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Distinguished Lecture in Physiological Genomics: Experimental Biology 2016: PPARγ and retinol binding protein 7 form a regulatory hub promoting antioxidant properties of the endothelium

机译:生理基因组学杰出讲座:2016年实验生物学:PPARγ和视黄醇结合蛋白7形成促进内皮抗氧化特性的调节中心

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摘要

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.
机译:过氧化物酶体增殖物激活受体(PPAR)是在哺乳动物组织中异源表达的保守配体激活核受体转录因子家族。 PPARγ被公认为是脂肪形成,脂肪酸代谢和葡萄糖稳态的主要调节剂,但是遗传证据也支持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,通过调节一氧化氮依赖性血管舒缩功能,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。内皮中的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)作为PPARγ目标基因,在内皮细胞中特异性和选择性表达。在本文中,我们将讨论RBP7介导PPARγ的抗氧化作用和介导PPARγ靶基因在内皮中选择性的证据。

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