑制剂(UO126)或Akt磷酸化的选择性抑制剂(LY294002),我们发现ERK1/2和Akt信号通路均参与hCG和EGF依赖的睾丸间质细胞增殖,但只有ERK1/2信号通路参与其抗凋亡作用。同样的方法表明,IGF-I的增殖和抗凋亡作用完全由Akt信号通路介导。这些结果表明,LHR的激活可抑制睾丸间质细胞凋亡,并且是通过刺激ERK1/2信号通路来实现的。

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