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微小RNA let-7调控3T3-L1脂肪生成。

MicroRNA let-7 regulates 3T3-L1 adipogenesis.

作者信息

Sun Tingwan, Fu Mingui, Bookout Angie L, Kliewer Steven A, Mangelsdorf David J

机构信息

Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, 75390-9050, USA.

出版信息

Mol Endocrinol. 2009 Jun;23(6):925-31. doi: 10.1210/me.2008-0298. Epub 2009 Mar 26.

Abstract

Differentiation of 3T3-L1 cells into adipocytes involves a highly orchestrated series of events including clonal expansion, growth arrest, and terminal differentiation. The mechanisms coordinating these different steps are not yet fully understood. Here we investigated whether microRNAs (miRNAs) play a role in this process. Microarray analysis was performed to detect miRNA expression during 3T3-L1 preadipocyte differentiation. Several miRNAs, including let-7, were up-regulated during 3T3-L1 adipogenesis. Ectopic introduction of let-7 into 3T3-L1 cells inhibited clonal expansion as well as terminal differentiation. The mRNA encoding high-mobility group AT-hook 2 (HMGA2), a transcription factor that regulates growth and proliferation in other contexts, was inversely correlated with let-7 levels during 3T3-L1 cell adipogenesis, and let-7 markedly reduced HMGA2 concentrations. Knockdown of HMGA2 inhibited 3T3-L1 differentiation. These results suggest that let-7 plays an important role in adipocyte differentiation and that it does so in part by targeting HMGA2, thereby regulating the transition from clonal expansion to terminal differentiation.

摘要

3T3-L1细胞向脂肪细胞的分化涉及一系列高度协调的事件,包括克隆扩增、生长停滞和终末分化。协调这些不同步骤的机制尚未完全了解。在这里,我们研究了微小RNA(miRNA)是否在这个过程中发挥作用。进行微阵列分析以检测3T3-L1前脂肪细胞分化过程中的miRNA表达。在3T3-L1脂肪生成过程中,包括let-7在内的几种miRNA上调。将let-7异位导入3T3-L1细胞可抑制克隆扩增以及终末分化。编码高迁移率族AT-钩2(HMGA2)的mRNA在3T3-L1细胞脂肪生成过程中与let-7水平呈负相关,并且let-7显著降低了HMGA2的浓度。敲低HMGA2可抑制3T3-L1分化。这些结果表明,let-7在脂肪细胞分化中起重要作用,并且部分是通过靶向HMGA2来实现的,从而调节从克隆扩增到终末分化的转变。

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