Department of Pharmacology and Physiology, University of Rochester Medical Center Rochester, NY, USA.
Front Neurosci. 2012 Dec 13;6:180. doi: 10.3389/fnins.2012.00180. eCollection 2012.
The pituitary receptor for thyrotropin-releasing hormone (TRH) is a calcium-mobilizing G protein-coupled receptor (GPCR) that signals through Gq/11, elevating calcium, and activating protein kinase C. TRH receptor signaling is quickly desensitized as a consequence of receptor phosphorylation, arrestin binding, and internalization. Following activation, TRH receptors are phosphorylated at multiple Ser/Thr residues in the cytoplasmic tail. Phosphorylation catalyzed by GPCR kinase 2 (GRK2) takes place rapidly, reaching a maximum within seconds. Arrestins bind to two phosphorylated regions, but only arrestin bound to the proximal region causes desensitization and internalization. Phosphorylation at Thr365 is critical for these responses. TRH receptors internalize in clathrin-coated vesicles with bound arrestin. Following endocytosis, vesicles containing phosphorylated TRH receptors soon merge with rab5-positive vesicles. Over approximately 20 min these form larger endosomes rich in rab4 and rab5, early sorting endosomes. After TRH is removed from the medium, dephosphorylated receptors start to accumulate in rab4-positive, rab5-negative recycling endosomes. The mechanisms responsible for sorting dephosphorylated receptors to recycling endosomes are unknown. TRH receptors from internal pools help repopulate the plasma membrane. Dephosphorylation of TRH receptors begins when TRH is removed from the medium regardless of receptor localization, although dephosphorylation is fastest when the receptor is on the plasma membrane. Protein phosphatase 1 is involved in dephosphorylation but the details of how the enzyme is targeted to the receptor remain obscure. It is likely that future studies will identify biased ligands for the TRH receptor, novel arrestin-dependent signaling pathways, mechanisms responsible for targeting kinases and phosphatases to the receptor, and principles governing receptor trafficking.
促甲状腺激素释放激素(TRH)的垂体受体是一种钙动员 G 蛋白偶联受体(GPCR),通过 Gq/11 信号转导,升高钙并激活蛋白激酶 C。TRH 受体信号转导很快被受体磷酸化、衔接蛋白结合和内化所脱敏。受体激活后,在胞质尾部的多个丝氨酸/苏氨酸残基上发生磷酸化。G 蛋白偶联受体激酶 2(GRK2)催化的磷酸化迅速发生,在几秒钟内达到最大值。衔接蛋白结合到两个磷酸化区域,但只有结合到近端区域的衔接蛋白引起脱敏和内化。Thr365 的磷酸化对于这些反应至关重要。TRH 受体与结合的衔接蛋白一起在网格蛋白包被的小泡中内化。内吞作用后,含有磷酸化 TRH 受体的小泡很快与 rab5 阳性小泡融合。大约 20 分钟后,这些小泡形成富含 rab4 和 rab5 的较大内体,即早期分拣内体。TRH 从培养基中去除后,去磷酸化的受体开始在 rab4 阳性、rab5 阴性的再循环内体中积累。负责将去磷酸化受体分拣到再循环内体的机制尚不清楚。来自内部池的 TRH 受体有助于重新填充质膜。无论受体定位如何,只要从中去除 TRH,TRH 受体就开始去磷酸化,但当受体位于质膜上时,去磷酸化速度最快。蛋白磷酸酶 1 参与去磷酸化,但酶靶向受体的细节仍不清楚。未来的研究很可能会鉴定出 TRH 受体的偏向配体、新型衔接蛋白依赖性信号通路、负责将激酶和磷酸酶靶向受体的机制以及调节受体运输的原则。