PPARgamma1 and LXRalpha face a new regulator of macrophage cholesterol homeostasis and inflammatory responsiveness, AEBP1.

Amin Majdalawieh, Hyo-Sung Ro
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引用次数: 187

Abstract

Peroxisome proliferator-activated receptor gamma1 (PPARgamma1) and liver X receptor alpha (LXRalpha) are nuclear receptors that play pivotal roles in macrophage cholesterol homeostasis and inflammation; key biological processes in atherogenesis. The activation of PPARgamma1 and LXRalpha by natural or synthetic ligands results in the transactivation of ABCA1, ABCG1, and ApoE; integral players in cholesterol efflux and reverse cholesterol transport. In this review, we describe the structure, isoforms, expression pattern, and functional specificity of PPARs and LXRs. Control of PPARs and LXRs transcriptional activity by coactivators and corepressors is also highlighted. The specific roles that PPARgamma1 and LXRalpha play in inducing macrophage cholesterol efflux mediators and antagonizing macrophage inflammatory responsiveness are summarized. Finally, this review focuses on the recently reported regulatory functions that adipocyte enhancer-binding protein 1 (AEBP1) exerts on PPARgamma1 and LXRalpha transcriptional activity in the context of macrophage cholesterol homeostasis and inflammation.

Abstract Image

PPARgamma1和LXRalpha面临巨噬细胞胆固醇稳态和炎症反应的新调节因子AEBP1。
过氧化物酶体增殖物激活受体γ - 1 (PPARgamma1)和肝脏X受体α (lxrα)是核受体,在巨噬细胞胆固醇稳态和炎症中起关键作用;动脉粥样硬化发生的关键生物学过程。天然或合成配体对PPARgamma1和lxrα的激活可导致ABCA1、ABCG1和ApoE的转激活;在胆固醇外排和逆向胆固醇运输不可或缺的参与者。在这篇综述中,我们介绍了ppar和LXRs的结构、亚型、表达模式和功能特异性。还强调了辅激活因子和辅抑制因子对PPARs和LXRs转录活性的控制。本文综述了PPARgamma1和lxrα在诱导巨噬细胞胆固醇外排介质和拮抗巨噬细胞炎症反应中的具体作用。最后,本文综述了最近报道的脂肪细胞增强子结合蛋白1 (AEBP1)在巨噬细胞胆固醇稳态和炎症背景下对PPARgamma1和lxrα转录活性的调节功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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