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人类卵巢基质中的I型胰岛素样生长因子受体

Type I insulin-like growth factor receptors in human ovarian stroma.

作者信息

Poretsky L, Bhargava G, Levitan E

机构信息

Department of Medicine, Beth Israel Medical Center, New York, N.Y.

出版信息

Horm Res. 1990;33(1):22-6. doi: 10.1159/000181441.

Abstract

Hyperandrogenism observed in a variety of hyperinsulinemic states is thought to be due to an effect of insulin mediated through the type I insulin-like growth factor (IGF) receptors. These receptors, however, have not yet been demonstrated in normal human ovarian cells capable of androgen production. We now report the presence of type I IGF receptors in membrane preparations of human ovarian stroma. The ovarian stromal tissue was obtained from women undergoing indicated oophorectomy. Stromal plasma membranes were prepared. Specific 125I-IGF-I binding was 6.6 +/- 0.2%/100 micrograms protein. The affinity constant estimated by Scatchard analysis was 4.6 X 10(-9) M. 50% inhibition of 125I-IGF-1 binding was observed at 5 ng/ml of IGF-1. Specificity of the 125I-IGF-I-binding sites was confirmed by analogue specificity studies and in experiments utilizing monoclonal antibody to the IGF-I receptor, alpha-IR-3. IGF-II and insulin competed with 125I-IGF-I for the binding sites, but with an affinity significantly lower than that of IGF-I: 50% inhibition was observed at approximately 60 ng/ml of IGF-II or insulin. alpha-IR-3, a monoclonal antibody with high specificity for the type I IGF receptor, effectively inhibited 125I-IGF-I binding in a dose-dependent manner, confirming that the 125I-IGF-I binding was indeed to the type I IGF receptor. We conclude that type I IGF receptors are present in human ovarian stroma. These receptors may mediate effects of insulin on the ovary in hyperinsulinemic insulin-resistant states.

摘要

在多种高胰岛素血症状态下观察到的高雄激素血症被认为是由于胰岛素通过I型胰岛素样生长因子(IGF)受体介导的作用所致。然而,这些受体尚未在能够产生雄激素的正常人类卵巢细胞中得到证实。我们现在报告在人卵巢基质的膜制剂中存在I型IGF受体。卵巢基质组织取自接受指定卵巢切除术的女性。制备了基质质膜。特异性125I-IGF-I结合量为6.6±0.2%/100微克蛋白质。通过Scatchard分析估计的亲和常数为4.6×10^(-9) M。在5 ng/ml的IGF-1时观察到125I-IGF-1结合的50%抑制。通过类似物特异性研究以及利用针对IGF-I受体的单克隆抗体α-IR-3的实验证实了125I-IGF-I结合位点的特异性。IGF-II和胰岛素与125I-IGF-I竞争结合位点,但亲和力明显低于IGF-I:在约60 ng/ml的IGF-II或胰岛素时观察到50%抑制。α-IR-3是一种对I型IGF受体具有高特异性的单克隆抗体,以剂量依赖性方式有效抑制125I-IGF-I结合,证实125I-IGF-I结合确实是与I型IGF受体结合。我们得出结论,I型IGF受体存在于人卵巢基质中。这些受体可能在高胰岛素血症胰岛素抵抗状态下介导胰岛素对卵巢的作用。

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