Lauckner Jane E, Jensen Jill B, Chen Huei-Ying, Lu Hui-Chen, Hille Bertil, Mackie Ken
Departments of Physiology and Biophysics, University of Washington, Seattle, WA 98195, USA.
Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2699-704. doi: 10.1073/pnas.0711278105. Epub 2008 Feb 8.
The CB(1) cannabinoid receptor mediates many of the psychoactive effects of Delta(9)THC, the principal active component of cannabis. However, ample evidence suggests that additional non-CB(1)/CB(2) receptors may contribute to the behavioral, vascular, and immunological actions of Delta(9)THC and endogenous cannabinoids. Here, we provide further evidence that GPR55, a G protein-coupled receptor, is a cannabinoid receptor. GPR55 is highly expressed in large dorsal root ganglion neurons and, upon activation by various cannabinoids (Delta(9)THC, the anandamide analog methanandamide, and JWH015) increases intracellular calcium in these neurons. Examination of its signaling pathway in HEK293 cells transiently expressing GPR55 found the calcium increase to involve G(q), G(12), RhoA, actin, phospholipase C, and calcium release from IP(3)R-gated stores. GPR55 activation also inhibits M current. These results establish GPR55 as a cannabinoid receptor with signaling distinct from CB(1) and CB(2).
CB(1)大麻素受体介导了大麻主要活性成分Δ(9)四氢大麻酚(Delta(9)THC)的许多精神活性作用。然而,大量证据表明,其他非CB(1)/CB(2)受体可能也参与了Δ(9)THC和内源性大麻素的行为、血管及免疫作用。在此,我们提供进一步证据表明,G蛋白偶联受体GPR55是一种大麻素受体。GPR55在大型背根神经节神经元中高度表达,并且在被多种大麻素(Δ(9)THC、花生四烯酸乙醇胺类似物甲基花生四烯酸乙醇胺和JWH015)激活后,会使这些神经元内的细胞内钙增加。对瞬时表达GPR55的HEK293细胞中的信号通路进行研究发现,钙增加涉及G(q)、G(12)、RhoA、肌动蛋白、磷脂酶C以及从IP(3)R门控储存库释放钙。GPR55的激活还会抑制M电流。这些结果确立了GPR55作为一种信号传导不同于CB(1)和CB(2)的大麻素受体。