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固有机制调控轴突再生:整合素视角。

Intrinsic mechanisms regulating axon regeneration: an integrin perspective.

机构信息

Cambridge Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom.

出版信息

Int Rev Neurobiol. 2012;106:75-104. doi: 10.1016/B978-0-12-407178-0.00004-1.

Abstract

Adult central nervous system (CNS) axons fail to regenerate after injury because of inhibitory factors in the surrounding environment and a low intrinsic regenerative capacity. Axons in the adult peripheral nervous system have a higher regenerative capacity, due in part to the presence of certain integrins-receptors for the extracellular matrix. Integrins are critical for axon growth during the development of the nervous system but are absent from some adult CNS axons. Here, we discuss the intrinsic mechanisms that regulate axon regeneration and examine the role of integrins. As correct localization is paramount to integrin function, we further discuss the mechanisms that regulate integrin traffic toward the axonal growth cone.

摘要

成人中枢神经系统(CNS)轴突在受伤后无法再生,这是由于周围环境中的抑制因子和较低的内在再生能力。成人周围神经系统中的轴突具有更高的再生能力,部分原因是存在某些整合素——细胞外基质的受体。整合素在神经系统发育过程中对轴突生长至关重要,但在一些成年中枢神经系统轴突中缺失。在这里,我们讨论调节轴突再生的内在机制,并研究整合素的作用。由于正确的定位对整合素功能至关重要,我们进一步讨论了调节整合素向轴突生长锥运输的机制。

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