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iScience· 2026Q1

Repressed mTORC1 signaling and transient dendritic pruning support axonal regeneration in adult zebrafish

Anyi Zhang, Luca Masin, Steven Bergmans, Elena Putti et al.

Short summary

Adult zebrafish undergo transient dendritic pruning during axonal regeneration, which is suppressed by prolonged mTORC1 activation, delaying regrowth.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Axonal regeneration in adult zebrafish involves transient dendritic pruning.
  • Dendritic pruning occurs during axon elongation and reverses after brain reinnervation.
  • Suppression of mTORC1 signaling coincides with dendritic pruning and sustained axon growth.
  • Prolonging mTOR activation reduces pruning but delays axonal regrowth.

AI-generated from the title and abstract; the full text is not read.

Abstract

Dendrite degeneration is an early pathological feature following axonal damage, yet its role during successful axonal regeneration remains poorly understood. Using sparse labeling of retinal ganglion cells in adult zebrafish, we show that axonal regeneration is accompanied by a transient phase of dendritic pruning following optic nerve crush. Dendritic pruning occurs during axon elongation and is reversed after brain reinnervation. Although insulin–mTOR signaling is rapidly upregulated immediately after injury, it is subsequently suppressed, coinciding with dendritic pruning and sustained axonal growth. Prolonging mTOR activation through insulin treatment or direct pathway stimulation reduces dendritic pruning in an mTORC1-dependent manner but significantly delays axonal regrowth. Together, these findings identify dendritic remodeling as a temporally regulated component of axonal regeneration in zebrafish and reveal a functional trade-off between dendritic preservation and axon regrowth. This warrants further investigation on whether temporal modulation of dendritic remodeling could promote axonal regeneration in the mammalian CNS.

The authors' abstract, as published at the source. iScience, 2026 · DOI ↗

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Field: Cellular and Molecular Neuroscience

Cellular and Molecular NeuroscienceNeuroscience