Modulation of the UVA activation of haem oxygenase, collagenase and cyclooxygenase gene expression by epigallocatechin in human skin cells

被引:47
作者
Soriani, M
Rice-Evans, C
Tyrrell, RM [1 ]
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Kings Coll London, Guys Hosp, London, England
[3] St Thomas Hosp, Sch Med & Dent, London, England
来源
FEBS LETTERS | 1998年 / 439卷 / 03期
关键词
epigallocatechin; ultraviolet-A; hemoxygenase; collagenase; cyclooxygenase; oxidative stress;
D O I
10.1016/S0014-5793(98)01387-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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-l 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 ton 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. (C) 1998 Federation of European Biochemical: Societies.
引用
收藏
页码:253 / 257
页数:5
相关论文
共 53 条
[1]  
AGARWAL R, 1992, CANCER RES, V52, P3582
[2]   PROTECTION AGAINST ULTRAVIOLET-B RADIATION-INDUCED EFFECTS IN THE SKIN OF SKH-1 HAIRLESS MICE BY A POLYPHENOLIC FRACTION ISOLATED FROM GREEN TEA [J].
AGARWAL, R ;
KATIYAR, SK ;
KHAN, SG ;
MUKHTAR, H .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1993, 58 (05) :695-700
[3]   STRUCTURE OF THE HUMAN CYCLO-OXYGENASE-2 GENE [J].
APPLEBY, SB ;
RISTIMAKI, A ;
NEILSON, K ;
NARKO, K ;
HLA, T .
BIOCHEMICAL JOURNAL, 1994, 302 :723-727
[4]   2 GENES CONTRIBUTE TO DIFFERENT EXTENTS TO THE HEME OXYGENASE ENZYME-ACTIVITY MEASURED IN CULTURED HUMAN SKIN FIBROBLASTS AND KERATINOCYTES - IMPLICATIONS FOR PROTECTION AGAINST OXIDANT STRESS [J].
APPLEGATE, LA ;
NOEL, A ;
VILE, G ;
FRENK, E ;
TYRRELL, RM .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1995, 61 (03) :285-291
[5]  
APPLEGATE LA, 1991, CANCER RES, V51, P974
[6]  
BAILEY JM, 1989, ADV PROSTAG THROMB L, V19, P450
[7]   The chemistry of tea flavonoids [J].
Balentine, DA ;
Wiseman, SA ;
Bouwens, LCM .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1997, 37 (08) :693-704
[8]  
BASUMODAK S, 1993, CANCER RES, V53, P4505
[9]   THE SKIN IMMUNE-SYSTEM - PROGRESS IN CUTANEOUS BIOLOGY [J].
BOS, JD ;
KAPSENBERG, ML .
IMMUNOLOGY TODAY, 1993, 14 (02) :75-78
[10]   Central role of ferrous/ferric iron in the ultraviolet B irradiation-mediated signaling pathway leading to increased interstitial collagenase (matrix-degrading metalloprotease (MMP)-1) and stromelysin-1 (MMP-3) mRNA levels in cultured human dermal fibroblasts [J].
Brenneisen, P ;
Wenk, J ;
Klotz, LO ;
Wlaschek, M ;
Briviba, K ;
Krieg, T ;
Sies, H ;
Scharffetter-Kochanek, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (09) :5279-5287