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基于连接蛋白的神经胶质网络作为一种新的治疗靶点。

Connexin-Dependent Neuroglial Networking as a New Therapeutic Target.

作者信息

Charvériat Mathieu, Naus Christian C, Leybaert Luc, Sáez Juan C, Giaume Christian

机构信息

TheranexusLyon, France.

Department of Cellular and Physiological Science, Life Science Institute, University of British ColumbiaVancouver, BC, Canada.

出版信息

Front Cell Neurosci. 2017 Jun 26;11:174. doi: 10.3389/fncel.2017.00174. eCollection 2017.

Abstract

Astrocytes and neurons dynamically interact during physiological processes, and it is now widely accepted that they are both organized in plastic and tightly regulated networks. Astrocytes are connected through connexin-based gap junction channels, with brain region specificities, and those networks modulate neuronal activities, such as those involved in sleep-wake cycle, cognitive, or sensory functions. Additionally, astrocyte domains have been involved in neurogenesis and neuronal differentiation during development; they participate in the "tripartite synapse" with both pre-synaptic and post-synaptic neurons by tuning down or up neuronal activities through the control of neuronal synaptic strength. Connexin-based hemichannels are also involved in those regulations of neuronal activities, however, this feature will not be considered in the present review. Furthermore, neuronal processes, transmitting electrical signals to chemical synapses, stringently control astroglial connexin expression, and channel functions. Long-range energy trafficking toward neurons through connexin-coupled astrocytes and plasticity of those networks are hence largely dependent on neuronal activity. Such reciprocal interactions between neurons and astrocyte networks involve neurotransmitters, cytokines, endogenous lipids, and peptides released by neurons but also other brain cell types, including microglial and endothelial cells. Over the past 10 years, knowledge about neuroglial interactions has widened and now includes effects of CNS-targeting drugs such as antidepressants, antipsychotics, psychostimulants, or sedatives drugs as potential modulators of connexin function and thus astrocyte networking activity. In physiological situations, neuroglial networking is consequently resulting from a two-way interaction between astrocyte gap junction-mediated networks and those made by neurons. As both cell types are modulated by CNS drugs we postulate that neuroglial networking may emerge as new therapeutic targets in neurological and psychiatric disorders.

摘要

在生理过程中,星形胶质细胞和神经元会动态相互作用,现在人们普遍认为它们都组织在可塑性强且受到严格调控的网络中。星形胶质细胞通过基于连接蛋白的缝隙连接通道相连,具有脑区特异性,这些网络调节神经元活动,比如参与睡眠 - 觉醒周期、认知或感觉功能的活动。此外,星形胶质细胞结构域在发育过程中参与神经发生和神经元分化;它们通过控制神经元突触强度来下调或上调神经元活动,从而与突触前和突触后神经元共同参与“三联突触”。基于连接蛋白的半通道也参与这些神经元活动的调节,然而,本综述将不考虑这一特性。此外,将电信号传递到化学突触的神经元突起会严格控制星形胶质细胞连接蛋白的表达和通道功能。因此,通过连接蛋白偶联的星形胶质细胞向神经元的远程能量运输以及这些网络的可塑性在很大程度上依赖于神经元活动。神经元和星形胶质细胞网络之间的这种相互作用涉及神经元释放的神经递质、细胞因子、内源性脂质和肽,也涉及其他脑细胞类型,包括小胶质细胞和内皮细胞。在过去十年中,关于神经胶质细胞相互作用的知识不断扩展,现在包括中枢神经系统靶向药物(如抗抑郁药、抗精神病药、精神兴奋剂或镇静药物)作为连接蛋白功能潜在调节剂以及星形胶质细胞网络活动调节剂的作用。在生理情况下,神经胶质细胞网络是由星形胶质细胞缝隙连接介导的网络与神经元形成的网络之间的双向相互作用产生的。由于这两种细胞类型都受到中枢神经系统药物的调节,我们推测神经胶质细胞网络可能成为神经和精神疾病的新治疗靶点。

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