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过氧化物酶体增殖物激活受体(PPARs)与反式抑制的分子机制

PPARs and molecular mechanisms of transrepression.

作者信息

Ricote Mercedes, Glass Christopher K

机构信息

Centro Nacional de Investigaciones Cardiovasculares (CNIC), Melchor Fernández Almagro 3, 28029 Madrid, Spain.

出版信息

Biochim Biophys Acta. 2007 Aug;1771(8):926-35. doi: 10.1016/j.bbalip.2007.02.013. Epub 2007 Mar 12.

Abstract

In the last few years, PPARs have emerged as key regulators of inflammatory and immune responses. However, the mechanistic basis of the anti-inflammatory effects of peroxisome proliferator-activated receptors (PPARs) remains poorly understood. Accumulating evidence suggests that these effects result from inhibition of signal-dependent transcription factors that mediate inflammatory programs of gene activation. Several mechanisms underlying negative regulation of gene expression by PPARs have been described. Recent studies, using siRNA, microarray analysis and macrophage-specific knockout mice, have highlighted PPARs molecular transrepression mechanism in macrophages. Identification of their mechanism of action should help promote the understanding of the physiologic roles that PPARs play in immunity and contribute to the development of new therapeutic agents.

摘要

在过去几年中,过氧化物酶体增殖物激活受体(PPARs)已成为炎症和免疫反应的关键调节因子。然而,过氧化物酶体增殖物激活受体(PPARs)抗炎作用的机制基础仍知之甚少。越来越多的证据表明,这些作用是由于抑制了介导基因激活炎症程序的信号依赖性转录因子。已经描述了PPARs对基因表达进行负调控的几种机制。最近利用小干扰RNA、微阵列分析和巨噬细胞特异性敲除小鼠进行的研究,突出了PPARs在巨噬细胞中的分子反式抑制机制。确定它们的作用机制应有助于促进对PPARs在免疫中所起生理作用的理解,并有助于开发新的治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4077/1986735/23b6f2e62729/nihms-29283-f0001.jpg

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