期刊
CARDIOVASCULAR RESEARCH
卷 82, 期 2, 页码 221-228出版社
OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvp088
关键词
Sphingosine-1-phosphate; Angiogenesis; Vascular permeability; Inflammation; Retinopathy
资金
- NIH [RO1-HL49094, HL67330, HL89934]
- NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [R01HL049094, R37HL067330, R01HL067330, R01HL089934] Funding Source: NIH RePORTER
Sphingosine-1-phosphate (S1P) is now recognized as a lipid mediator that acts via G-protein-coupled receptors. S1P receptors couple to various heterotrimeric G-proteins and regulate downstream targets and ultimately cell behaviour. The prototypical S1P(1) receptor is known to couple to G(i) and regulates angiogenesis, vascular development, and immune cell trafficking. In this review, we focus our attention on the S1P(2) receptor, which has a unique G-protein-coupling property in that it preferentially activates the G(12/13) pathway. Recent studies indicate that the S1P(2) receptor regulates critical intracellular signalling pathways, such as Rho GTPase, the phosphatase PTEN, and VE-cadherin-based adherens junctions. Analysis of mutant mice has revealed the critical role of this receptor in inner ear physiology, heart and vascular development, vascular remodelling, and vascular tone, permeability, and angiogenesis in vertebrates. These studies suggest that selective modulation of S1P(2) receptor function by pharmacological tools may be useful in a variety of pathological conditions.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据