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Notch靶基因Hes-1在3T3-L1前脂肪细胞分化中的双重作用。

Dual roles for the Notch target gene Hes-1 in the differentiation of 3T3-L1 preadipocytes.

作者信息

Ross David A, Rao Prakash K, Kadesch Tom

机构信息

Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6145, USA.

出版信息

Mol Cell Biol. 2004 Apr;24(8):3505-13. doi: 10.1128/MCB.24.8.3505-3513.2004.

Abstract

The process of adipogenesis involves a complex program of gene expression that includes down-regulation of the gene encoding Hes-1, a target of the Notch signaling pathway. To determine if Notch signaling affects adipogenesis, we exposed 3T3-L1 preadipocytes to the Notch ligand Jagged1 and found that differentiation was significantly reduced. This effect could be mimicked by constitutive expression of Hes-1. The block was associated with a complete loss of C/EBPalpha and peroxisome proliferator-activated receptor gamma (PPARgamma) induction and could be overcome by retroviral expression of either C/EBPalpha or PPARgamma2. Surprisingly, small interfering RNA (siRNA)-mediated reduction of Hes-1 mRNA in 3T3-L1 cells also inhibited differentiation, suggesting an additional, obligatory role for Hes-1 in adipogenesis. This role may be related to our observation that both Notch signaling and Hes-1 down-regulate transcription of the gene encoding DLK/Pref-1, a protein known to inhibit differentiation of 3T3-L1 cells. The results presented in this study establish a new target downstream of the Notch-Hes-1 pathway and suggest a dual role for Hes-1 in adipocyte development.

摘要

脂肪生成过程涉及一个复杂的基因表达程序,其中包括对Notch信号通路靶点Hes-1编码基因的下调。为了确定Notch信号是否影响脂肪生成,我们将3T3-L1前脂肪细胞暴露于Notch配体Jagged1,发现分化显著降低。这种效应可通过Hes-1的组成型表达来模拟。这种阻滞与C/EBPα和过氧化物酶体增殖物激活受体γ(PPARγ)诱导的完全丧失相关,并且可以通过逆转录病毒表达C/EBPα或PPARγ2来克服。令人惊讶的是,小干扰RNA(siRNA)介导的3T3-L1细胞中Hes-1 mRNA的减少也抑制了分化,这表明Hes-1在脂肪生成中具有额外的、必不可少的作用。这个作用可能与我们的观察结果有关,即Notch信号和Hes-1都下调DLK/Pref-1编码基因的转录,DLK/Pref-1是一种已知可抑制3T3-L1细胞分化的蛋白质。本研究中的结果确立了Notch-Hes-1通路下游的一个新靶点,并提示Hes-1在脂肪细胞发育中具有双重作用。

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