Neuronal cytoskeleton in synaptic plasticity and regeneration

被引:81
作者
Gordon-Weeks, Phillip R. [1 ]
Fournier, Alyson E. [2 ]
机构
[1] Kings Coll London, MRC Ctr Dev Neurobiol, London WC2R 2LS, England
[2] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
基金
加拿大健康研究院;
关键词
actin; axon regeneration; cytoskeleton; microtubule; neuronal plasticity; OLIGODENDROCYTE-MYELIN GLYCOPROTEIN; DENDRITIC SPINE MORPHOLOGY; END-BINDING-PROTEIN; GROWTH-CONE; AXON REGENERATION; MICROTUBULE GROWTH; F-ACTIN; FUNCTIONAL RECOVERY; RHO; CORD;
D O I
10.1111/jnc.12502
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
During development, dynamic changes in the axonal growth cone and dendrite are necessary for exploratory movements underlying initial axo-dendritic contact and ultimately the formation of a functional synapse. In the adult central nervous system, an impressive degree of plasticity is retained through morphological and molecular rearrangements in the pre- and post-synaptic compartments that underlie the strengthening or weakening of synaptic pathways. Plasticity is regulated by the interplay of permissive and inhibitory extracellular cues, which signal through receptors at the synapse to regulate the closure of critical periods of developmental plasticity as well as by acute changes in plasticity in response to experience and activity in the adult. The molecular underpinnings of synaptic plasticity are actively studied and it is clear that the cytoskeleton is a key substrate for many cues that affect plasticity. Many of the cues that restrict synaptic plasticity exhibit residual activity in the injured adult CNS and restrict regenerative growth by targeting the cytoskeleton. Here, we review some of the latest insights into how cytoskeletal remodeling affects neuronal plasticity and discuss how the cytoskeleton is being targeted in an effort to promote plasticity and repair following traumatic injury in the central nervous system.
引用
收藏
页码:206 / 212
页数:7
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