Literature DB >> 33741415

The role and mechanism of β-arrestin2 in signal transduction.

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.
Copyright © 2021 Elsevier Inc. All rights reserved.

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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


  1 in total

1.  β-Arrestin2-biased Drd2 agonist UNC9995 alleviates astrocyte inflammatory injury via interaction between β-arrestin2 and STAT3 in mouse model of depression.

Authors:  Yang Liu; Nanshan Song; Hang Yao; Siyuan Jiang; Yueping Wang; Ying Zheng; Yuanzhang Zhou; Jianhua Ding; Gang Hu; Ming Lu
Journal:  J Neuroinflammation       Date:  2022-10-01       Impact factor: 9.587

  1 in total

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