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大麻素受体2(CNR2基因)的物种差异:新型人类和啮齿动物CB2亚型的鉴定、不同组织表达以及大麻素受体配体的调节作用

Species differences in cannabinoid receptor 2 (CNR2 gene): identification of novel human and rodent CB2 isoforms, differential tissue expression and regulation by cannabinoid receptor ligands.

作者信息

Liu Q-R, Pan C-H, Hishimoto A, Li C-Y, Xi Z-X, Llorente-Berzal A, Viveros M-P, Ishiguro H, Arinami T, Onaivi E S, Uhl G R

机构信息

Mol. Neurobiol. Branch, NIDA-IRP, NIH, Baltimore, MD, USA.

出版信息

Genes Brain Behav. 2009 Jul;8(5):519-30. doi: 10.1111/j.1601-183X.2009.00498.x. Epub 2009 Jun 3.

Abstract

Cannabinoids, endocannabinoids and marijuana activate two well-characterized cannabinoid receptors (CB-Rs), CB1-Rs and CB2-Rs. The expression of CB1-Rs in the brain and periphery has been well studied, but neuronal CB2-Rs have received much less attention than CB1-Rs. Many studies have now identified and characterized functional glial and neuronal CB2-Rs in the central nervous system. However, many features of CB2-R gene structure, regulation and variation remain poorly characterized in comparison with the CB1-R. In this study, we report on the discovery of a novel human CB2 gene promoter transcribing testis (CB2A) isoform with starting exon located ca 45 kb upstream from the previously identified promoter transcribing the spleen isoform (CB2B). The 5' exons of both CB2 isoforms are untranslated 5'UTRs and alternatively spliced to the major protein coding exon of the CB2 gene. CB2A is expressed higher in testis and brain than CB2B that is expressed higher in other peripheral tissues than CB2A. Species comparison found that the CB2 gene of human, rat and mouse genomes deviated in their gene structures and isoform expression patterns. mCB2A expression was increased significantly in the cerebellum of mice treated with the CB-R mixed agonist, WIN55212-2. These results provide much improved information about CB2 gene structure and its human and rodent variants that should be considered in developing CB2-R-based therapeutic agents.

摘要

大麻素、内源性大麻素和大麻可激活两种特性明确的大麻素受体(CB-Rs),即CB1-Rs和CB2-Rs。CB1-Rs在大脑和外周的表达已得到充分研究,但神经元CB2-Rs受到的关注远少于CB1-Rs。现在许多研究已在中枢神经系统中鉴定并表征了功能性胶质细胞和神经元CB2-Rs。然而,与CB1-R相比,CB2-R基因结构、调控和变异的许多特征仍未得到充分表征。在本研究中,我们报告发现了一种新的人类CB2基因启动子,该启动子转录睾丸(CB2A)异构体,其起始外显子位于先前鉴定的转录脾脏异构体(CB2B)的启动子上游约45 kb处。两种CB2异构体的5'外显子均为非翻译5'UTR,并可选择性剪接至CB2基因的主要蛋白质编码外显子。CB2A在睾丸和大脑中的表达高于CB2B,而CB2B在其他外周组织中的表达高于CB2A。物种比较发现,人类、大鼠和小鼠基因组的CB2基因在基因结构和异构体表达模式上存在差异。在用CB-R混合激动剂WIN55212-2处理的小鼠小脑中,mCB2A表达显著增加。这些结果提供了关于CB2基因结构及其人类和啮齿动物变体的更多改进信息,在开发基于CB2-R的治疗药物时应予以考虑。

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