Bensinger Steven J, Tontonoz Peter
Howard Hughes Medical Institute, Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, 675 Charles E. Young Drive, Los Angeles, California 90049, USA.
Nature. 2008 Jul 24;454(7203):470-7. doi: 10.1038/nature07202.
The nuclear receptors known as PPARs and LXRs are lipid-activated transcription factors that have emerged as key regulators of lipid metabolism and inflammation. PPARs and LXRs are activated by non-esterified fatty acids and cholesterol metabolites, respectively, and both exert positive and negative control over the expression of a range of metabolic and inflammatory genes. The ability of these nuclear receptors to integrate metabolic and inflammatory signalling makes them attractive targets for intervention in human metabolic diseases, such as atherosclerosis and type 2 diabetes, as well as for the modulation of inflammation and immune responses.
被称为过氧化物酶体增殖物激活受体(PPARs)和肝X受体(LXRs)的核受体是脂质激活的转录因子,已成为脂质代谢和炎症的关键调节因子。PPARs和LXRs分别由非酯化脂肪酸和胆固醇代谢产物激活,二者对一系列代谢和炎症基因的表达均发挥正性和负性调控作用。这些核受体整合代谢和炎症信号的能力使其成为干预人类代谢性疾病(如动脉粥样硬化和2型糖尿病)以及调节炎症和免疫反应的有吸引力的靶点。