PUBLICATION
Successful axonal regeneration is associated with intraneuronal metabolic reprogramming
- Authors
- Zhang, A., Bergmans, S., Van Dyck, A., Beckers, A., Moons, L., Masin, L.
- ID
- ZDB-PUB-251023-11
- Date
- 2025
- Source
- iScience 28: 113631 (Journal)
- Registered Authors
- Bergmans, Steven, Moons, Lieve, Van Dyck, Annelies, Zhang, Anyi
- Keywords
- Cellular neuroscience, Developmental neuroscience, Metabolic flux analysis
- MeSH Terms
- none
- PubMed
- 41126894 Full text @ iScience
Citation
Zhang, A., Bergmans, S., Van Dyck, A., Beckers, A., Moons, L., Masin, L. (2025) Successful axonal regeneration is associated with intraneuronal metabolic reprogramming. iScience. 28:113631.
Abstract
Unlike mammals, zebrafish can regrow axons after injury and restore circuit function in the central nervous system (CNS). Mitochondria have been identified as key players in this process, but how different metabolic pathways work together to sustain regeneration remains unclear. Using the RNA sequencing of adult zebrafish retinal ganglion cells after optic nerve crush injury, we found that oxidative phosphorylation is downregulated during axonal regrowth. Simultaneously, the thioredoxin antioxidant system was upregulated, likely to limit oxidative damage. Additionally, we observed an integrated upregulation of glycolysis and the pentose phosphate pathway during the initial regrowth phases, possibly to provide energy and supply NADPH for biosynthesis and antioxidant responses. Notably, several of these metabolic reprogramming signatures are also observed in the pro-regenerative mammalian model with Pten and Socs3 co-deletion. Inhibiting glycolysis and thioredoxin in zebrafish impairs axonal regrowth, suggesting that targeting these pathways could enhance CNS regeneration in mammals.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping