Waki Hironori, Yamauchi Toshimasa, Kadowaki Takashi
Department of Metabolic Diseases, Graduate School of Medicine, the University of Tokyo.
Nihon Rinsho. 2010 Feb;68(2):181-8.
PPARgamma is a member of the nuclear receptor superfamily and a molecular target of the thiazolidinedione class of antidiabetic drugs. PPARgamma was initially characterized as a central regulator of adipocyte differentiation. Recent advances in PPARgamma research have revealed diverse pathophysiological actions of PPARgamma such as regulation of expression of adipokines and inflammatory mediators, adipose tissue macrophage polarization, atherosclerosis formation and bone development. Here, we highlight recent advances in our current understanding the biological actions of PPARgamma.
过氧化物酶体增殖物激活受体γ(PPARγ)是核受体超家族的成员,也是噻唑烷二酮类抗糖尿病药物的分子靶点。PPARγ最初被表征为脂肪细胞分化的核心调节因子。PPARγ研究的最新进展揭示了PPARγ的多种病理生理作用,如调节脂肪因子和炎症介质的表达、脂肪组织巨噬细胞极化、动脉粥样硬化形成和骨骼发育。在此,我们重点介绍目前对PPARγ生物学作用理解的最新进展。