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十四烷酰佛波醇乙酸酯抑制促卵泡激素诱导的大鼠卵巢颗粒细胞中胆固醇侧链裂解酶复合物的合成。

Tetradecanoyl phorbol acetate suppresses follicle-stimulating hormone-induced synthesis of the cholesterol side-chain cleavage enzyme complex in rat ovarian granulosa cells.

作者信息

Trzeciak W H, Duda T, Waterman M R, Simpson E R

机构信息

Department of Biochemistry, University of Texas Southwestern Medical School, Dallas 75235.

出版信息

J Biol Chem. 1987 Nov 5;262(31):15246-50.

PMID:2889736
Abstract

The effect of tetradecanoylphorbol acetate (TPA) on follicle-stimulating hormone (FSH)-induced synthesis of the cholesterol side-chain cleavage (SCC) enzyme complex was studied in rat ovarian granulosa cells cultured for 48 h in serum-free medium. Cell proteins were radiolabeled with [35S]methionine, followed by immunoprecipitation of cholesterol side-chain cleavage cytochrome P-450 (P-450SCC) as well as the iron-sulfur protein adrenodoxin. Polyacrylamide gel electrophoresis and fluorography of the immunoprecipitates showed that TPA, when added in combination with FSH (50 ng/ml) or dibutyryl cAMP (Bt2cAMP; 1 mM), suppressed the stimulatory effects of these compounds on the synthesis of the SCC components in a concentration-dependent fashion. The effect of TPA was accompanied by decreased progesterone formation and decreased cAMP accumulation. The structural analog of TPA, phorbol-4 alpha-didecanoate, which does not activate protein kinase C (Ca2+/phospholipid-dependent enzyme), had no effect on the FSH- or Bt2cAMP-stimulated synthesis of SCC and progesterone or on cAMP formation. In addition to inhibiting the synthesis of these proteins, TPA greatly reduced the FSH- and Bt2cAMP-induced increase in levels of mRNA encoding the precursor form of P-450SCC. It is concluded that the effect of the phorbol ester TPA to inhibit FSH-stimulated progesterone formation in cultured ovarian granulosa cells of the rat involves decreased synthesis of the components of the SCC enzyme complex due to reduced levels of mRNA encoding the precursor forms of these proteins. The results are indicative that TPA not only inhibits FSH-mediated stimulation of cAMP formation but also may block cAMP-mediated induction of SCC synthesis. It is postulated that the effects of TPA may reflect the physiological role of protein kinase C in the regulation of ovarian steroidogenesis.

摘要

在无血清培养基中培养48小时的大鼠卵巢颗粒细胞中,研究了十四酰佛波醇乙酸酯(TPA)对促卵泡激素(FSH)诱导的胆固醇侧链裂解(SCC)酶复合物合成的影响。用[35S]甲硫氨酸对细胞蛋白进行放射性标记,随后免疫沉淀胆固醇侧链裂解细胞色素P - 450(P - 450SCC)以及铁硫蛋白肾上腺皮质铁氧还蛋白。免疫沉淀物的聚丙烯酰胺凝胶电泳和荧光自显影显示,当TPA与FSH(50 ng/ml)或二丁酰环磷腺苷(Bt2cAMP;1 mM)联合添加时,以浓度依赖的方式抑制了这些化合物对SCC成分合成的刺激作用。TPA的作用伴随着孕酮生成减少和环磷腺苷积累减少。TPA的结构类似物佛波醇 - 4α - 二癸酸酯,它不激活蛋白激酶C(Ca2 + /磷脂依赖性酶),对FSH或Bt2cAMP刺激的SCC和孕酮合成或环磷腺苷形成没有影响。除了抑制这些蛋白质的合成外,TPA还大大降低了FSH和Bt2cAMP诱导的编码P - 450SCC前体形式的mRNA水平的增加。得出的结论是,佛波醇酯TPA抑制大鼠培养的卵巢颗粒细胞中FSH刺激的孕酮生成的作用涉及由于编码这些蛋白质前体形式的mRNA水平降低而导致SCC酶复合物成分的合成减少。结果表明TPA不仅抑制FSH介导的环磷腺苷形成的刺激,而且可能阻断环磷腺苷介导的SCC合成诱导。据推测,TPA的作用可能反映了蛋白激酶C在卵巢类固醇生成调节中的生理作用。

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