Department of Morphology and Cell Biology, Faculty of Medicine, the University of Oviedo, Oviedo, Asturias, Spain.
Instituto de Neurociencias del Principado de Asturias (INEUROPA), Asturias, Spain.
Ann N Y Acad Sci. 2020 Sep;1475(1):34-42. doi: 10.1111/nyas.14413. Epub 2020 Jun 27.
The cannabinoid CB receptor (CB R) is the most abundant G protein-coupled receptor in the central nervous system, consistent with the important role of endocannabinoids as neuromodulators. Cannabinoids also modulate the function of G protein-coupled receptor 55 (GPR55), which forms heteroreceptor complexes with the CB R in the striatum. The aim was to characterize cannabinoid CB R-GPR55 heteromers (CB R/GPR55Hets) in the basal ganglia input nuclei of nonhuman primates, Macaca fascicularis, both in projection neurons and interneurons, by the in situ proximity ligation assay. Striatal projecting neurons were identified by the retrograde neuroanatomical tracer, biotinylated dextran amine (BDA), injected into external or internal subdivisions of the globus pallidus. Triple immunofluorescent stains were carried out to visualize (1) BDA-labeled neurons, (2) CB R/GPR55Hets, and (3) striatal interneurons positive for choline acetyltransferase, parvalbumin, calretinin, or nitric oxide synthase. CB R/GPR55Hets were identified within both types of projection neurons as well as all interneurons except those that are cholinergic. Moreover, CB R/GPR55Hets were found specifically in the neuronal cell surface, and also in intracellular membranes. Further research efforts will be needed to confirm the intracellular occurrence of heteromers and their potential as therapeutic targets in diseases related to motor control imbalances, particularly within a parkinsonian context (with or without levodopa-induced dyskinesia).
大麻素 CB 受体 (CB R) 是中枢神经系统中含量最丰富的 G 蛋白偶联受体,这与其作为内源性大麻素作为神经调质的重要作用一致。大麻素还调节 G 蛋白偶联受体 55 (GPR55) 的功能,GPR55 在纹状体中与 CB R 形成异源受体复合物。本研究旨在通过原位邻近连接分析,在食蟹猴 (Macaca fascicularis) 的基底神经节输入核中,对大麻素 CB R-GPR55 异源二聚体 (CB R/GPR55Hets) 在投射神经元和中间神经元中的特征进行研究,纹状体投射神经元由逆行神经解剖示踪剂生物素化葡聚糖胺 (BDA) 注射到苍白球的外部或内部亚区来鉴定。进行三重免疫荧光染色以可视化 (1) BDA 标记的神经元,(2) CB R/GPR55Hets,以及 (3) 胆碱乙酰转移酶、parvalbumin、calretinin 或一氧化氮合酶阳性的纹状体中间神经元。CB R/GPR55Hets 不仅在两种投射神经元中被鉴定出,而且在所有中间神经元中被鉴定出,除了胆碱能神经元。此外,CB R/GPR55Hets 不仅在神经元细胞膜上被鉴定出,也在内质网膜上被鉴定出。还需要进一步的研究来证实异源二聚体的细胞内发生及其作为与运动控制失衡相关疾病的治疗靶点的潜力,特别是在帕金森病的背景下(伴有或不伴有左旋多巴诱导的运动障碍)。