期刊
CELL
卷 149, 期 5, 页码 1125-1139出版社
CELL PRESS
DOI: 10.1016/j.cell.2012.03.039
关键词
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资金
- NIH [NS044916, NS069688, HL083422, HL084583]
- Dr. Miriam and Sheldon G. Adelson Medical Research Foundation
- Eunice Kennedy Shriver National Institute of Child Health & Human Development, Baylor College of Medicine IDDRC [5P30HD024064-23]
- Mission Connect
- Grants-in-Aid for Scientific Research [23790257] Funding Source: KAKEN
AnkyrinG (ankG) is highly enriched in neurons at axon initial segments (AISs) where it clusters Na+ and K+ channels and maintains neuronal polarity. How ankG becomes concentrated at the AIS is unknown. Here, we show that as neurons break symmetry, they assemble a distal axonal submembranous cytoskeleton, comprised of ankyrinB (ankB), alpha II-spectrin, and beta II-spectrin, that defines a boundary limiting ankG to the proximal axon. Experimentally moving this boundary altered the length of ankG staining in the proximal axon, whereas disruption of the boundary through silencing of ankB, alpha II-spectrin, or beta II-spectrin expression blocked AIS assembly and permitted ankG to redistribute throughout the distal axon. In support of an essential role for the distal cytoskeleton in ankG clustering, we also found that alpha II and beta II-spectrin-deficient mice had disrupted AIS. Thus, the distal axonal cytoskeleton functions as an intra-axonal boundary restricting ankG to the AIS.
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