Functional implications of axon initial segment cytoskeletal disruption in stroke

被引:12
作者
Stoler, Ohad [1 ]
Fleidervish, Ilya A. [1 ]
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Physiol & Cell Biol, IL-84105 Beer Sheva, Israel
关键词
axon initial segment; stroke; Ca2+; calpain; spreading depression; sodium channels; ACTION-POTENTIAL INITIATION; GATED SODIUM-CHANNELS; ACTIVITY-DEPENDENT RELOCATION; ANKYRIN-G; ION CHANNELS; SPREADING DEPRESSION; PANNEXIN CHANNELS; P2X(7) RECEPTORS; NEURONAL DEATH; CALCIUM-ENTRY;
D O I
10.1038/aps.2015.107
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Axon initial segment (AIS) is the proximal part of the axon, which is not covered with a myelin sheath and possesses a distinctive, specialized assembly of voltage-gated ion channels and associated proteins. AIS plays critical roles in synaptic integration and action potential generation in central neurons. Recent evidence shows that stroke causes rapid, irreversible calpain-mediated proteolysis of the AIS cytoskeleton of neurons surrounding the ischemic necrotic core. A better understanding of the molecular mechanisms underlying this "non-lethal" neuronal damage might provide new therapeutic strategies for improving stroke outcome. Here, we present a brief overview of the structure and function of the AIS. We then discuss possible mechanisms underlying stroke-induced AIS damage, including the roles of calpains and possible sources of Ca2+ ions, which are necessary for the activation of calpains. Finally, we discuss the potential functional implications of the loss of the AIS cytoskeleton and ion channel clusters for neuronal excitability.
引用
收藏
页码:75 / 81
页数:7
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