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促性腺激素释放激素激活卵巢颗粒细胞中的磷脂酶D。在信号转导中的可能作用。

Gonadotropin-releasing hormone activates phospholipase D in ovarian granulosa cells. Possible role in signal transduction.

作者信息

Liscovitch M, Amsterdam A

机构信息

Department of Hormone Research, Weizmann Institute of Science, Rehovot, Israel.

出版信息

J Biol Chem. 1989 Jul 15;264(20):11762-7.

PMID:2663840
Abstract

We have investigated the stimulation of phospholipase D activity by the gonadotropin-releasing hormone receptor agonist [D-Ala6, des-Gly10]GnRH N-ethylamide (GnRH-A) in preovulatory, cultured granulosa cells. GnRH-A stimulated up to 10-fold accumulation of phosphatidylethanol, produced by phospholipase D phosphatidyl transferase activity when ethanol acts as the phosphatidyl group acceptor. The effect of GnRH-A was concentration dependent (EC50 = 1 nM) and was inhibited by a specific GnRH receptor antagonist. Low GnRH-A concentrations (less than 10 nM) stimulated also accumulation of phosphatidic acid, but at higher concentrations this response was attenuated. Propranolol, which inhibits phosphatidic acid phosphohydrolase, increased both basal and GnRH-A-stimulated production of phosphatidic acid. A protein kinase C activator, 12-O-tetradecanoylphorbol-13-acetate (TPA, 100 nM), increased up to 30-fold phosphatidylethanol levels. The effects of supramaximal concentrations of GnRH-A (50 nM) and TPA (1 microM) on the accumulation of phosphatidylethanol were additive, suggesting that the two agents may not act via the same mechanism. This is supported by the fact that 1-(5-isoquinolinesulfonyl)-2-methylpiperazine, a protein kinase C inhibitor, inhibited the effect of TPA 50%, but not that of GnRH-A. However, 24 h pretreatment with TPA abolished cellular response to subsequent treatment with either TPA or GnRH-A. The stimulatory action of GnRH on steroidogenesis could be mimicked by elevating endogenous phosphatidic acid levels in granulosa cells. Exogenous phospholipase D (from Streptomyces chromofuscus, 10 IU/ml) significantly increased (2.7-fold) progesterone production by the cells; under the same conditions, GnRH-A and FSH stimulated progesterone production 3- and 2.6-fold, respectively. Similarly, propranolol stimulated progesterone production 2.2-fold. These results suggest that, in granulosa cells, GnRH receptors are coupled to a phospholipase D whose activation may participate in transducing the GnRH signal for accelerated steroidogenesis. Phospholipase D activity can be independently regulated also by protein kinase C. The possible interrelationships between phospholipase D and other phospholipases which may be activated by GnRH in these ovarian cells are discussed.

摘要

我们研究了促性腺激素释放激素受体激动剂[D - Ala6,des - Gly10]GnRH N - 乙酰胺(GnRH - A)对排卵前培养的颗粒细胞中磷脂酶D活性的刺激作用。GnRH - A刺激磷脂酶D磷脂转移酶活性产生的磷脂酰乙醇积累增加高达10倍,此时乙醇作为磷脂酰基团受体。GnRH - A的作用呈浓度依赖性(EC50 = 1 nM),并被特异性GnRH受体拮抗剂抑制。低浓度的GnRH - A(小于10 nM)也刺激磷脂酸的积累,但在较高浓度时这种反应减弱。抑制磷脂酸磷酸水解酶的普萘洛尔增加了基础和GnRH - A刺激的磷脂酸产生。蛋白激酶C激活剂12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA,100 nM)使磷脂酰乙醇水平增加高达30倍。超最大浓度的GnRH - A(50 nM)和TPA(1 microM)对磷脂酰乙醇积累的作用是相加的,这表明这两种试剂可能不是通过相同的机制起作用。这一观点得到以下事实的支持:蛋白激酶C抑制剂1 - (5 - 异喹啉磺酰基)-2 - 甲基哌嗪抑制TPA的作用达50%,但不抑制GnRH - A的作用。然而,用TPA预处理24小时消除了细胞对随后用TPA或GnRH - A处理的反应。GnRH对类固醇生成的刺激作用可以通过提高颗粒细胞内源性磷脂酸水平来模拟。外源性磷脂酶D(来自产色链霉菌,10 IU/ml)显著增加了细胞的孕酮产生(2.7倍);在相同条件下,GnRH - A和促卵泡激素分别刺激孕酮产生3倍和2.6倍。同样,普萘洛尔刺激孕酮产生2.2倍。这些结果表明,在颗粒细胞中,GnRH受体与一种磷脂酶D偶联,其激活可能参与转导GnRH信号以加速类固醇生成。磷脂酶D的活性也可以由蛋白激酶C独立调节。本文讨论了磷脂酶D与这些卵巢细胞中可能被GnRH激活的其他磷脂酶之间可能的相互关系。

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