Intrinsic mechanisms of neuronal axon regeneration

被引:360
|
作者
Mahar, Marcus [1 ,2 ]
Cavalli, Valeria [1 ,2 ]
机构
[1] Washington Univ, Sch Med, Dept Neurosci, Hope Ctr Neurol Disorders, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Ctr Regenerat Med, St Louis, MO 63130 USA
关键词
CENTRAL-NERVOUS-SYSTEM; SATELLITE GLIAL-CELLS; SPINAL-CORD-INJURY; RETINAL GANGLION-CELLS; UNFOLDED PROTEIN RESPONSE; PIONEER TRANSCRIPTION FACTORS; LEUCINE-ZIPPER KINASE; ADULT SENSORY NEURONS; PERIPHERAL-NERVE; IN-VIVO;
D O I
10.1038/s41583-018-0001-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Permanent disabilities following CNS injuries result from the failure of injured axons to regenerate and rebuild functional connections with their original targets. By contrast, injury to peripheral nerves is followed by robust regeneration, which can lead to recovery of sensory and motor functions. This regenerative response requires the induction of widespread transcriptional and epigenetic changes in injured neurons. Considerable progress has been made in recent years in understanding how peripheral axon injury elicits these widespread changes through the coordinated actions of transcription factors, epigenetic modifiers and, to a lesser extent, microRNAs. Although many questions remain about the interplay between these mechanisms, these new findings provide important insights into the pivotal role of coordinated gene expression and chromatin remodelling in the neuronal response to injury.
引用
收藏
页码:323 / 337
页数:15
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