Genes· 2026Q2
Nighttime Blue Light Promotes Lipid Accumulation and Shortens Lifespan via DAF-16/SOD-3-Mediated Oxidative Stress in C. elegans
- 0citations
- Q2SCImago
- 2026year
Short summary
Nighttime blue light exposure in C. elegans significantly increases lipid accumulation and shortens lifespan by promoting oxidative stress, mediated by the DAF-16/SOD-3 signaling pathway.
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Key points
- Nighttime blue light exposure increases lipid levels and accelerates aging in C. elegans.
- Blue light exposure elevates reactive oxygen species (ROS) and lipofuscin, markers of oxidative stress.
- The DAF-16 transcription factor translocates to the nucleus, while SOD-3 expression decreases under blue light.
- Knocking out sod-3 worsens blue light-induced lipid accumulation and lifespan shortening.
AI-generated from the title and abstract; the full text is not read.
Abstract
Background: Light, a crucial abiotic factor, consistently modulates organismal physiological activities. However, artificial light at night (ALAN) presents a considerable challenge. The widespread use of blue-light-rich light-emitting diodes (LEDs) in electronic products contributes to “blue light enrichment”. With population aging, the prevalence of obesity among older adults was expected to continue to increase. ALAN potentially induced obesity and shortened lifespan. However, the underlying pathogenic mechanism remains poorly understood. Methods: In this study, we investigated the effects of blue light on aging and lipid accumulation. Transcriptome and proteome analyses were performed to explore the potential regulatory mechanisms. Based on the enrichment results, we measured markers of lipid peroxidation and oxidative stress in Caenorhabditis elegans (C. elegans). We also conducted gene knockout experiments to verify the core regulatory genes. Results: The results showed that nighttime blue light induced lipid accumulation and aging in animals. Transcriptome and proteome analyses revealed that these effects might involve lipid transport, fatty acid metabolism, and oxidoreductase activity. Based on the enrichment results, we measured markers of lipid peroxidation and oxidative stress in C. elegans. Nighttime blue light exposure increased ROS, lipofuscin, lipid levels, and DAF-16 nuclear translocation, and decreased daf-16/sod-3. Notably, sod-3 knockout further exacerbated nighttime blue-light-induced lipid accumulation and lifespan shortening. Conclusions: In conclusion, our observations in C. elegans suggest that blue light is associated with altered DAF-16/SOD-3 signaling and that SOD-3 appears to contribute to protection against blue-light-induced stress. These findings provide experimental evidence from C. elegans supporting minimizing unnecessary nighttime lighting, particularly blue light exposure.
The authors' abstract, as published at the source. Genes, 2026 · DOI ↗
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AgingBiochemistry, Genetics and Molecular Biology