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生长因子对培养猪卵泡膜细胞类固醇生成的调节作用

Regulation of steroidogenesis in cultured porcine theca cells by growth factors.

作者信息

Caubo B, DeVinna R S, Tonetta S A

机构信息

Department of Obstetrics and Gynecology, University of Southern California, School of Medicine, Los Angeles 90033.

出版信息

Endocrinology. 1989 Jul;125(1):321-6. doi: 10.1210/endo-125-1-321.

Abstract

Growth factors [insulin-like growth factors (IGF-I, IGF-II), transforming growth factor-beta (TGF beta), epidermal growth factors (EGF)], found in the ovary and known to alter granulosal function, were assessed for their ability to modulate porcine thecal steroidogenesis. Theca cells from large porcine follicles (8-10 mm) were plated (5 x 10(5) cells/ml.well) in serum-free M199, treated with increasing doses of growth factors: IGF-1 (0.1-50 ng/ml), IGF-II (0.5-200 ng/ml), EGF (0.021-100 ng/ml), TGF beta (0.001-40 ng/ml), or insulin (0.01-50 micrograms/ml), with or without human CG [(hCG); 20 ng/ml], and incubated for 72 h. Levels of steroids in media were determined by RIA. Insulin increased (P less than 0.05) basal and gonadotropin-induced secretion of androstenedione, progesterone, estradiol, and testosterone. IGF-I increased (P less than 0.05) the basal and hCG-induced secretion of progesterone and androstenedione at the highest doses, but did not affect basal secretion of estradiol or testosterone. IGF-II, at the highest doses, increased (P less than 0.05) thecal steroidogenesis, but only after administration of hCG. In contrast, TGF beta increased (P less than 0.05) basal and gonadotrophin-induced secretion of estradiol but inhibited thecal secretion of progesterone, androstenedione, and testosterone. EGF did not alter thecal secretion of progesterone, androstenedione, or testosterone but significantly (P less than 0.05) inhibited basal and hCG-stimulated secretion of estradiol. In conclusion, insulin IGF-I, IGF-II, EGF, and TGF beta can modulate steroidogenesis in porcine theca cells.

摘要

在卵巢中发现的、已知可改变颗粒细胞功能的生长因子[胰岛素样生长因子(IGF-I、IGF-II)、转化生长因子-β(TGFβ)、表皮生长因子(EGF)],对其调节猪卵泡膜细胞类固醇生成的能力进行了评估。将来自大型猪卵泡(8 - 10毫米)的卵泡膜细胞以(5×10⁵个细胞/毫升·孔)接种于无血清的M199中,用递增剂量的生长因子进行处理:IGF-1(0.1 - 50纳克/毫升)、IGF-II(0.5 - 200纳克/毫升)、EGF(0.021 - 100纳克/毫升)、TGFβ(0.001 - 40纳克/毫升)或胰岛素(0.01 - 50微克/毫升),添加或不添加人绒毛膜促性腺激素[(hCG);20纳克/毫升],并孵育72小时。通过放射免疫分析法测定培养基中类固醇的水平。胰岛素增加了(P < 0.05)基础状态下以及促性腺激素诱导的雄烯二酮、孕酮、雌二醇和睾酮的分泌。IGF-I在最高剂量时增加了(P < 0.05)基础状态下以及hCG诱导的孕酮和雄烯二酮的分泌,但不影响基础状态下雌二醇或睾酮的分泌。IGF-II在最高剂量时增加了(P < 0.05)卵泡膜细胞类固醇生成,但仅在给予hCG后。相比之下,TGFβ增加了(P < 0.05)基础状态下以及促性腺激素诱导的雌二醇分泌,但抑制了卵泡膜细胞孕酮、雄烯二酮和睾酮的分泌。EGF未改变卵泡膜细胞孕酮、雄烯二酮或睾酮的分泌,但显著(P < 0.05)抑制了基础状态下以及hCG刺激的雌二醇分泌。总之,胰岛素、IGF-I、IGF-II、EGF和TGFβ可调节猪卵泡膜细胞的类固醇生成。

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