| Literature DB >> 33741415 |
Tian-Liang Ma1, Yong Zhou2, Chen-Yu Zhang3, Zi-Ang Gao3, Jia-Xi Duan4.
Abstract
β-arrestin2 is a ubiquitously expressed scaffold protein localized on the cytoplasm and plasma membrane. It was originally found to bind to GPCRs, uncoupling G proteins and receptors' binding and inhibiting the signal transduction of the GPCRs. Further investigations have revealed that β-arrestin2 not only mediates the desensitization of GPCRs but also serves as a multifunctional scaffold to mediate receptor internalization, kinase activation, and regulation of various signaling pathways, such as TLR4/NF-κB, MAPK, Wnt, TGF-β, and AMPK/mTOR pathways. β-arrestin2 regulates cell invasion, migration, autophagy, angiogenesis, and anti-inflammatory effects by regulating various signaling pathways, which play a vital role in many physiological and pathological processes. This paper reviews the structure and function of β-arrestin2, the regulation of β-arrestin2 based signaling pathways. The role and mechanism of β-arrestin2 signaling have been delineated in sufficient detail. The prospect of regulating the expression and activity of β-arrestin2 in multisystem diseases holds substantial therapeutic promise.Entities:
Keywords: AMPK/mTOR; GPCR; MAPK; Signal transduction; TGF-β; TLR4/NF-κB; Wnt; β-arrestin2
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Year: 2021 PMID: 33741415 DOI: 10.1016/j.lfs.2021.119364
Source DB: PubMed Journal: Life Sci ISSN: 0024-3205 Impact factor: 5.037