PUBLICATION

Circadian per2 regulates the zebrafish central neuronal Mauthner cell axon regeneration via carboxypeptidase E

Authors
Fan, D.G., Li, K.Q., Zhao, Z.A., Zhou, J.H., Tang, X.H., Han, A.L., Song, Z., Hu, B.
ID
ZDB-PUB-260731-8
Date
2026
Source
Zoological research   47: 1353-1368 (Journal)
Registered Authors
Hu, Bing
Keywords
Axon regeneration, Circadian clock, Mauthner cells, Zebrafish
MeSH Terms
none
PubMed
42533585 Full text @ Zool Res
Abstract
Central nervous system (CNS) injuries often result in permanent neurological impairments or fatal outcomes. While circadian regulation is a key pathway affecting the regenerative capacity of peripheral neurons, the role of the intrinsic circadian clock in CNS axon regeneration remains elusive. Using a zebrafish larval model with disrupted circadian rhythms, we observed significant inhibition of CNS axon regeneration in a single Mauthner cell (M cell). Mutations or inhibition of the core circadian clock gene per2 in zebrafish larvae severely impaired axon regeneration and acoustically evoked escape movements. Time-of-day-dependent transcriptomic analysis revealed that per2 regulates genes involved in regeneration-related pathways, such as mitochondrial metabolism and Wnt signaling transduction. Furthermore, reverse transcription quantitative PCR and Western blot experiments indicated that the neurotrophic factor carboxypeptidase E (Cpe) exhibits robust circadian rhythmicity in wild-type but is significantly downregulated in per2-/- mutants. Cpe deficiency significantly suppressed axonal regeneration, whereas its overexpression enhanced regenerative capacity, thereby rescuing the axonal regeneration impairment in per2-/- mutants. Overall, our findings demonstrate the critical role of a stable circadian rhythm system and per2 in CNS regeneration, as well as the potential function of Cpe in promoting axon regeneration.
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