The Cain Foundation Laboratories, Baylor College of Medicine, Houston, Texas, United States of America.
PLoS One. 2013;8(4):e60314. doi: 10.1371/journal.pone.0060314. Epub 2013 Apr 2.
The G-protein coupled receptor 55 (GPR55) is activated by lysophosphatidylinositols and some cannabinoids. Recent studies found prominent roles for GPR55 in neuropathic/inflammatory pain, cancer and bone physiology. However, little is known about the role of GPR55 in CNS development and function. To address this question, we performed a detailed characterization of GPR55 knockout mice using molecular, anatomical, electrophysiological, and behavioral assays. Quantitative PCR studies found that GPR55 mRNA was expressed (in order of decreasing abundance) in the striatum, hippocampus, forebrain, cortex, and cerebellum. GPR55 deficiency did not affect the concentrations of endocannabinoids and related lipids or mRNA levels for several components of the endocannabinoid system in the hippocampus. Normal synaptic transmission and short-term as well as long-term synaptic plasticity were found in GPR55 knockout CA1 pyramidal neurons. Deleting GPR55 function did not affect behavioral assays assessing muscle strength, gross motor skills, sensory-motor integration, motor learning, anxiety or depressive behaviors. In addition, GPR55 null mutant mice exhibited normal contextual and auditory-cue conditioned fear learning and memory in a Pavlovian conditioned fear test. In contrast, when presented with tasks requiring more challenging motor responses, GPR55 knockout mice showed impaired movement coordination. Taken together, these results suggest that GPR55 plays a role in motor coordination, but does not strongly regulate CNS development, gross motor movement or several types of learned behavior.
G 蛋白偶联受体 55(GPR55)被溶血磷脂酰肌醇和一些大麻素激活。最近的研究发现 GPR55 在神经病理性/炎性疼痛、癌症和骨生理学中具有重要作用。然而,关于 GPR55 在中枢神经系统发育和功能中的作用知之甚少。为了解决这个问题,我们使用分子、解剖、电生理和行为测定法对 GPR55 敲除小鼠进行了详细的特征描述。定量 PCR 研究发现,GPR55 mRNA 在纹状体、海马体、前脑、皮层和小脑中表达(按丰度递减顺序排列)。GPR55 缺乏并不影响海马体中环腺苷酸系统的几个成分的内源性大麻素和相关脂质或 mRNA 水平的浓度。在 GPR55 敲除 CA1 锥体神经元中发现正常的突触传递以及短期和长期突触可塑性。删除 GPR55 功能不会影响评估肌肉力量、大运动技能、感觉运动整合、运动学习、焦虑或抑郁行为的行为测定法。此外,GPR55 缺失突变体小鼠在 Pavlovian 条件性恐惧测试中表现出正常的情境和听觉线索条件性恐惧学习和记忆。相比之下,当呈现需要更具挑战性的运动反应的任务时,GPR55 敲除小鼠表现出运动协调受损。总的来说,这些结果表明 GPR55 在运动协调中起作用,但不会强烈调节中枢神经系统发育、大运动或几种类型的习得行为。