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Neuronal cytoskeleton in synaptic plasticity and regeneration

机译:神经元细胞骨架在突触可塑性和再生中。

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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.
机译:在发育过程中,轴突生长锥和树突的动态变化对于基础轴突-树突接触的初步探索运动和最终形成功能性突触是必要的。在成人中枢神经系统中,通过突触前和突触后区室的形态和分子重排保留了令人印象深刻的可塑性,这是突触通路增强或减弱的基础。可塑性受可容许的和抑制性的细胞外信号的相互作用的调节,该信号通过突触上的受体发出信号以调节发育可塑性的关键时期的关闭,以及可塑性对成年人的经验和活动的响应发生急剧变化。突触可塑性的分子基础已得到积极研究,很明显,细胞骨架是影响可塑性的许多线索的关键底物。限制突触可塑性的许多线索在受伤的成年中枢神经系统中表现出残余活性,并通过靶向细胞骨架来限制再生生长。在这里,我们回顾了有关细胞骨架重塑如何影响神经元可塑性的一些最新见解,并讨论了如何针对细胞骨架进行靶向,以促进中枢神经系统创伤后的可塑性和修复。

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