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大鼠卵巢中抗凋亡基因P11信使核糖核酸的表达:排卵前卵泡颗粒细胞中的促性腺激素刺激

Expression of messenger ribonucleic acid for the antiapoptosis gene P11 in the rat ovary: gonadotropin stimulation in granulosa cells of preovulatory follicles.

作者信息

Chun S Y, Bae H W, Kim W J, Park J H, Hsu S Y, Hsueh A J

机构信息

Hormone Research Center, Chonnam National University, Kwangju 500-757, Republic of Korea.

出版信息

Endocrinology. 2001 Jun;142(6):2311-7. doi: 10.1210/endo.142.6.8212.

Abstract

P11, a member of the S100 family of calcium-binding proteins, has been shown to interact with BAD (Bcl-xL/Bcl-2-associated death promoter) in the yeast two-hybrid protein-protein interaction assay. Because overexpression of P11 dampens the proapoptotic activity of BAD in transfected cells, we tested the possibility that the expression of this antiapoptotic protein may be regulated by gonadotropins and other survival factors in the ovary. Northern blot analysis of ovaries obtained from prepubertal rats revealed an increased expression of P11 messenger RNA (mRNA) during prepubertal development in the theca cells of preantral and early antral follicles. Treatment of immature rats with PMSG did not affect P11 expression, whereas treatment of PMSG-primed rats with an ovulatory dose of human (h)CG stimulated ovarian P11 mRNA within 6-9 h in the granulosa cells of preovulatory follicles. Treatment of cultured preovulatory follicles in vitro with LH further confirmed the time-dependent stimulation of P11 by gonadotropins. In addition, treatment of cultured preovulatory follicles with MDL-12,330A, an inhibitor of adenylate cyclase, inhibited LH-stimulated P11 mRNA, whereas treatment with forskolin, an adenylate cyclase activator, but not the protein kinase C activator, 2-O-tetradecanol-phorbal-13-acetate, mimicked the LH action, suggesting the role of adenylate cyclase activation in P11 expression. Treatment with other follicle survival factors, including the epidermal growth factor, the basic fibroblast growth factor, and interleukin-1beta, could also stimulate P11 expression in cultured preovulatory follicles. These results demonstrate the expression of P11 mRNA in theca cells of different-sized follicles and in granulosa cells of preovulatory follicles following gonadotropin stimulation, and suggest that P11 may mediate, at least partially, the survival action of gonadotropins during the ovulatory process.

摘要

P11是钙结合蛋白S100家族的成员之一,在酵母双杂交蛋白质-蛋白质相互作用试验中已显示其与BAD(Bcl-xL/Bcl-2相关死亡促进因子)相互作用。由于P11的过表达会减弱转染细胞中BAD的促凋亡活性,我们测试了这种抗凋亡蛋白的表达可能受卵巢中促性腺激素和其他存活因子调控的可能性。对青春期前大鼠卵巢进行的Northern印迹分析显示,在青春期前发育过程中,腔前卵泡和早期窦状卵泡的膜细胞中P11信使核糖核酸(mRNA)的表达增加。用孕马血清促性腺激素(PMSG)处理未成熟大鼠不会影响P11的表达,而用排卵剂量的人绒毛膜促性腺激素(hCG)处理经PMSG预处理的大鼠,可在6 - 9小时内刺激排卵前卵泡颗粒细胞中的卵巢P11 mRNA表达。用促黄体生成素(LH)体外处理培养的排卵前卵泡进一步证实了促性腺激素对P11的时间依赖性刺激作用。此外,用腺苷酸环化酶抑制剂MDL-12,330A处理培养的排卵前卵泡可抑制LH刺激的P11 mRNA表达,而用腺苷酸环化酶激活剂福斯可林处理(但不是用蛋白激酶C激活剂2-O-十四烷酰佛波醇-13-乙酸酯处理)可模拟LH的作用,这表明腺苷酸环化酶激活在P11表达中起作用。用其他卵泡存活因子处理,包括表皮生长因子、碱性成纤维细胞生长因子和白细胞介素-1β,也可刺激培养的排卵前卵泡中P11的表达。这些结果证明了在促性腺激素刺激后,不同大小卵泡的膜细胞和排卵前卵泡的颗粒细胞中P11 mRNA的表达,并表明P11可能至少部分介导了促性腺激素在排卵过程中的存活作用。

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