Yu Lexiang, Gao Yuen, Aaron Nicole, Qiang Li
Naomi Berrie Diabetes Center, Columbia University, New York, NY, United States.
Department of Pathology and Cell Biology, Columbia University, New York, NY, United States.
Front Pharmacol. 2023 Aug 28;14:1254317. doi: 10.3389/fphar.2023.1254317. eCollection 2023.
Nuclear receptors are ligand-regulated transcription factors that regulate vast cellular activities and serve as an important class of drug targets. Among them, peroxisome proliferator-activated receptors (PPARs) are members of the nuclear receptor family and have been extensively studied for their roles in metabolism, differentiation, development, and cancer, among others. Recently, there has been considerable interest in understanding and defining the function of PPARs and their agonists in regulating innate and adaptive immune responses and their pharmacological potential in combating chronic inflammatory diseases. In this review, we focus on emerging evidence for the potential role of PPARγ in macrophage biology, which is the prior innate immune executive in metabolic and tissue homeostasis. We also discuss the role of PPARγ as a regulator of macrophage function in inflammatory diseases. Lastly, we discuss the possible application of PPARγ antagonists in metabolic pathologies.
核受体是受配体调控的转录因子,可调节广泛的细胞活动,并作为一类重要的药物靶点。其中,过氧化物酶体增殖物激活受体(PPARs)是核受体家族的成员,因其在代谢、分化、发育和癌症等方面的作用而受到广泛研究。最近,人们对理解和定义PPARs及其激动剂在调节先天性和适应性免疫反应中的功能以及它们在对抗慢性炎症性疾病中的药理潜力产生了浓厚兴趣。在这篇综述中,我们重点关注PPARγ在巨噬细胞生物学中潜在作用的新证据,巨噬细胞是代谢和组织稳态中首要的先天性免疫执行者。我们还讨论了PPARγ作为炎症性疾病中巨噬细胞功能调节剂的作用。最后,我们讨论了PPARγ拮抗剂在代谢性疾病中的可能应用。