Institut de la Vision, UMR S 968 INSERM, UMR 7210 CNRS, UMPC, 17 rue Moreau, 75012 Paris, France.
Prog Neurobiol. 2013 May;104:67-92. doi: 10.1016/j.pneurobio.2013.02.001. Epub 2013 Feb 27.
Chemokines - chemotactic cytokines - are small secreted proteins that attract and activate immune and non-immune cells in vitro and in vivo. It has been suggested that chemokines and their receptors play a role in the central nervous system (CNS), in addition to their well established role in the immune system. We focus here on three chemokines-CXCL12 (C-X-C motif ligand 12), CCL2 (C-C motif ligand 2), and CX3CL1 (C-X-3C motif ligand 1) - and their principal receptors - CXCR4 (C-X-C motif receptor 4), CCR2 (C-C motif receptor 2) and CX3CR1 (C-X-3C motif receptor 1), respectively. We first introduce the classification of chemokines and their G-protein coupled receptors and the main signaling pathways triggered by receptor activation. We then discuss the cellular distribution of CXCL12/CXCR4, CCL2/CCR2 and CX3CL1/CX3CR1 in adult brain and the neurotransmission and neuromodulation effects controlled by these chemokines in the adult CNS. Changes in the expression of CXCL12, CCL2 and CX3CL1 and their respective receptors are also increasingly being implicated in the pathogenesis of CNS disorders, such as Alzheimer's disease, Parkinson's disease, HIV-associated encephalopathy, stroke and multiple sclerosis, and are therefore plausible targets for future pharmacological intervention. The final section thus discusses the role of these chemokines in these pathophysiological states. In conclusion, the role of these chemokines in cellular communication may make it possible: (i) to identify new pathways of neuron-neuron, glia-glia or neuron-glia communications relevant to both normal brain function and neuroinflammatory and neurodegenerative diseases; (ii) to develop new therapeutic approaches for currently untreatable brain diseases.
趋化因子 - 趋化细胞因子 - 是小分泌蛋白,可在体外和体内吸引和激活免疫和非免疫细胞。据认为,趋化因子及其受体除了在免疫系统中的作用外,还在中枢神经系统(CNS)中发挥作用。我们在这里重点关注三种趋化因子 - CXCL12(C-X-C 基序配体 12)、CCL2(C-C 基序配体 2)和 CX3CL1(C-X-3C 基序配体 1)及其主要受体 - CXCR4(C-X-C 基序受体 4)、CCR2(C-C 基序受体 2)和 CX3CR1(C-X-3C 基序受体 1)。我们首先介绍趋化因子及其 G 蛋白偶联受体的分类,以及受体激活触发的主要信号通路。然后,我们讨论了 CXCL12/CXCR4、CCL2/CCR2 和 CX3CL1/CX3CR1 在成年大脑中的细胞分布,以及这些趋化因子在成年中枢神经系统中的神经传递和神经调节作用。CXCL12、CCL2 和 CX3CL1 及其各自受体的表达变化也越来越多地被牵连到中枢神经系统疾病的发病机制中,如阿尔茨海默病、帕金森病、HIV 相关脑病、中风和多发性硬化症,因此是未来药物干预的合理靶点。最后一节因此讨论了这些趋化因子在这些病理生理状态中的作用。总之,这些趋化因子在细胞通讯中的作用可能使我们能够:(i)确定与正常大脑功能以及神经炎症和神经退行性疾病相关的神经元-神经元、胶质细胞-胶质细胞或神经元-胶质细胞通讯的新途径;(ii)为目前无法治疗的脑部疾病开发新的治疗方法。