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Activation of the Lutropin/Choriogonadotropin Receptor Inhibits Apoptosis of Immature Leydig Cells in Primary Culture

机译:Lutropin / Choriogonadotropin受体的激活抑制未成熟Leydig细胞在原代培养中的凋亡。

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摘要

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.
机译:我们使用了表达重组人LH /绒毛膜促性腺激素(CG)受体(LHR)的未成熟大鼠Leydig细胞的增殖原代培养,以测试该受体的激活抑制凋亡的假说。我们还比较了LH / CG与表皮生长因子(EGF)和IGF-I的作用,因为以前已经证明它们可以刺激Leydig细胞增殖和/或抑制细胞凋亡。人CG(hCG),EGF和IGF-1在未成熟大鼠Leydig细胞的原代培养物中刺激ERK1 / 2和Akt的磷酸化。这三种激素还强烈刺激胸腺嘧啶核苷的掺入并抑制药物诱导的细胞凋亡。使用ERK1 / 2(UO126)或Akt磷酸化(LY294002)的选择性抑制剂,我们显示ERK1 / 2和Akt级联均参与Leydig细胞的hCG和EGF依赖性增殖,但仅涉及ERK1 / 2级联参与其抗凋亡作用。相同的策略表明,IGF-I的增殖和抗凋亡作用完全由Akt途径介导。这些结果表明,LHR的激活抑制Leydig细胞的凋亡,并且通过刺激ERK1 / 2途径抑制凋亡。

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