Suppr超能文献

3T3-L1细胞脂肪分化过程中雌激素合成酶(P-450芳香化酶)的表达

Expression of estrogen synthetase (P-450 aromatase) during adipose differentiation of 3T3-L1 cells.

作者信息

Yamada K, Harada N

机构信息

Division of Molecular Genetics, School of Medicine, Fujita Health University, Aichi, Japan.

出版信息

Biochem Biophys Res Commun. 1990 Jun 15;169(2):531-6. doi: 10.1016/0006-291x(90)90363-r.

Abstract

The expression of estrogen synthetase (aromatase), catalyzing a rate limiting reaction in estrogen formation, was examined in 3T3-L1 cells during adipose differentiation. The expression of another P-450 enzyme, cholesterol side-chain cleavage enzyme (P-450scc) by the cells was also studied for comparison. The level of specific mRNA for aromatase increased 17-fold during adipogenic conversion and the elevated level was maintained in fully differentiated adipocytes. The level of specific mRNA for P-450scc increased about 5-fold, mainly due to net increase of cellular RNA. Various reagents, such as dexamethasone, testosterone and 1-methyl-3-isobutylxanthine, affected the expression of specific mRNA for aromatase markedly in adipocytes but had scarcely any effect on its level in fibroblasts. In contrast, these reagents caused similar increases in the level of mRNA for P-450scc in the two types of cells. Thus the 3T3-L1 cell line during adipogenic differentiation may be a useful system for studies on the mechanism regulating aromatase gene expression.

摘要

在3T3-L1细胞脂肪分化过程中,对催化雌激素形成限速反应的雌激素合成酶(芳香化酶)的表达进行了检测。为作比较,还研究了该细胞中另一种P-450酶,即胆固醇侧链裂解酶(P-450scc)的表达。在成脂转化过程中,芳香化酶特异性mRNA水平增加了17倍,且在完全分化的脂肪细胞中维持在升高水平。P-450scc特异性mRNA水平增加了约5倍,主要是由于细胞RNA的净增加。地塞米松、睾酮和1-甲基-3-异丁基黄嘌呤等多种试剂对脂肪细胞中芳香化酶特异性mRNA的表达有显著影响,但对成纤维细胞中其水平几乎没有影响。相反,这些试剂使两种细胞中P-450scc的mRNA水平有相似程度的增加。因此,3T3-L1细胞系在成脂分化过程中可能是研究芳香化酶基因表达调控机制的有用体系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验