Synaptic Plasticity, a Symphony in GEF

被引:39
作者
Kiraly, Drew D. [1 ]
Eipper-Mains, Jodi E. [2 ]
Mains, Richard E. [1 ]
Eipper, Betty A. [1 ]
机构
[1] Univ Connecticut, Ctr Hlth, Dept Neurosci, Farmington, CT 06030 USA
[2] Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Farmington, CT 06030 USA
关键词
Actin filament; dendritic spine; post-synaptic density; RhoGTPase; Racl; RhoA; NUCLEOTIDE EXCHANGE FACTOR; DENDRITIC SPINE DEVELOPMENT; LONG-TERM POTENTIATION; RHO-FAMILY GTPASES; COLLYBISTIN-DEFICIENT MICE; PLECKSTRIN HOMOLOGY DOMAIN; RECEPTOR TYROSINE KINASES; DEVELOPING RAT-BRAIN; FRAGILE-X-SYNDROME; MENTAL-RETARDATION;
D O I
10.1021/cn100012x
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
Dendritic spines are the postsynaptic sites for the majority of excitatory synapses in the mammalian forebrain. While many spines display great stability, others change shape in a matter of seconds to minutes. These rapid alterations in dendritic spine number and size require tight control of the actin cytoskeleton, the main structural component of dendritic spines. The ability of neurons to alter spine number and size is essential for the expression of neuronal plasticity. Within spines, guanine nucleotide exchange factors (GEFs) act as critical regulators of the actin cytoskeleton by controlling the activity of Rho-GTPases. In this review, we focus on the Rho-GEFs expressed in the nucleus accumbens and localized to the postsynaptic density and, thus, positioned to effect rapid alterations in the structure of dendritic spines. We review literature that ties these GEFs to different receptor systems and intracellular signaling cascades and discuss the effects these interactions are likely to have on synaptic plasticity.
引用
收藏
页码:348 / 365
页数:18
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