4.8 Article

The Mammalian-Specific Protein Armcx1 Regulates Mitochondrial Transport during Axon Regeneration

Journal

NEURON
Volume 92, Issue 6, Pages 1294-1307

Publisher

CELL PRESS
DOI: 10.1016/j.neuron.2016.10.060

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Funding

  1. International Foundation for Research in Paraplegia
  2. Wings for Life Spinal Cord Research Foundation
  3. Swiss National Science Foundation
  4. Dr. Miriam and Sheldon G. Adelson Medical Research Foundation [R01EY021242]
  5. 3R Research Foundation Switzerland [R01GM069808, 129-11]
  6. NIH [P30 HD018655, P30EY012196]

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Mitochondrial transport is crucial for neuronal and axonal physiology. However, whether and how it impacts neuronal injury responses, such as neuronal survival and axon regeneration, remain largely unknown. In an established mouse model with robust axon regeneration, we show that Armcx1, a mammalian-specific gene encoding a mitochondria-localized protein, is upregulated after axotomy in this high regeneration condition. Armcx1 overexpression enhances mitochondrial transport in adult retinal ganglion cells (RGCs). Importantly, Armcx1 also promotes both neuronal survival and axon regeneration after injury, and these effects depend on its mitochondrial localization. Furthermore, Armcx1 knockdown undermines both neuronal survival and axon regeneration in the high regenerative capacity model, further supporting a key role of Armcx1 in regulating neuronal injury responses in the adult central nervous system (CNS). Our findings suggest that Armcx1 controls mitochondrial transport during neuronal repair.

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