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Camellia japonica Flower Extract and the Active Constituent Hyperoside Repair DNA Damage Through FUNDC1-Mediated
Hongqi Gao1,2, Jiahui Shi1, Guangtao Li2
1School of Pharmacy, Guangdong Engineering Technology Research Centre of Molecular Probe and Biomedicine Imaging, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Abstract:
Skin aging is closely related to mitochondrial dysfunction and cell cycle abnormalities, and developing intervention strategies targeting mitochondrial quality control is an important direction for anti-aging research. In this study, we investigated the anti-aging mechanism of Camellia japonica flower (CJF) extract and its active ingredient hyperoside based on a doxorubicin (DOX)-induced endogenous senescence model in human skin fibroblasts (HSFs). LC-MS proteomics analysis revealed that CJF extract and hyperoside specifically activated the FUNDC1-mediated mitochondrial autophagy pathway, significantly ameliorated the DOX-induced decrease in mitochondrial membrane potential and the accumulation of reactive oxygen species (ROS), and alleviated the cellular S-phase blockade and reversed the high expression of senescence-associated β-galactosidase (SA-β-gal). Further studies showed that the two cleared damaged mitochondria by enhancing mitochondrial autophagy and restoring cellular energy metabolism homeostasis while promoting type III collagen and elastin synthesis and repairing the expression of Claudin 1 related to skin barrier function. For the first time, the present study reveals the molecular mechanism of CJF extract in delaying skin aging by regulating the FUNDC1-dependent mitochondrial autophagy pathway, which provides a theoretical basis and a candidate strategy for developing novel anti-aging agents targeting mitochondrial quality control.
Insights
Camellia japonica flower extract and hyperoside combat skin aging by enhancing mitochondrial autophagy. This process improves cellular energy and skin barrier function, offering a novel anti-aging strategy.
Area of Science:
- Dermatology
- Cell Biology
- Biochemistry
Background:
- Skin aging is linked to mitochondrial dysfunction and cell cycle issues.
- Targeting mitochondrial quality control is a key area for anti-aging research.
Purpose of the Study:
- To investigate the anti-aging effects of Camellia japonica flower (CJF) extract and hyperoside.
- To elucidate the mechanism of CJF extract and hyperoside in a doxorubicin-induced senescence model in human skin fibroblasts (HSFs).
Main Methods:
- Doxorubicin (DOX)-induced endogenous senescence model in HSFs.
- LC-MS proteomics analysis.
- Assessment of mitochondrial membrane potential, reactive oxygen species (ROS) levels, cell cycle progression, and senescence-associated β-galactosidase (SA-β-gal) activity.
Main Results:
- CJF extract and hyperoside activated the FUNDC1-mediated mitochondrial autophagy pathway.
- They improved mitochondrial function, reduced ROS accumulation, and alleviated cell cycle arrest and SA-β-gal expression.
- Enhanced mitochondrial autophagy restored energy metabolism, promoted collagen and elastin synthesis, and repaired skin barrier function (Claudin 1).
Conclusions:
- CJF extract and hyperoside delay skin aging by regulating the FUNDC1-dependent mitochondrial autophagy pathway.
- This study provides a theoretical basis for developing new anti-aging agents targeting mitochondrial quality control.
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