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
功能(生物学)
神经科学
计算生物学
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 & Experimental Therapeutics]
日期:2023-04-07
卷期号:75 (5): 854-884
被引量:32
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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