Effects of ultraviolet A and antioxidant defense in cultured fibroblasts and keratinocytes
Abstract
Lipid peroxidation, measured by the thiobarbituric acid‐reactive substances assay, was evaluated for cultured human skin fibroblasts and keratinocytes exposed to ultraviolet A radiation (320–400 nm, UVA). Peroxidation increases with increasing UVA doses and is much lower for keratinocytes than for fibroblasts. Immediate UVA‐induced cytotoxicity, monitored by the trypan blue exclusion assay, is also lower for keratinocytes. Thus, cultured human skin keratinocytes are less sensitive than fibroblasts to the immediate deleterious effects of UVA with respect to membrane damage and lipid peroxidation. As a first attempt to understand this lower sensitivity of keratinocytes, basal levels of antioxidant defenses including total glutathione, superoxide dismutase, glutathione peroxidase and catalase were evaluated in both keratinocytes and fibroblasts from the same donors. We failed to correlate this lower susceptibility of keratinocyte to UVA‐induced lipid peroxidation and cytotocixity with a higher antioxidant status.
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The molecular mechanisms of UV-induced apoptosis of keratinocytes include generation of ROS.
“The molecular mechanisms of UV-induced apoptosis of keratinocytes include direct DNA damage (intrinsic), clustering of death receptors on the cell surface (extrinsic), and generation of ROS.”
From Molecular Mechanisms of UV-Induced Apoptosis and Its Effects on Skin Residential Cells: The Implication in UV-Based Phototherapy (2013) · cites this paper as [48]
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Lee, C.-H., Wu, S.-B., Hong, C.-H., Yu, H.-S., & Wei, Y.-H. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms14036414 · Cited by 271 · see citing works
Courdavault, S., Baudouin, C., Charveron, M., Favier, A., Cadet, J., & Douki, T. (2004) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2004.07.011 · Cited by 145 · see citing works
Marrot, L., Belaïdi, J. P., Jones, C., Perez, P., Meunier, J. R., Riou, L., & Sarasin, A. (2003) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2003.12422.x · Cited by 70 · see citing works
- Authors
- Moysan, A., Clément‐Lacroix, P., Michel, L., Dubertret, L., & Morlière, P.
- Affiliations
- Inserm (FR)
- Corresponding author
- Moysan, A.
- ORCID
- Michel, L.
- Venue
- Photodermatology, Photoimmunology & Photomedicine
- Publisher
- Wiley
- Published
- 1995-10-12
- Volume
- 11
- Issue
- 5-6
- Pages
- 192-197
- ISSN
- 0905-4383 (ISSN-L)
- 1600-0781
- OpenAlex
- W2077754999
- Cited by
- 47
- References
- 0
- Citations by year
- 2023: 1 · 2022: 1 · 2020: 1 · 2017: 3 · 2016: 3 · 2015: 1 · 2014: 3 · 2013: 3 · 2012: 2
- FWCI
- 2.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Photodermatology Photoimmunology & Photomedicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Fondation de France
- Topics
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Keywords
- ultraviolet A radiation, keratinocytes, dermal fibroblasts, lipid peroxidation, antioxidant defense, glutathione, superoxide dismutase, glutathione peroxidase, catalase, membrane damage, photoaging
- MeSH terms
- Adult, Antioxidants, Catalase, Cells, Cultured, Fibroblasts, Glutathione, Glutathione Peroxidase, Humans, Middle Aged, Skin, Superoxide Dismutase, Ultraviolet Rays, Lipid Peroxidation, Keratinocytes, Thiobarbituric Acid Reactive Substances
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