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Modulation of the UVA activation of haem oxygenase, collagenase and cyclooxygenase gene expression by epigallocatechin in human skin cells
- Source :
- FEBS Letters. 439:253-257
- Publication Year :
- 1998
- Publisher :
- Wiley, 1998.
-
Abstract
- We have investigated the modifying effects of epigallocatechin, a major polyphenolic constituent of green tea, on ultraviolet-A-activated gene expression in human fibroblasts and keratinocytes using the stress responsive enzymes: haem oxygenase-1, interstitial collagenase and cyclooxygenase-2. Although epigallocatechin strongly reduced ultraviolet-A-induced haem oxygenase-1 activation in skin-derived fibroblasts, the same compound activated collagenase and cyclooxygenase expression. In a keratinocyte cell line, ultraviolet-A-mediated haem oxygenase-1 over-expression was low and epigallocatechin failed to modulate it further. In contrast to the results with fibroblasts, ultraviolet-A activation of cyclooxygenase in keratinocytes was reduced by epigallocatechin. The results indicate that the effect of this green tea polyphenol on cellular stress responses is complex and may involve direct effects on signal transduction as well as changes that may be associated with its antioxidant activity.
- Subjects :
- Ultraviolet Rays
Collagenase
Biophysics
complex mixtures
Biochemistry
Catechin
Gene Expression Regulation, Enzymologic
Structural Biology
Gene expression
Tumor Cells, Cultured
Genetics
medicine
Humans
Collagenases
Molecular Biology
Cells, Cultured
Heat-Shock Proteins
Skin
Flavonoids
Regulation of gene expression
Tea
biology
Chemistry
food and beverages
Cell Biology
Fibroblasts
Ultraviolet-A
Cyclooxygenase
Cell biology
Epigallocatechin
Oxidative Stress
medicine.anatomical_structure
Prostaglandin-Endoperoxide Synthases
Cell culture
Hemoxygenase
Heme Oxygenase (Decyclizing)
biology.protein
Interstitial collagenase
Signal transduction
Keratinocyte
medicine.drug
Subjects
Details
- ISSN :
- 00145793
- Volume :
- 439
- Database :
- OpenAIRE
- Journal :
- FEBS Letters
- Accession number :
- edsair.doi.dedup.....fda15793d72aad347b842a66f119d54a