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过氧化物酶体增殖物激活受体γ 和 RhoBTB1 与高血压。

PPARγ and RhoBTB1 in hypertension.

机构信息

Department of Pharmacology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa Department of Physiology, Cardiovascular Center, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

出版信息

Curr Opin Nephrol Hypertens. 2020 Mar;29(2):161-170. doi: 10.1097/MNH.0000000000000579.

Abstract

PURPOSE OF REVIEW

This review provides an up-to-date understanding of how peroxisome proliferator activated receptor γ (PPARγ) exerts its cardioprotective effect in the vasculature through its activation of novel PPARγ target genes in endothelium and vascular smooth muscle.

RECENT FINDINGS

In vascular endothelial cells, PPARγ plays a protective role by increasing nitric oxide bioavailability and preventing oxidative stress. RBP7 is a PPARγ target gene enriched in vascular endothelial cells, which is likely to form a positive feedback loop with PPARγ. In vascular smooth muscle cells, PPARγ antagonizes the renin-angiotensin system, maintains vascular integrity, suppresses vasoconstriction, and promotes vasodilation through distinct pathways. Rho-related BTB domain containing protein 1 (RhoBTB1) is a novel PPARγ gene target in vascular smooth muscle cells that mediates the protective effect of PPARγ by serving as a substrate adaptor between the Cullin-3 RING ubiquitin ligase and phosphodiesterase 5, thus restraining its activity through ubiquitination and proteasomal degradation.

SUMMARY

In the vasculature, PPARγ exerts its cardioprotective effect through its transcriptional activity in endothelium and vascular smooth muscle. From the understanding of PPARγ's transcription targets in those pathways, novel hypertension therapy target(s) will emerge.

摘要

目的综述

本综述介绍了过氧化物酶体增殖物激活受体 γ(PPARγ)通过其在内皮细胞和血管平滑肌中激活新型 PPARγ 靶基因,从而发挥其在血管中的心脏保护作用。

最新发现

在内皮细胞中,PPARγ 通过增加一氧化氮生物利用度和防止氧化应激发挥保护作用。RBP7 是富含在内皮细胞中的 PPARγ 靶基因,可能与 PPARγ 形成正反馈回路。在血管平滑肌细胞中,PPARγ 通过不同途径拮抗肾素-血管紧张素系统,维持血管完整性,抑制血管收缩,促进血管舒张。Rho 相关 BTB 结构域蛋白 1(RhoBTB1)是血管平滑肌细胞中新型的 PPARγ 基因靶标,通过作为 Cullin-3 RING 泛素连接酶和磷酸二酯酶 5 之间的衔接物,介导 PPARγ 的保护作用,从而通过泛素化和蛋白酶体降解来抑制其活性。

总结

在血管中,PPARγ 通过其在内皮细胞和血管平滑肌中的转录活性发挥其心脏保护作用。从这些途径中了解 PPARγ 的转录靶标,将会出现新的高血压治疗靶点。

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