Yamada K, Harada N
Division of Molecular Genetics, School of Medicine, Fujita Health University, Aichi, Japan.
Biochem Biophys Res Commun. 1990 Jun 15;169(2):531-6. doi: 10.1016/0006-291x(90)90363-r.
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.
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。