Tai Ping, Shiraishi Koji, Ascoli Mario
Department of Pharmacology, Carver College of Medicine, The University of Iowa, Iowa City, Iowa 52242, USA.
Endocrinology. 2009 Aug;150(8):3766-73. doi: 10.1210/en.2009-0207. Epub 2009 Apr 30.
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.
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。