Barak L S, Oakley R H, Laporte S A, Caron M G
Howard Hughes Medical Institute Laboratories and Departments of Cell Biology and Medicine, Duke University Medical Center, Durham, NC 27710, USA.
Proc Natl Acad Sci U S A. 2001 Jan 2;98(1):93-8. doi: 10.1073/pnas.98.1.93.
Agonist-dependent desensitization and internalization of G protein-coupled receptors (GPCR) are mediated by the binding of arrestins to phosphorylated receptors. The affinity of arrestins for the phosphorylated GPCR regulates the ability of the internalized receptor to be dephosphorylated and recycled back to the plasma membrane. In this study, we show that the naturally occurring loss of function vasopressin receptor mutation R137H, which is associated with familial nephrogenic diabetes insipidus, induces constitutive arrestin-mediated desensitization. In contrast to the wild-type vasopressin receptor, the nonsignaling R137H receptor is phosphorylated and sequestered in arrestin-associated intracellular vesicles even in the absence of agonist. Eliminating molecular determinants on the receptor that promote high affinity arrestin-receptor interaction reestablishes plasma membrane localization and the ability of the mutated receptors to signal. These findings suggest that unregulated desensitization can contribute to the etiology of a GPCR-based disease, implying that pharmacological targeting of GPCR desensitization may be therapeutically beneficial.
G蛋白偶联受体(GPCR)的激动剂依赖性脱敏和内化是由抑制蛋白与磷酸化受体的结合介导的。抑制蛋白对磷酸化GPCR的亲和力调节内化受体去磷酸化并循环回到质膜的能力。在本研究中,我们表明,与家族性肾性尿崩症相关的天然存在的功能性血管加压素受体突变R137H会诱导组成型抑制蛋白介导的脱敏。与野生型血管加压素受体相反,即使在没有激动剂的情况下,无信号传导的R137H受体也会被磷酸化并隔离在与抑制蛋白相关的细胞内小泡中。消除受体上促进高亲和力抑制蛋白-受体相互作用的分子决定因素可重新建立质膜定位以及突变受体发出信号的能力。这些发现表明,不受调控的脱敏可能导致基于GPCR的疾病的病因,这意味着对GPCR脱敏进行药理学靶向可能具有治疗益处。