Department of Pharmacology, University of Minnesota Medical School, Minneapolis, Minnesota.
Mol Pharmacol. 2013 Dec;84(6):844-53. doi: 10.1124/mol.113.088278. Epub 2013 Sep 23.
The µ-opioid receptor (OPRM1) signals as a classic G protein-coupled receptor by activating heterotrimeric Gi/Go proteins resulting in adenylyl cyclase (AC) inhibition. Such AC inhibition is desensitized after prolonged agonist treatment. However, after receptor desensitization, the intracellular cAMP level remains regulated by OPRM1, as demonstrated by the intracellular cAMP level increase or AC superactivation upon removal of an agonist or addition of an antagonist. We now demonstrate that such intracellular cAMP regulation is mediated by a novel noncanonical signaling pathway resulting from OPRM1 being converted to a receptor tyrosine kinase (RTK)-like entity. This noncanonical OPRM1 signaling is initiated by the receptor recruiting and activating Src kinase within the receptor complex, leading to phosphorylation of the OPRM1 Tyr(336) residue. Phospho-Tyr(336) serves as the docking site for growth factor receptor-bound protein/son of sevenless, leading to the recruitment and activation of the Ras/Raf-1 and subsequent phosphorylation and activation of AC5/6 by Raf-1. Such sequence of events was established by the absence of Ras/Raf1 recruitment and activation by the OPRM1-Y336F mutant, by the presence of Src kinase inhibitor 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine (PP2) or the absence of Src activity, by the presence of specific Raf-1 inhibitor GW5074 (5-iodo-3-[(3,5-dibromo-4-hydroxyphenyl) methylene]-2-indolinone) or the absence of Raf-1, or by the dominant negative RasN17 mutant. Src together with Ras activates Raf1 which was established by the inability of the Raf1-Tyr(340/341) mutant to activate AC. Hence, the phosphorylation of OPRM1 at Tyr(336) by Src serves as the trigger for the conversion of a classic Gi/Go-coupled receptor into an RTK-like entity, resulting in a noncanonical pathway even after the original Gi/Go signals are blunted.
μ-阿片受体(OPRM1)通过激活异三聚体 Gi/Go 蛋白而作为经典的 G 蛋白偶联受体信号传导,导致腺苷酸环化酶(AC)抑制。这种 AC 抑制在长期激动剂处理后会脱敏。然而,在受体脱敏后,细胞内 cAMP 水平仍然受到 OPRM1 的调节,这可以通过去除激动剂或添加拮抗剂后细胞内 cAMP 水平的增加或 AC 超激活来证明。我们现在证明,这种细胞内 cAMP 调节是由 OPRM1 转化为受体酪氨酸激酶(RTK)样实体而产生的新型非经典信号通路介导的。这种非经典的 OPRM1 信号转导是由受体在受体复合物中招募和激活Src 激酶引发的,导致 OPRM1 Tyr(336)残基磷酸化。磷酸化的 Tyr(336)作为生长因子受体结合蛋白/son of sevenless 的对接位点,导致 Ras/Raf-1 的募集和激活,随后 Raf-1 磷酸化和激活 AC5/6。通过 OPRM1-Y336F 突变体缺乏 Ras/Raf1 的募集和激活,通过 Src 激酶抑制剂 4-氨基-5-(4-氯苯基)-7-(叔丁基)吡唑并[3,4-d]嘧啶(PP2)或 Src 活性的缺乏,通过特定的 Raf-1 抑制剂 GW5074(5-碘-3-[(3,5-二溴-4-羟基苯基)亚甲基]-2-吲哚酮)或 Raf-1 的缺乏,或通过显性负 RasN17 突变体,建立了这种序列事件。Src 与 Ras 一起激活 Raf1,这可以通过 Raf1-Tyr(340/341)突变体不能激活 AC 来证明。因此,Src 对 OPRM1 Tyr(336)的磷酸化是将经典的 Gi/Go 偶联受体转化为 RTK 样实体的触发因素,即使原始的 Gi/Go 信号被阻断,也会导致非经典途径。