Department of Cell Biology, Medicine and Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
Trends Pharmacol Sci. 2012 Mar;33(3):154-64. doi: 10.1016/j.tips.2011.12.003. Epub 2012 Jan 23.
G protein-coupled receptor kinases (GRKs) regulate numerous G protein-coupled receptors (GPCRs) by phosphorylating the intracellular domain of the active receptor, resulting in receptor desensitization and internalization. GRKs also regulate GPCR trafficking in a phosphorylation-independent manner via direct protein-protein interactions. Emerging evidence suggests that GRK2, the most widely studied member of this family of kinases, modulates multiple cellular responses in various physiological contexts by either phosphorylating non-receptor substrates or interacting directly with signaling molecules. In this review, we discuss traditional and newly discovered roles of GRK2 in receptor internalization and signaling as well as its impact on non-receptor substrates. We also discuss novel exciting roles of GRK2 in the regulation of dopamine receptor signaling and in the activation and trafficking of the atypical GPCR, Smoothened (Smo).
G 蛋白偶联受体激酶(GRKs)通过磷酸化活性受体的细胞内结构域来调节众多 G 蛋白偶联受体(GPCRs),从而导致受体脱敏和内化。GRKs 还通过直接的蛋白质-蛋白质相互作用以不依赖于磷酸化的方式调节 GPCR 转运。新出现的证据表明,该激酶家族中研究最广泛的成员 GRK2 通过磷酸化非受体底物或直接与信号分子相互作用,在各种生理环境中调节多种细胞反应。在这篇综述中,我们讨论了 GRK2 在受体内化和信号转导中的传统和新发现的作用,以及它对非受体底物的影响。我们还讨论了 GRK2 在多巴胺受体信号转导以及非典型 GPCR Smoothened(Smo)的激活和转运中的新的令人兴奋的作用。