Department of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa.
Interdisciplinary Program in Molecular Medicine, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa.
Physiol Genomics. 2017 Nov 1;49(11):653-658. doi: 10.1152/physiolgenomics.00055.2017. Epub 2017 Sep 15.
Peroxisome proliferator-activated receptors (PPARs) are a family of conserved ligand-activated nuclear receptor transcription factors heterogeneously expressed in mammalian tissues. PPARγ is recognized as a master regulator of adipogenesis, fatty acid metabolism, and glucose homeostasis, but genetic evidence also supports the concept that PPARγ regulates the cardiovascular system, particularly vascular function and blood pressure. There is now compelling evidence that the beneficial blood pressure-lowering effects of PPARγ activation are due to its activity in vascular smooth muscle and endothelium, through its modulation of nitric oxide-dependent vasomotor function. Endothelial PPARγ regulates the production and bioavailability of nitric oxide, while PPARγ in the smooth muscle regulates the vasomotor response to nitric oxide. We recently identified retinol binding protein 7 (RBP7) as a PPARγ target gene that is specifically and selectively expressed in the endothelium. In this review, we will discuss the evidence that RBP7 is required to mediate the antioxidant effects of PPARγ and mediate PPARγ target gene selectivity in the endothelium.
过氧化物酶体增殖物激活受体 (PPARs) 是一组保守的配体激活核受体转录因子,在哺乳动物组织中异质性表达。PPARγ 被认为是脂肪生成、脂肪酸代谢和葡萄糖稳态的主要调节剂,但遗传证据也支持 PPARγ 调节心血管系统,特别是血管功能和血压的概念。现在有令人信服的证据表明,PPARγ 激活的有益降压作用是由于其在血管平滑肌和内皮中的活性,通过调节一氧化氮依赖的血管舒缩功能。内皮 PPARγ 调节一氧化氮的产生和生物利用度,而平滑肌中的 PPARγ 调节对一氧化氮的血管舒缩反应。我们最近确定视黄醇结合蛋白 7 (RBP7) 是一个 PPARγ 靶基因,它在内皮细胞中特异性和选择性表达。在这篇综述中,我们将讨论 RBP7 介导 PPARγ 的抗氧化作用和介导内皮细胞中 PPARγ 靶基因选择性所必需的证据。