4.8 Article

Mitochondria Localize to Injured Axons to Support Regeneration

期刊

NEURON
卷 92, 期 6, 页码 1308-1323

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2016.11.025

关键词

-

资金

  1. National Institutes of Health - Office of Research Infrastructure Programs [P40 OD010440]
  2. James Hudson Brown - Alexander Brown Coxe Postdoctoral Fellowships in the Medical Sciences
  3. Department of Genetics Research Fellowship from Yale University
  4. NIH [R01NS098817, R01NS094219, R56AG050969]

向作者/读者索取更多资源

Axon regeneration is essential to restore the nervous system after axon injury. However, the neuronal cell biology that underlies axon regeneration is incompletely understood. Here we use in vivo, single-neuron analysis to investigate the relationship between nerve injury, mitochondrial localization, and axon regeneration. Mitochondria translocate into injured axons so that average mitochondria density increases after injury. Moreover, single-neuron analysis reveals that axons that fail to increase mitochondria have poor regeneration. Experimental alterations to axonal mitochondrial distribution or mitochondrial respiratory chain function result in corresponding changes to regeneration outcomes. Axonal mitochondria are specifically required for growth-cone migration, identifying a key energy challenge for injured neurons. Finally, mitochondrial localization to the axon after injury is regulated in part by dual-leucine zipper kinase 1 (DLK-1), a conserved regulator of axon regeneration. These data identify regulation of axonal mitochondria as a new cell-biological mechanism that helps determine the regenerative response of injured neurons.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据