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绒毛膜促性腺激素和重组促卵泡激素对培养的人颗粒黄体细胞中抑制素α亚基和βA亚基信使核糖核酸水平的调节

Regulation of inhibin alpha- and beta A-subunit messenger ribonucleic acid levels by chorionic gonadotropin and recombinant follicle-stimulating hormone in cultured human granulosa-luteal cells.

作者信息

Erämaa M, Tuuri T, Hildén K, Ritvos O

机构信息

Department of Bacteriology and Immunology, University of Helsinki, Finland.

出版信息

J Clin Endocrinol Metab. 1994 Dec;79(6):1670-7. doi: 10.1210/jcem.79.6.7989473.

Abstract

We studied the effects of recombinant human FSH (rhFSH) and purified hCG on the steady state messenger ribonucleic acid (mRNA) levels of inhibin alpha- and beta A-subunits in cultured granulosa-luteal cells of preovulatory ovarian follicles obtained from women undergoing in vitro fertilization. Specific mRNA transcripts for the alpha- and beta A-subunits were detected in Northern and dot blot filter hybridization analyses, and the levels of these mRNAs were induced by rhFSH and hCG in a distinct concentration- and time-dependent manner. The basal and hCG-stimulated alpha-subunit mRNA levels were first determined at 2- to 3-day intervals over a 3- to 10-day culture period after the initiation of the cultures. Both the basal and hCG-stimulated alpha-subunit mRNA levels declined steadily during culture, but the maximal relative stimulatory effect of hCG was observed on day 7 of culture. All subsequent experiments, therefore, were performed on days 6-8 of culture. Both gonadotropins induced alpha-subunit mRNA levels with slower kinetics than those of the beta A-subunit. Varying between experiments, rhFSH and hCG increased the expression of the alpha-subunit with a maximal effect of 2.5- to 5.7-fold and 1.7- to 7.2-fold, respectively, above basal levels 24-48 h after stimulation. rhFSH and hCG induced beta A-subunit mRNA levels with 3.0- to 5.8-fold and 2.3- to 8.6-fold increases above basal levels, respectively, at 2 h; thereafter, only moderate or no stimulation of the beta A-subunit mRNA levels could be detected at 7-48 h. Treatment of the cells with the RNA synthesis inhibitor actinomycin-D prevented the induction of alpha-subunit mRNA levels by hCG, and no significant differences were detected in the stability of alpha-subunit mRNA transcripts in hCG-treated cells vs. untreated cultures. This indicates that hCG induces transcription of the alpha-subunit gene rather than maintains the levels of preexisting transcripts. As the kinetics of induction of alpha- and beta A-subunit mRNAs by gonadotropins were different, we examined how the inhibition of protein synthesis affects the induction of alpha- and beta A-subunit mRNAs by hCG. Cycloheximide had no effect on basal alpha-subunit mRNA levels at 2 or 24 h. However, it inhibited at 24 h the induction of the alpha-subunit by hCG.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们研究了重组人促卵泡激素(rhFSH)和纯化的人绒毛膜促性腺激素(hCG)对从接受体外受精的女性获取的排卵前卵巢卵泡的培养颗粒黄体细胞中抑制素α亚基和βA亚基的稳态信使核糖核酸(mRNA)水平的影响。在Northern印迹和斑点印迹滤膜杂交分析中检测到了α亚基和βA亚基的特异性mRNA转录本,并且这些mRNA的水平受到rhFSH和hCG以不同的浓度和时间依赖性方式诱导。在培养开始后的3至10天培养期内,每隔2至3天首先测定基础和hCG刺激的α亚基mRNA水平。在培养过程中,基础和hCG刺激的α亚基mRNA水平均稳步下降,但在培养第7天观察到hCG的最大相对刺激作用。因此,所有后续实验均在培养的第6至8天进行。两种促性腺激素诱导α亚基mRNA水平的动力学比βA亚基的慢。在不同实验中,rhFSH和hCG分别使α亚基的表达在刺激后24至48小时比基础水平最大增加2.5至5.7倍和1.7至7.2倍。rhFSH和hCG在2小时时分别使βA亚基mRNA水平比基础水平增加3.0至5.8倍和2.3至8.6倍;此后,在7至48小时仅检测到对βA亚基mRNA水平的中度刺激或无刺激。用RNA合成抑制剂放线菌素-D处理细胞可阻止hCG诱导α亚基mRNA水平,并且在hCG处理的细胞与未处理的培养物中,未检测到α亚基mRNA转录本稳定性的显著差异。这表明hCG诱导α亚基基因的转录而不是维持现有转录本的水平。由于促性腺激素诱导α亚基和βA亚基mRNA的动力学不同,我们研究了蛋白质合成的抑制如何影响hCG对α亚基和βA亚基mRNA的诱导。放线菌酮在2小时或24小时对基础α亚基mRNA水平无影响。然而,它在24小时抑制了hCG对α亚基的诱导。(摘要截短至400字)

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