Sodium channels and microglial function

被引:47
作者
Black, Joel A.
Waxman, Stephen G.
机构
[1] VA Connecticut Healthcare Syst, Rehabil Res Ctr, West Haven, CT 06516 USA
[2] Yale Univ, Dept Neurol, Sch Med, New Haven, CT 06511 USA
[3] Yale Univ, Ctr Neurosci & Regenerat Res, Sch Med, New Haven, CT 06511 USA
关键词
Cytokine; Invasion; Microglia; Migration; Phagocytosis; Sodium channel; GATED NA+ CHANNEL; HUMAN PROSTATE-CANCER; CNS WHITE-MATTER; ION CHANNELS; ENDOTHELIAL-CELLS; CALCIUM EXCHANGE; INTERFERON-GAMMA; VOLTAGE; EXPRESSION; RAT;
D O I
10.1016/j.expneurol.2011.09.030
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Microglia are resident immune cells that provide continuous surveillance within the central nervous system (CNS) and respond to perturbations of brain and spinal cord parenchyma with an array of effector functions, including proliferation, migration, phagocytosis, secretions of multiple cytokines/chemokines and promotion of repair. To sense alterations within their environment, microglia express a large number of cell surface receptors, ion channels and adhesion molecules, which activate complex and dynamic signaling pathways. In the present chapter, we review studies that demonstrate that microglia in vivo and in vitro express specific voltage-gated sodium channel isoforms, and that blockade of sodium channel activity can attenuate several effector functions of microglia. These studies also provide strong evidence that Nav1.6 is the predominant sodium channel isoform expressed in microglia and that its activity contributes to the response of microglia to multiple activating signals. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:302 / 315
页数:14
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