生物
G蛋白偶联受体
内化
细胞生物学
先天免疫系统
效应器
信号转导
炎症
信号转导衔接蛋白
获得性免疫系统
免疫系统
受体
免疫学
遗传学
作者
Mohammad M. Ahmadzai,David Broadbent,Christopher J. Occhiuto,Canchai Yang,Rupali Das,Hariharan Subramanian
标识
DOI:10.1016/bs.ai.2017.05.004
摘要
β-Arrestins are a highly conserved family of cytosolic adaptor proteins that contribute to many immune functions by orchestrating the desensitization and internalization of cell-surface G protein-coupled receptors (GPCRs) via well-studied canonical interactions. In cells of the innate and adaptive immune system, β-arrestins also subserve a parallel but less understood role in which they propagate, rather than terminate, intracellular signal transduction cascades. Because β-arrestins are promiscuous in their binding, they are capable of interacting with several different GPCRs and downstream effectors; in doing so, they vastly expand the repertoire of cellular responses evoked by agonist binding and the scope of responses that may contribute to inflammation during infectious and sterile insults. In this chapter, we attempt to provide an overview of the canonical and noncanonical roles of β-arrestins in inflammatory diseases.
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