Inflammation Chemokines and Immunopathology, INSERM, UMR 996, Faculté de Médecine, Université Paris-Sud, Université Paris-Saclay, 92140 Clamart, France.
Cells. 2021 Jan 5;10(1):75. doi: 10.3390/cells10010075.
Although G protein-coupled receptor kinases (GRKs) have long been known to regulate G protein-coupled receptor (GPCR) desensitization, their more recently characterized functions as scaffolds and signalling adapters underscore that this small family of proteins governs a larger array of physiological functions than originally suspected. This review explores how GRKs contribute to the complex signalling networks involved in the migration of immune cells along chemokine gradients sensed by cell surface GPCRs. We outline emerging evidence indicating that the coordinated docking of several GRKs on an active chemokine receptor determines a specific receptor phosphorylation barcode that will translate into distinct signalling and migration outcomes. The guidance cues for neutrophil migration are emphasized based on several alterations affecting GRKs or GPCRs reported to be involved in pathological conditions.
尽管 G 蛋白偶联受体激酶(GRKs)长期以来一直被认为可以调节 G 蛋白偶联受体(GPCR)脱敏,但它们最近被描述为支架和信号适配器的功能强调了这个小蛋白家族调节的生理功能比最初预期的要多。本综述探讨了 GRKs 如何参与涉及免疫细胞沿着细胞表面 GPCR 感知的趋化因子梯度迁移的复杂信号网络。我们概述了新出现的证据,表明几种 GRKs 在活跃的趋化因子受体上的协调对接决定了特定的受体磷酸化条码,这将转化为不同的信号转导和迁移结果。强调了基于几种报道涉及病理条件的影响 GRKs 或 GPCR 的改变对中性粒细胞迁移的导向线索。