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Updated: Aug 7, 2026

Studying Chronic Exposure of Mice to Ultraviolet B Radiation
Published on: August 19, 2025
Protective Effects of Donkey Milk-Derived Exosomes Against UVB-Induced Skin Photoaging via Regulation of DNA Damage
Abstract:
Prolonged exposure to UVB radiation accelerates skin photoaging by inducing DNA damage, promoting collagen degradation, and triggering cellular senescence. There is a growing interest in identifying effective natural interventions to prevent or mitigate these adverse effects. This study investigated the protective role and underlying mechanisms of donkey milk-derived exosomes (DM-Exos) against UVB-induced skin aging using both in vitro skin cell models and in vivo mouse models. The results demonstrated that DM-Exos significantly reduced UVB-induced cellular senescence, as evidenced by decreased β-galactosidase activity and downregulation of senescence-associated genes. DM-Exos also attenuated intracellular ROS production and reduced DNA damage markers (γ-H2AX and 8-OHdG) both in vitro and in vivo. Transcriptomic analysis further revealed that DM-Exos mitigated UVB-induced alterations in pathways related to cellular senescence, DNA damage, cell proliferation, and response to UV radiation, which were corroborated by qPCR validation of key aging-related genes. These findings underscore the potential of DM-Exos as a promising natural agent for protecting against UVB-induced skin aging and maintaining overall skin health.
Insights
Donkey milk-derived exosomes (DM-Exos) show promise in protecting skin from UVB damage. These exosomes reduce cellular senescence and DNA damage, offering a natural approach to combat skin aging.
Area of Science:
- Dermatology
- Biotechnology
- Molecular Biology
Background:
- UVB radiation accelerates skin photoaging, causing DNA damage and cellular senescence.
- Natural interventions are sought to mitigate UVB-induced skin aging effects.
Purpose of the Study:
- To investigate the protective effects of donkey milk-derived exosomes (DM-Exos) against UVB-induced skin aging.
- To elucidate the underlying mechanisms of DM-Exos in preventing skin aging.
Main Methods:
- In vitro skin cell models and in vivo mouse models were used.
- Assessed cellular senescence markers (β-galactosidase activity, senescence-associated genes).
- Measured reactive oxygen species (ROS) production and DNA damage markers (γ-H2AX, 8-OHdG).
- Performed transcriptomic analysis and qPCR validation.
Main Results:
- DM-Exos significantly reduced UVB-induced cellular senescence and ROS production.
- DM-Exos attenuated DNA damage markers in vitro and in vivo.
- Transcriptomic analysis revealed DM-Exos modulated key aging-related pathways.
Conclusions:
- Donkey milk-derived exosomes demonstrate significant protective potential against UVB-induced skin aging.
- DM-Exos offer a promising natural strategy for maintaining skin health and preventing photoaging.
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