Abstract
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 Ca 2+ 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.
| Original language | American English |
|---|---|
| Pages (from-to) | 75-81 |
| Number of pages | 7 |
| Journal | Acta Pharmacologica Sinica |
| Volume | 37 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Jan 2016 |
Keywords
- Ca2+
- axon initial segment
- calpain
- sodium channels
- spreading depression
- stroke
All Science Journal Classification (ASJC) codes
- Pharmacology (medical)
- Pharmacology