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成年中枢神经系统受损轴突能否通过重现发育过程来实现再生?

Can injured adult CNS axons regenerate by recapitulating development?

作者信息

Hilton Brett J, Bradke Frank

机构信息

Laboratory for Axon Growth and Regeneration, German Centre for Neurodegenerative Diseases (DZNE), Sigmund-Freud-Strasse 27, 53127, Bonn, Germany

出版信息

Development. 2017 Oct 1;144(19):3417-3429. doi: 10.1242/dev.148312.

Abstract

In the adult mammalian central nervous system (CNS), neurons typically fail to regenerate their axons after injury. During development, by contrast, neurons extend axons effectively. A variety of intracellular mechanisms mediate this difference, including changes in gene expression, the ability to form a growth cone, differences in mitochondrial function/axonal transport and the efficacy of synaptic transmission. In turn, these intracellular processes are linked to extracellular differences between the developing and adult CNS. During development, the extracellular environment directs axon growth and circuit formation. In adulthood, by contrast, extracellular factors, such as myelin and the extracellular matrix, restrict axon growth. Here, we discuss whether the reactivation of developmental processes can elicit axon regeneration in the injured CNS.

摘要

在成年哺乳动物的中枢神经系统(CNS)中,神经元在受伤后通常无法再生其轴突。相比之下,在发育过程中,神经元能有效地延伸轴突。多种细胞内机制介导了这种差异,包括基因表达的变化、形成生长锥的能力、线粒体功能/轴突运输的差异以及突触传递的效能。反过来,这些细胞内过程与发育中的中枢神经系统和成年中枢神经系统之间的细胞外差异相关联。在发育过程中,细胞外环境引导轴突生长和回路形成。相比之下,在成年期,细胞外因子,如髓磷脂和细胞外基质,会限制轴突生长。在此,我们讨论发育过程的重新激活是否能在受损的中枢神经系统中引发轴突再生。

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