β−Arrestins: Structure, Function, Physiology, and Pharmacological Perspectives

G蛋白偶联受体 逮捕 生物 细胞生物学 效应器 信号转导 细胞内 神经科学
作者
Jürgen Wess,Antwi‐Boasiako Oteng,Osvaldo Rivera‐Gonzalez,Eugenia V. Gurevich,Vsevolod V. Gurevich
出处
期刊:Pharmacological Reviews [American Society for Pharmacology and Experimental Therapeutics]
卷期号:75 (5): 854-884 被引量:102
标识
DOI:10.1124/pharmrev.121.000302
摘要

The two beta-arrestins, beta-arrestin-1 and -2 (systematic names: arrestin-2 and -3, respectively), are multifunctional intracellular proteins that regulate the activity of a very large number of cellular signaling pathways and physiological functions. The two proteins were discovered for their ability to disrupt signaling via G protein-coupled receptors (GPCRs) via binding to the activated receptors. However, it is now well recognized that both beta-arrestins can also act as direct modulators of numerous cellular processes via either GPCR-dependent or -independent mechanisms. Recent structural, biophysical, and biochemical studies have provided novel insights into how beta-arrestins bind to activated GPCRs and downstream effector proteins. Studies with beta-arrestin mutant mice have identified numerous physiological and pathophysiological processes regulated by beta-arrestin-1 and/or -2. Following a brief summary of recent structural studies, this review will primarily focus on beta-arrestin-regulated physiological functions, with particular focus on the central nervous system and the roles of beta-arrestins in carcinogenesis and key metabolic processes including the maintenance of glucose and energy homeostasis. This review will also highlight potential therapeutic implications of these studies and discuss strategies that could prove useful for targeting specific beta-arrestin-regulated signaling pathways for therapeutic purposes. Significance Statement The two beta-arrestins, structurally closely related intracellular proteins that are evolutionarily highly conserved, have emerged as multifunctional proteins able to regulate a vast array of cellular and physiological functions. The outcome of studies with beta-arrestin mutant mice and cultured cells, complemented by novel insights into beta-arrestin structure and function, should pave the way for the development of novel classes of therapeutically useful drugs capable of regulating specific beta-arrestin functions.
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