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催乳素可增强CCAAT增强子结合蛋白β(C/EBPβ)和过氧化物酶体增殖物激活受体γ(PPARγ)信使核糖核酸的表达,并刺激NIH-3T3细胞的成脂转化。

Prolactin enhances CCAAT enhancer-binding protein-beta (C/EBP beta) and peroxisome proliferator-activated receptor gamma (PPAR gamma) messenger RNA expression and stimulates adipogenic conversion of NIH-3T3 cells.

作者信息

Nanbu-Wakao R, Fujitani Y, Masuho Y, Muramatu M, Wakao H

机构信息

Helix Research Institute, Chiba, Japan.

出版信息

Mol Endocrinol. 2000 Feb;14(2):307-16. doi: 10.1210/mend.14.2.0420.

DOI:10.1210/mend.14.2.0420
PMID:10674402
Abstract

Extracellular stimuli trigger adipocyte differentiation by inducing the complex cascades of transcription. Transcription factors CCAAT enhancer-binding proteins (C/EBPs) and peroxisome proliferator-activated receptor gamma (PPARgamma) play crucial roles in this process. Although ectopic expression of these factors in NIH-3T3 cells, a multipotential mesenchymal stem cell line, results in adipogenic conversion, little is known as to hormonal factors that regulate adipogenesis in these cells. In this report we demonstrate that PRL, a lactogenic hormone, enhances C/EBPbeta and PPARbeta mRNA expression and augments adipogenic conversion of NIH-3T3 cells. Moreover, we show that ectopic expression of the PRL receptor in NIH-3T3 cells results in efficient adipocyte conversion when stimulated with PRL and a PPARgamma ligand, as evidenced by expression of the adipocyte differentiation-specific genes as well as the presence of fat-laden cells. We further demonstrate that signal transducer and activator of transcription 5 (Stat5), a PRL signal transducer, activates aP2 promoter in a PRL-dependent manner. These results suggest that PRL acts as an adipogenesis-enhancing hormone in NIH-3T3 cells.

摘要

细胞外刺激通过诱导复杂的转录级联反应触发脂肪细胞分化。转录因子CCAAT增强子结合蛋白(C/EBP)和过氧化物酶体增殖物激活受体γ(PPARγ)在此过程中发挥关键作用。尽管在多能间充质干细胞系NIH-3T3细胞中异位表达这些因子会导致脂肪生成转化,但对于调节这些细胞中脂肪生成的激素因子知之甚少。在本报告中,我们证明催乳素(一种泌乳激素)可增强C/EBPβ和PPARβ mRNA表达,并增强NIH-3T3细胞的脂肪生成转化。此外,我们表明,NIH-3T3细胞中催乳素受体的异位表达在受到催乳素和PPARγ配体刺激时会导致高效的脂肪细胞转化,脂肪细胞分化特异性基因的表达以及充满脂肪的细胞的存在证明了这一点。我们进一步证明,催乳素信号转导子和转录激活子5(Stat5)以催乳素依赖的方式激活aP2启动子。这些结果表明,催乳素在NIH-3T3细胞中作为一种促进脂肪生成的激素发挥作用。

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