Oxidative Stress Signaling and Regenerative Responses in a Larval Zebrafish Model of Retinal Light Damage

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Authors: Ignacio Babiloni-Chust, Luigi Donato, Samuele Sartori, Matthias Carl, Darin Zerti, Carmela Rinaldi, Vincenzo Flati, Marco Feligioni, Rosalia D'Angelo, Rita Maccarone, Lucia Poggi
Cited by: 1

Abstract

The zebrafish (Danio rerio) is a widely used model for studying retinal regeneration. In adults, light-induced retinal damage (LIRD) serves as an environmental phototoxic stressor that induces photoreceptor degeneration and regenerative responses, whereas larval models remain comparatively underexplored. In this study, we validate a larval LIRD paradigm as a versatile system for studying acute phototoxic injury and early regeneration-associated transcriptomic responses. Using high-throughput RNA sequencing, we profiled retinal transcriptional changes 48 hours post-LIRD and complemented these findings with targeted pharmacological modulation of redox signaling. Larval LIRD induced robust activation of canonical apoptotic and regeneration-associated pathways, recapitulating key features of adult LIRD models while engaging previously underexplored gene-regulatory networks. Among these, pathways related to oxidative stress responses, antioxidant enzymes, and oxygen metabolism were prominently regulated. Functional attenuation of oxidative stress using N-acetylcysteine reduced phototoxic injury-induced apoptosis and proliferation, while inflammatory markers remained largely unaffected. Conversely, subtoxic intra-retinal hydrogen peroxide exposure was sufficient to induce proliferative markers without eliciting apoptosis response. At the signaling level, modulation of oxidative stress influenced components of growth-associated signaling pathways activated during early injury response. Together, these findings support a role for oxidative stress as a key component of early injury-associated signaling in larval retinal regeneration. This study validates larval LIRD as a versatile experimental model and provides a transcriptomic resource for investigating redox-associated mechanisms underlying retinal injury and repair.

Fields of Study & Subjects

Retinal Development and Disorders Corneal Surgery and Treatments Retinal and Macular Surgery

Publication details

Journal / source
Preprints.org
Publisher
MDPI AG
Publication date
9 February 2026
Document type
Preprint