Targeting ion channels for the treatment of autoimmune neuroinflammation

被引:24
作者
Bittner, Stefan [1 ]
Meuth, Sven G. [1 ]
机构
[1] Univ Munster, Dept Neurol, D-48149 Munster, Germany
关键词
channelopathy; ion channels; Kv1.3; multiple sclerosis; sodium channels; PROGRESSIVE MULTIPLE-SCLEROSIS; K(2P)5.1 POTASSIUM CHANNELS; MOUSE DENDRITIC CELLS; GATED SODIUM-CHANNEL; SPINAL-CORD-INJURY; CNS WHITE-MATTER; T-CELL; NEUROMYELITIS-OPTICA; DOUBLE-BLIND; SIGNALING MECHANISMS;
D O I
10.1177/1756285613487782
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Pharmacological targeting of ion channels has long been recognized as an attractive strategy for the treatment of various diseases. Multiple sclerosis (MS) is an autoimmune disorder of the central nervous system with a prominent neurodegenerative component. A multitude of different cell types are involved in the complex pathophysiology of this disorder, including cells of the immune system (e.g. T and B lymphocytes and microglia), the neurovascular unit (e.g. endothelial cells and astrocytes) and the central nervous system (e.g. astrocytes and neurons). The pleiotropic expression and function of ion channels gives rise to the attractive opportunity of targeting different players and pathophysiological aspects of MS by the modulation of ion channel function in a cell-type and context-specific manner. We discuss the emerging knowledge about ion channels in the context of autoimmune neuroinflammation. While some pharmacological targets are at the edge of clinical translation, others have only recently been discovered and are still under investigation. Special focus is given to those candidates that could be attractive novel targets for future therapeutic approaches in neuroimmune autoinflammation.
引用
收藏
页码:322 / 336
页数:15
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