Spatial organization of cofilin in dendritic spines

被引:94
作者
Racz, B
Weinberg, RJ
机构
[1] Univ N Carolina, Dept Cell & Dev Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Ctr Neurosci, Chapel Hill, NC 27599 USA
关键词
cytoskeleton; anatomy; synaptic plasticity; NMDA; actin; electron microscopy;
D O I
10.1016/j.neuroscience.2005.11.025
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptic plasticity is associated with morphological changes in dendritic spines. The actin-based cytoskeleton plays a key role in regulating spine structure, and actin reorganization in spines is critical for the maintenance of long term potentiation. To test the hypothesis that a stable pool of F-actin rests in the spine "core," while a dynamic pool lies peripherally in its "shell," we performed immunoelectron microscopy in the stratum radiatum of rat hippocampus to elucidate the subcellular distribution of cofilin, an actin-depolymerizing protein that mediates reorganization of the actin cytoskeleton. We provide direct evidence that cofilin in spines avoids the core, and instead concentrates in the shell and within the postsynaptic density. These data suggest that cofilin may link synaptic plasticity to the actin remodeling that underlies changes in spine morphology. (c) 2005 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:447 / 456
页数:10
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