Neurobiology Laboratory, ESPCI-ParisTech, ESPCI-CNRS UMR 7637, Paris, France.
Pharmacology. 2012;90(1-2):19-39. doi: 10.1159/000339075. Epub 2012 Jul 3.
The type-1 cannabinoid receptor (CB1R) was initially identified as the neuronal target of Δ(9)-tetrahydrocannabinol (THC), the major psychoactive substance of marijuana. This receptor is one of the most abundant G-protein-coupled receptors in the adult brain, the target of endocannabinoid ligands and a well-characterized retrograde synaptic regulator. However, CB1Rs are also highly and often transiently expressed in neuronal populations in the embryonic and early postnatal brain, even before the formation of synapses. This suggests important physiological roles for CB1Rs during neuronal development. Several recent reviews have summarized our knowledge about the role of the endocannabinoid (eCB) system in neurodevelopment and neurotransmission by focusing on the metabolism of endocannabinoid molecules. Here, we review current knowledge about the effects of the modulation of CB1R signaling during the different phases of brain development. More precisely, we focus on reports that directly implicate CB1Rs during progenitor cell migration and differentiation, neurite outgrowth, axonal pathfinding and synaptogenesis. Based on theoretical considerations and on the reviewed experimental data, we propose a new model to explain the diversity of experimental findings on eCB signaling on neurite growth and axonal pathfinding. In our model, cell-autonomus and paracrine eCBs acting on CB1Rs are part of a global inhibitory network of cytoskeletal effectors, which act in concert with positive-feedback local-excitation loops, to ultimately yield highly polarized neurons.
I 型大麻素受体 (CB1R) 最初被鉴定为 Δ(9)-四氢大麻酚 (THC) 的神经元靶点,THC 是大麻的主要精神活性物质。该受体是成人脑中最丰富的 G 蛋白偶联受体之一,是内源性大麻素配体的靶点,也是一种特征明确的逆行突触调节剂。然而,CB1R 在胚胎和出生后早期大脑的神经元群体中也高度且常常短暂表达,甚至在突触形成之前。这表明 CB1R 在神经元发育过程中具有重要的生理作用。最近的几篇综述总结了我们对内源性大麻素 (eCB) 系统在神经发育和神经传递中的作用的认识,重点关注内源性大麻素分子的代谢。在这里,我们回顾了目前关于在大脑发育的不同阶段调节 CB1R 信号对的影响的知识。更确切地说,我们专注于那些直接将 CB1R 牵连到祖细胞迁移和分化、神经突生长、轴突寻路和突触发生过程中的报告。基于理论考虑和已审查的实验数据,我们提出了一个新的模型来解释关于 eCB 信号对神经突生长和轴突寻路的实验结果的多样性。在我们的模型中,作用于 CB1R 的细胞自主和旁分泌内源性大麻素是细胞骨架效应器全局抑制网络的一部分,该网络与正反馈局部兴奋环协同作用,最终产生高度极化的神经元。