Department of Biochemistry, School of Medicine, Duke University, Durham, NC 27710, USA.
Medical Center, Department of Medicine, Division of Cardiology, Duke University, Durham, NC 27710, USA.
Biomolecules. 2020 Dec 23;11(1):9. doi: 10.3390/biom11010009.
The vascular endothelium is the innermost layer of blood vessels and is a key regulator of vascular tone. Endothelial function is controlled by receptor signaling through G protein-coupled receptors, receptor tyrosine kinases and receptor serine-threonine kinases. The β-arrestins, multifunctional adapter proteins, have the potential to regulate all of these receptor families, although it is unclear as to whether they serve to integrate signaling across all of these different axes. Notably, the β-arrestins have been shown to regulate signaling by a number of receptors important in endothelial function, such as chemokine receptors and receptors for vasoactive substances such as angiotensin II, endothelin-1 and prostaglandins. β-arrestin-mediated signaling pathways have been shown to play central roles in pathways that control vasodilation, cell proliferation, migration, and immune function. At this time, the physiological impact of this signaling has not been studied in detail, but a deeper understanding of it could lead to the development of novel therapies for the treatment of vascular disease.
血管内皮是血管的最内层,是血管张力的关键调节者。内皮功能受通过 G 蛋白偶联受体、受体酪氨酸激酶和受体丝氨酸-苏氨酸激酶的受体信号转导控制。多功能衔接蛋白β-arrestin 有可能调节所有这些受体家族,但尚不清楚它们是否能够整合所有这些不同轴线上的信号。值得注意的是,β-arrestin 已被证明可调节内皮功能中许多重要受体的信号,如趋化因子受体以及血管活性物质如血管紧张素 II、内皮素-1 和前列腺素的受体。β-arrestin 介导的信号通路已被证明在控制血管舒张、细胞增殖、迁移和免疫功能的途径中发挥核心作用。目前,尚未详细研究这种信号的生理影响,但更深入地了解它可能会导致开发治疗血管疾病的新疗法。