Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, Instituto de Salud Carlos III, Madrid, Spain.
Department of Biochemistry and Molecular Biology, University of Barcelona, Barcelona, Spain.
Neuropsychopharmacology. 2018 Apr;43(5):964-977. doi: 10.1038/npp.2017.12. Epub 2017 Jan 19.
The dorsal striatum is a key node for many neurobiological processes such as motor activity, cognitive functions, and affective processes. The proper functioning of striatal neurons relies critically on metabotropic receptors. Specifically, the main adenosine and endocannabinoid receptors present in the striatum, ie, adenosine A receptor (AR) and cannabinoid CB receptor (CBR), are of pivotal importance in the control of neuronal excitability. Facilitatory and inhibitory functional interactions between striatal AR and CBR have been reported, and evidence supports that this cross-talk may rely, at least in part, on the formation of AR-CBR heteromeric complexes. However, the specific location and properties of these heteromers have remained largely unknown. Here, by using techniques that allowed a precise visualization of the heteromers in situ in combination with sophisticated genetically modified animal models, together with biochemical and pharmacological approaches, we provide a high-resolution expression map and a detailed functional characterization of AR-CBR heteromers in the dorsal striatum. Specifically, our data unveil that the AR-CBR heteromer (i) is essentially absent from corticostriatal projections and striatonigral neurons, and, instead, is largely present in striatopallidal neurons, (ii) displays a striking G protein-coupled signaling profile, where co-stimulation of both receptors leads to strongly reduced downstream signaling, and (iii) undergoes an unprecedented dysfunction in Huntington's disease, an archetypal disease that affects striatal neurons. Altogether, our findings may open a new conceptual framework to understand the role of coordinated adenosine-endocannabinoid signaling in the indirect striatal pathway, which may be relevant in motor function and neurodegenerative diseases.
背侧纹状体是许多神经生物学过程的关键节点,如运动活动、认知功能和情感过程。纹状体神经元的正常功能依赖于代谢型受体。具体来说,纹状体中存在的主要腺苷和内源性大麻素受体,即腺苷 A 受体 (AR) 和大麻素 CB 受体 (CBR),对神经元兴奋性的控制至关重要。已经报道了纹状体 AR 和 CBR 之间的促进和抑制性功能相互作用,并且有证据表明这种串扰至少部分依赖于 AR-CBR 异源三聚体的形成。然而,这些异源三聚体的特定位置和特性在很大程度上仍然未知。在这里,我们通过使用允许在原位精确可视化异源三聚体的技术,结合复杂的基因修饰动物模型以及生化和药理学方法,提供了背侧纹状体中 AR-CBR 异源三聚体的高分辨率表达图谱和详细的功能特征。具体而言,我们的数据揭示了 AR-CBR 异源三聚体 (i) 基本上不存在于皮质纹状体投射和纹状体苍白球神经元中,而是主要存在于纹状体苍白球神经元中,(ii) 显示出引人注目的 G 蛋白偶联信号转导谱,其中两个受体的共同刺激导致下游信号转导大大减少,以及 (iii) 在亨廷顿病中经历了前所未有的功能障碍,亨廷顿病是一种影响纹状体神经元的典型疾病。总的来说,我们的发现可能为理解协调的腺苷-内源性大麻素信号在间接纹状体途径中的作用提供了一个新的概念框架,这可能与运动功能和神经退行性疾病相关。