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颗粒细胞抑制素生物合成的激素调节。

Hormonal regulation of granulosa cell inhibin biosynthesis.

作者信息

Bicsak T A, Tucker E M, Cappel S, Vaughan J, Rivier J, Vale W, Hsueh A J

出版信息

Endocrinology. 1986 Dec;119(6):2711-9. doi: 10.1210/endo-119-6-2711.

Abstract

The hormonal regulation of inhibin production by cultured granulosa cells from immature hypophysectomized, estrogen-treated rats was examined using a specific RIA which detects the N-terminal portion of the inhibin alpha-chain. The RIA measured bioactive inhibin of Mr about 32,000 in granulosa cell conditioned media fractionated by fast protein liquid chromatography. In the presence of 10(-7) M androstenedione, FSH stimulated inhibin production in a dose-dependent manner during a 2-day culture. Inclusion of a phosphodiesterase inhibitor decreased the EC50 for FSH from 2.6 to 0.8 ng/ml (n = 3). The stimulatory effect of FSH could be mimicked with forskolin (an adenyl cyclase activator) and with a cAMP analog, (Bu)2cAMP, consistent with FSH action mediated through a cAMP dependent pathway. Intracellular levels of inhibin were unmeasureable, suggesting that inhibin is not stored to any great extent by the granulosa cells. This finding was consistent with in vivo studies which showed that whereas FSH treatment for 2 days doubled serum inhibin levels when compared with basal levels, there was no increase in the concentration of extractable inhibin in ovarian tissue. Granulosa cells which had been exposed to 20 ng/ml FSH for 2 days to induce LH receptors produced inhibin in response to both LH and human CG during the subsequent 2-day culture, with the levels of inhibin equalling the amount inducible by FSH. In contrast, neither PRL nor terbutaline, a beta 2-adrenergic agonist, had any effect on inhibin production even though receptors for these hormones are also induced by FSH. GnRH was found to inhibit the FSH-stimulated production of inhibin (IC50, 10(-7) M), consistent with previous observations that GnRH can act at the ovarian level to inhibit granulosa cell differentiation. This inhibition by GnRH could be reversed by inclusion of a specific GnRH antagonist. On the other hand, another regulatory peptide, vasoactive intestinal peptide, slightly stimulated inhibin production. The effect of several growth factors was also tested. Insulin-like growth factor I raised not only FSH-stimulated inhibin levels, but basal levels as well. Insulin was also effective, but only at 100-fold higher concentration. Epidermal growth factor inhibited FSH-stimulated inhibin production (IC50 = 0.1 ng/ml), whereas fibroblast growth factor had no effect. Thus, granulosa cell inhibin secretion is regulated by FSH and LH but not by PRL, presumably via a cAMP-mediated pathway.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

利用一种能检测抑制素α链N端部分的特异性放射免疫分析法(RIA),研究了来自未成熟垂体切除且经雌激素处理的大鼠的培养颗粒细胞中抑制素产生的激素调节。该RIA检测了通过快速蛋白质液相色谱法分级分离的颗粒细胞条件培养基中分子量约为32,000的生物活性抑制素。在10⁻⁷ M雄烯二酮存在的情况下,促卵泡激素(FSH)在2天培养期间以剂量依赖的方式刺激抑制素的产生。加入磷酸二酯酶抑制剂可使FSH的半数有效浓度(EC50)从2.6降至0.8 ng/ml(n = 3)。FSH的刺激作用可被福斯可林(一种腺苷酸环化酶激活剂)和一种环磷酸腺苷(cAMP)类似物(二丁酰环磷腺苷,(Bu)₂cAMP)模拟,这与FSH通过cAMP依赖性途径介导的作用一致。颗粒细胞内抑制素水平无法检测到,这表明颗粒细胞不会大量储存抑制素。这一发现与体内研究结果一致,体内研究表明,与基础水平相比,FSH处理2天可使血清抑制素水平翻倍,但卵巢组织中可提取的抑制素浓度并未增加。暴露于20 ng/ml FSH 2天以诱导促黄体生成素(LH)受体的颗粒细胞,在随后的2天培养中对LH和人绒毛膜促性腺激素(hCG)均产生抑制素,其抑制素水平与FSH诱导的水平相当。相比之下,催乳素(PRL)和β₂肾上腺素能激动剂特布他林对抑制素的产生均无任何影响,尽管这些激素的受体也由FSH诱导。发现促性腺激素释放激素(GnRH)可抑制FSH刺激的抑制素产生(半数抑制浓度,IC50,10⁻⁷ M),这与之前观察到的GnRH可在卵巢水平发挥作用抑制颗粒细胞分化的结果一致。GnRH的这种抑制作用可通过加入特异性GnRH拮抗剂来逆转。另一方面,另一种调节肽,血管活性肠肽,可轻微刺激抑制素的产生。还测试了几种生长因子的作用。胰岛素样生长因子I不仅提高了FSH刺激的抑制素水平,也提高了基础水平。胰岛素也有作用,但浓度需高出100倍才行。表皮生长因子抑制FSH刺激的抑制素产生(IC50 = 0.1 ng/ml),而成纤维细胞生长因子则无作用。因此,颗粒细胞抑制素的分泌受FSH和LH调节,而不受PRL调节,推测是通过cAMP介导的途径。(摘要截短至400字)

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