Ligand-gated ion channel interacting proteins and their role in neuroprotection

被引:33
作者
Li, Shupeng [1 ]
Wong, Albert H. C. [1 ]
Liu, Fang [1 ]
机构
[1] Univ Toronto, Ctr Addict & Mental Hlth, Campbell Family Mental Hlth Res Inst, Toronto, ON, Canada
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2014年 / 8卷
关键词
ligand-gated ion channels; protein-protein interaction; receptor complex; glutamate receptors; dopamine receptors; RECEPTOR-MEDIATED EXCITOTOXICITY; RANDOMIZED CONTROLLED-TRIAL; DOPAMINE D1 RECEPTOR; NMDA RECEPTOR; CALCIUM-CHANNELS; AMPA RECEPTOR; GLUTAMATE RECEPTORS; SYNAPTIC PLASTICITY; GLYCINE ANTAGONIST; ACUTE STROKE;
D O I
10.3389/fncel.2014.00125
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Ion channel receptors are a vital component of nervous system signaling, allowing rapid and direct conversion of a chemical neurotransmitter message to an electrical current. In recent decades, it has become apparent that ionotropic receptors are regulated by protein-protein interactions with other ion channels, G-protein coupled receptors and intracellular proteins. These other proteins can also be modulated by these interactions with ion channel receptors. This bidirectional functional cross-talk is important for critical cellular functions such as excitotoxicity in pathological and disease states like stroke, and for the basic dynamics of activity-dependent synaptic plasticity. Protein interactions with ion channel receptors can therefore increase the computational capacity of neuronal signaling cascades and also represent a novel target for therapeutic intervention in neuropsychiatric disease. This review will highlight some examples of ion channel receptor interactions and their potential clinical utility for neuroprotection.
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页数:5
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