Ryberg E, Larsson N, Sjögren S, Hjorth S, Hermansson N-O, Leonova J, Elebring T, Nilsson K, Drmota T, Greasley P J
Department of Lead Generation, AstraZeneca R&D, Mölndal, Sweden.
Br J Pharmacol. 2007 Dec;152(7):1092-101. doi: 10.1038/sj.bjp.0707460. Epub 2007 Sep 17.
The endocannabinoid system functions through two well characterized receptor systems, the CB1 and CB2 receptors. Work by a number of groups in recent years has provided evidence that the system is more complicated and additional receptor types should exist to explain ligand activity in a number of physiological processes.
Cells transfected with the human cDNA for GPR55 were tested for their ability to bind and to mediate GTPgammaS binding by cannabinoid ligands. Using an antibody and peptide blocking approach, the nature of the G-protein coupling was determined and further demonstrated by measuring activity of downstream signalling pathways.
We demonstrate that GPR55 binds to and is activated by the cannabinoid ligand CP55940. In addition endocannabinoids including anandamide and virodhamine activate GTPgammaS binding via GPR55 with nM potencies. Ligands such as cannabidiol and abnormal cannabidiol which exhibit no CB1 or CB2 activity and are believed to function at a novel cannabinoid receptor, also showed activity at GPR55. GPR55 couples to Galpha13 and can mediate activation of rhoA, cdc42 and rac1.
These data suggest that GPR55 is a novel cannabinoid receptor, and its ligand profile with respect to CB1 and CB2 described here will permit delineation of its physiological function(s).
内源性大麻素系统通过两个特征明确的受体系统发挥作用,即CB1和CB2受体。近年来多个研究小组的工作提供了证据,表明该系统更为复杂,应该存在其他受体类型来解释许多生理过程中的配体活性。
对转染了人GPR55 cDNA的细胞进行检测,以确定其结合大麻素配体并介导GTPγS结合的能力。使用抗体和肽阻断方法,确定G蛋白偶联的性质,并通过测量下游信号通路的活性进一步证实。
我们证明GPR55与大麻素配体CP55940结合并被其激活。此外,包括花生四烯酸乙醇胺和维罗胺在内的内源性大麻素以纳摩尔效力通过GPR55激活GTPγS结合。诸如大麻二酚和异常大麻二酚等不表现出CB1或CB2活性且被认为在新型大麻素受体上起作用的配体,在GPR55上也显示出活性。GPR55与Gα13偶联,并可介导rhoA、cdc42和rac1的激活。
这些数据表明GPR55是一种新型大麻素受体,此处描述的其相对于CB1和CB2的配体谱将有助于阐明其生理功能。