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Dicer 在脂肪细胞分化中起关键作用。

An essential role for Dicer in adipocyte differentiation.

机构信息

Department of Cell Biology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, Massachusetts 01655, USA.

出版信息

J Cell Biochem. 2010 Jul 1;110(4):812-6. doi: 10.1002/jcb.22625.

Abstract

Dicer is a cellular enzyme required for the processing of pre-miRNA molecules into mature miRNA, and Dicer and miRNA biogenesis have been found to play important roles in a variety of physiologic processes. Recently, reports of alterations in miRNA expression levels in cultured pre-adipogenic cell lines during differentiation and findings of differences between the miRNA expression signatures of white and brown adipose have suggested that miRNA molecules might regulate adipocyte differentiation and the formation of adipose tissue. However, direct evidence that miRNAs regulate adipogenesis is lacking. To determine if Dicer and mature miRNA govern adipocyte differentiation, we utilized primary cells isolated from mice bearing Dicer-conditional alleles to study adipogenesis in the presence or absence of miRNA biogenesis. Our results reveal that Dicer is required for adipogenic differentiation of mouse embryonic fibroblasts and primary cultures of pre-adipocytes. Furthermore, the requirement for Dicer in adipocyte differentiation is not due to miRNA-mediated alterations in cell proliferation, as deletion of the Ink4a locus and the prevention of premature cellular senescence normally induced in primary cells upon Dicer ablation fails to rescue adipogenic differentiation in fibroblasts and pre-adipocytes.

摘要

Dicer 是一种细胞内的酶,对于将 pre-miRNA 分子加工成成熟的 miRNA 是必需的,并且 Dicer 和 miRNA 的生物发生已被发现对多种生理过程起着重要作用。最近,在分化过程中培养的前脂肪细胞系中 miRNA 表达水平的变化报告,以及白色和棕色脂肪组织之间 miRNA 表达特征的差异发现,提示 miRNA 分子可能调节脂肪细胞分化和脂肪组织的形成。然而,直接证明 miRNA 调节脂肪生成的证据尚缺乏。为了确定 Dicer 和成熟 miRNA 是否控制脂肪细胞分化,我们利用携带 Dicer 条件性等位基因的小鼠分离的原代细胞,在存在或不存在 miRNA 生物发生的情况下研究脂肪生成。我们的结果表明,Dicer 对于小鼠胚胎成纤维细胞和前脂肪细胞原代培养物的脂肪生成分化是必需的。此外,Dicer 在脂肪细胞分化中的必要性不是由于 miRNA 介导的细胞增殖改变引起的,因为在 Dicer 缺失时删除 Ink4a 基因座并防止正常诱导的原代细胞过早细胞衰老,不能挽救成纤维细胞和前脂肪细胞中的脂肪生成分化。

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