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GPR55 is a cannabinoid receptor that increases intracellular calcium and inhibits M current

机译:GPR55是一种大麻素受体可增加细胞内钙并抑制M电流

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摘要

The CB1 cannabinoid receptor mediates many of the psychoactive effects of Δ9THC, the principal active component of cannabis. However, ample evidence suggests that additional non-CB1/CB2 receptors may contribute to the behavioral, vascular, and immunological actions of Δ9THC 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 (Δ9THC, 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 Gq, G12, RhoA, actin, phospholipase C, and calcium release from IP3R-gated stores. GPR55 activation also inhibits M current. These results establish GPR55 as a cannabinoid receptor with signaling distinct from CB1 and CB2.
机译:CB1大麻素受体介导了大麻主要活性成分Δ 9 THC的许多精神活性作用。然而,大量证据表明,其他非CB1 / CB2受体可能与Δ 9 THC和内源性大麻素的行为,血管和免疫学作用有关。在这里,我们提供了GPR55(一种G蛋白偶联受体)是大麻素受体的进一步证据。 GPR55在大型背根神经节神经元中高表达,并且在被各种大麻素(Δ 9 THC,the南酰胺类似物甲酰胺和JWH015)激活后会增加这些神经元的细胞内钙。在瞬时表达GPR55的HEK293细胞中对其信号通路的检查发现,钙的增加涉及Gq,G12,RhoA,肌动蛋白,磷脂酶C和IP3R门控存储中钙的释放。 GPR55激活还抑制M电流。这些结果将GPR55建立为大麻素受体,其信号传导不同于CB1和CB2。

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