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RAC3 共激活因子在脂肪细胞分化中的作用。

Role of RAC3 coactivator in the adipocyte differentiation.

作者信息

Lira María Cecilia, Rosa Francisco Damian, Panelo Laura Carolina, Costas Mónica Alejandra, Rubio María Fernanda

机构信息

1Universidad de Buenos Aires, Facultad de Medicina, Instituto de Investigaciones Médicas A Lanari, Buenos Aires, Argentina.

2Consejo Nacional de Investigaciones Científicas y Técnicas, Laboratory of Molecular Biology and Apoptosis, Instituto de Investigaciones Medicas (IDIM), Universidad de Buenos Aires, Combatientes de Malvinas Av 3150, CABA, Argentina, Buenos Aires, Argentina.

出版信息

Cell Death Discov. 2018 Jul 26;4:20. doi: 10.1038/s41420-018-0085-y. eCollection 2018.

Abstract

RAC3 is a member of the p160 family of steroid receptor coactivators and it is highly expressed in several human cancers, contributing to enhanced cell proliferation and cellular transformation. In this work, we have studied the role of RAC3 in adipogenesis in L-929 cells. Adipogenesis is a highly regulated process, involving cell cycle arrest and changes in the gene expression pattern required for morphological remodelling. We found that RAC3 expression levels are downregulated during adipocyte differentiation induced by specific stimulus. In addition, cells constitutively expressing low levels of RAC3 (shRNA), showed enhanced adipocyte differentiation which was evidenced by the early detection of the adipocyte markers Perilipin, PPARγ and Oil Red O staining. Moreover, RAC3 downregulation favoured cell arrest and autophagy. Early and late autophagy inhibitors blocked adipocyte differentiation in control cells, but partially inhibited shRAC3 differentiation, demonstrating that although autophagy is required for adipogenesis, additional signals could be trigged by RAC3 downregulation. We conclude that RAC3 is a key regulator of adipogenesis, since its downregulation generates the cellular arrest and autophagic responses that are required steps for this process.

摘要

RAC3是类固醇受体共激活因子p160家族的成员,在多种人类癌症中高表达,促进细胞增殖和细胞转化。在这项研究中,我们研究了RAC3在L-929细胞脂肪生成中的作用。脂肪生成是一个高度受调控的过程,涉及细胞周期停滞以及形态重塑所需基因表达模式的变化。我们发现,在特定刺激诱导的脂肪细胞分化过程中,RAC3的表达水平下调。此外,组成性表达低水平RAC3(shRNA)的细胞显示出增强的脂肪细胞分化,这通过脂肪细胞标志物围脂滴蛋白、过氧化物酶体增殖物激活受体γ(PPARγ)的早期检测以及油红O染色得以证明。此外,RAC3的下调有利于细胞停滞和自噬。早期和晚期自噬抑制剂可阻断对照细胞中的脂肪细胞分化,但部分抑制shRAC3介导的分化,这表明尽管自噬是脂肪生成所必需的,但RAC3下调可能触发其他信号。我们得出结论,RAC3是脂肪生成的关键调节因子,因为其下调会引发细胞停滞和自噬反应,而这是该过程的必要步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/741e/6062518/3ebf4d3f0590/41420_2018_85_Fig1_HTML.jpg

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