The Effects of Epigallocatechin Gallate on Ultraviolet B Irradiated Cultured Human Skin Fibroblasts.
- Author:
Byung Wook SEO
1
;
Sung Il SUH
;
Won Ki BAEK
;
Min Ho SUH
;
Sang Pyo KIM
;
Tae Young JUNG
;
Jae We CHO
;
Byung Chun KIM
;
Kyu Suk LEE
;
Young Wook RYOO
Author Information
1. Department of Dermatology, School of Medicine, Keimyung University, Taegu, Korea. ryoo111@dsmc.or.kr
- Publication Type:Original Article
- Keywords:
Epigallocatechin gallate(EGCG);
UVB;
Dermal fibroblast
- MeSH:
Blotting, Western;
Cardiovascular Diseases;
Catechin;
Cell Death;
Cell Membrane;
Cell Survival;
Cyclin D1;
Fibroblasts*;
Flavonoids;
Free Radicals;
Genes, jun;
Humans*;
Lipid Peroxidation;
Membranes;
Propidium;
Skin*;
Trypan Blue
- From:Korean Journal of Dermatology
2001;39(5):519-528
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: The main polyphenol components in green tee are (-)-epicatechin, (-)-epigallocatechin, (-)-epicatechin gallate and (-)-epigallocatechin gallate (EGCG). It is well known that flavonoids such as catechins can be protective against inflammatory and cancer and cardiovascular diseases. These protective effects are largely due to their inhibition of some enzymes and antioxidative activities by scavenging free radicals. Ultraviolet(UV) exposure of the skin, particulary UVB (290-320nm), causes adverse biological effects, including alterations in cutaneous immune cells, photoaging and photocarcinogenesis. Several studies have shown that EGCG afforded protection against UVB-induced inflammatory responses and photocarcinogenesis in murine models. OBJECTIVE AND METHODS: In this study, we investigated the effects of EGCG on UVB irradiated human skin fibroblasts using viability test, thiobarbituric acid assay, propidium iodide(PI) stain, and western blot analyses and RT-PCR. RESULTS: Cell survival curves after UVB irradiation showed dose dependent decrement pattern by trypan blue exclusion assay. Only 42% of dermal fibroblasts survived at 150 mJ/cm2 UVB irradiation. The damage was associated with cell membrane lipid peroxidation, as shown by accumulation malondialdehyde(MDA). By pre-cultivation with EGCG (50nmol), a significant preventive effect was noted on the increase in the absolute number of surviving cells(up to 81.5% of cells survived) and the levels of MDA markedly decreased. Morphological changes associated with apoptotic cell death were easily distinguished by PI stain. Bases on our finding, we investgated the regulation of p53, p21, bax, bcl-2, cyclin D1, E, Cdk2, and PARP proteins by western blot analyses. The expression p53 protein was elevated by following UVB exposure which was inhibited by EGCG treatment. Using RT-PCR, the transcription of p53, fas and jun gene showed similar results which obtained by western blot analyses. CONCLUSION: EGCG, which have newly accepted as a potential UV protection properties, is effective membrane peroxidation inhibitor and prevent apoptotic changes when present in relevant concentration at the site of action beginning and during UVB irradiation. And the protective mechanism of EGCG against UVB-induced cell damage maybe, at least in part, related with p53, fas and jun pathway.
