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促性腺激素抑制而激活素诱导培养的人颗粒黄体细胞中抑制素/激活素β(B)亚基mRNA的表达。

Gonadotrophins inhibit and activin induces expression of inhibin/activin beta(B) subunit mRNA in cultured human granulosa-luteal cells.

作者信息

Liu J, Hydèn-Granskog C, Voutilainen R

机构信息

Department of Pathology, P.O.Box 21, University of Helsinki, FIN-00014 Helsinki, Finland.

出版信息

Mol Hum Reprod. 2001 Apr;7(4):319-23. doi: 10.1093/molehr/7.4.319.

Abstract

During the human menstrual cycle, serum inhibin concentrations fluctuate in a cyclic fashion. To examine the regulation of inhibin/activin beta(B) subunit gene expression in ovarian granulosa-luteal cells, the levels of beta(B) subunit mRNA were determined in primary cultures of human granulosa-luteal cells treated with gonadotrophins and protein kinase modulators. Granulosa cells were obtained from women undergoing an IVF programme. The cells were enzymatically dispersed, separated from red blood cells, and maintained in culture for 5--10 days before addition of different agents. Northern blot analysis with specific oligonucleotide probes was performed to study inhibin/activin beta(B) subunit mRNA levels. Both LH and FSH reduced the accumulation of beta(B) subunit mRNA in a dose-dependent manner. The protein kinase A activator, (Bu)(2)cAMP, and the protein kinase inhibitor staurosporine also inhibited beta(B) subunit mRNA expression dose-dependently. Activin A increased dose-dependently beta(B) subunit mRNA expression. Our study suggests that activin-induced and gonadotrophin-inhibited beta(B) subunit expression in granulosa cells might be key factors in the transition from inhibin B to inhibin A dominance during the menstrual cycle.

摘要

在人类月经周期中,血清抑制素浓度呈周期性波动。为研究卵巢颗粒黄体细胞中抑制素/激活素β(B)亚基基因表达的调控,在用促性腺激素和蛋白激酶调节剂处理的人颗粒黄体细胞原代培养物中测定了β(B)亚基mRNA的水平。颗粒细胞取自接受体外受精程序的女性。细胞经酶分散,与红细胞分离,并在添加不同试剂前培养5 - 10天。用特异性寡核苷酸探针进行Northern印迹分析以研究抑制素/激活素β(B)亚基mRNA水平。促黄体生成素(LH)和促卵泡生成素(FSH)均以剂量依赖性方式降低β(B)亚基mRNA的积累。蛋白激酶A激活剂(Bu)2cAMP和蛋白激酶抑制剂星形孢菌素也以剂量依赖性方式抑制β(B)亚基mRNA表达。激活素A剂量依赖性地增加β(B)亚基mRNA表达。我们的研究表明,激活素诱导和促性腺激素抑制颗粒细胞中β(B)亚基表达可能是月经周期中从抑制素B主导转变为抑制素A主导的关键因素。

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