Combinatorial morphogenesis of dendritic spines and filopodia by SPAR and α-actinin2

被引:21
作者
Hoe, Hyang-Sook [2 ]
Lee, Ji-Yun [1 ]
Pak, Daniel T. S. [1 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Pharmacol, Washington, DC 20057 USA
[2] Georgetown Univ, Med Ctr, Dept Neurosci, Washington, DC 20057 USA
关键词
Rap small GTPase; Actin cytoskeleton; Hippocampal neurons; Postsynaptic density; Structural plasticity; POSTSYNAPTIC DENSITY PROTEINS; AMPA RECEPTOR TRAFFICKING; D-ASPARTATE RECEPTORS; LONG-TERM DEPRESSION; ALPHA-ACTININ; SYNAPTIC PLASTICITY; MOLECULAR-MECHANISMS; HIPPOCAMPAL-NEURONS; NMDA RECEPTOR; KINASE-II;
D O I
10.1016/j.bbrc.2009.04.069
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rap small GTPases regulate excitatory synaptic strength and morphological plasticity of dendritic spines. Changes in spine structure are mediated by the F-actin cytoskeleton, but the link between Rap activity and actin dynamics is unclear. Here, we report a novel interaction between SPAR, a post-synaptic inhibitor of Rap, and alpha-actinin, a family of actin-cross-linking Proteins. SPAR and alpha-actinin engage in bidirectional structural plasticity of dendritic spines: SPAR promotes spine head enlargement, whereas increased alpha-actinin2 expression favors dendritic spine elongation and thinning. Surprisingly, SPAR and alpha-actinin2 can function in an additive rather than antagonistic fashion at the same dendritic spine, generating combination spine/filopodia hybrids. These data identify a molecular pathway bridging the actin cytoskeleton and Rap at synapses, and Suggest that formation of spines and filopodia are not necessarily opposing forms of structural plasticity. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 60
页数:6
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