Antioxidants modulate acute solar ultraviolet radiation-induced NF-kappa-B activation in a human keratinocyte cell line

被引:150
作者
Saliou, C
Kitazawa, M
McLaughlin, L
Yang, JP
Lodge, JK
Tetsuka, T
Iwasaki, K
Cillard, J
Okamoto, T
Packer, L
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Membrane Bioenerget Grp, Berkeley, CA 94720 USA
[2] Ajinomoto Co Inc, Cent Res Labs, Kawasaki, Kanagawa 210, Japan
[3] Nagoya City Univ, Sch Med, Dept Mol Genet, Nagoya, Aichi 467, Japan
[4] INSERM, U456, Lab Biol Cellulaire & Vegetale, Rennes, France
关键词
antioxidants; silymarin; alpha-lipoic acid; NF-kappa B; AP-1; ultraviolet radiation; keratinocyte; skin cancer; erythema; free radical;
D O I
10.1016/S0891-5849(98)00212-3
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
Exposure of the human skin to ultraviolet radiation (UVR) leads to depletion of cutaneous antioxidants, regulation of gene expression and ultimately to the development of skin diseases. Although exogenous supplementation of antioxidants prevents UVR-induced photooxidative damage, their effects on components of cell signalling pathways leading to gene expression has not been clearly established. In the present study, the effects of the antioxidants alpha-lipoic acid, N-acetyl-L-cysteine (NAC) and the flavonoid extract silymarin were investigated for their ability to modulate the activation of the transcription factors nuclear factor kappa B (NF-kappa B) and activator protein-1 (AP-1) in HaCaT keratinocytes after exposure to a solar UV simulator. The activation of NF-kappa B and AP-1 showed a similar temporal pattern: activation was detected 2 h after UV exposure and maintained for up to 8 hr. To determine the capacity of activated NF-kappa B to stimulate transcription, NF-kappa B-dependent gene expression was measured using a reporter gene assay. The effects of the antioxidants on NF-kappa B and AP-1 activation were evaluated 3 h after exposure. While a high concentration of NAC could achieve a complete inhibition, low concentrations of alpha-lipoic acid and silymarin were shown to significantly inhibit NF-kappa B activation. In contrast AP-1 activation was only partially inhibited by NAC, and not at all by alpha-lipoic acid or silymarin. These results indicate that antioxidants such as alpha-lipoic acid and silymarin can efficiently modulate the cellular response to WR through their selective action on NF-kappa B activation. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:174 / 183
页数:10
相关论文
共 55 条
[1]   Chemoprevention of photocarcinogenesis [J].
Agarwal, R ;
Mukhtar, H .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 63 (04) :440-444
[2]  
Armstrong BK, 1996, CANCER SURV, V26, P133
[3]   THE ANTIOXIDANT ACTION OF N-ACETYLCYSTEINE - ITS REACTION WITH HYDROGEN-PEROXIDE, HYDROXYL RADICAL, SUPEROXIDE, AND HYPOCHLOROUS ACID [J].
ARUOMA, OI ;
HALLIWELL, B ;
HOEY, BM ;
BUTLER, J .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (06) :593-597
[4]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[5]   CONSTITUTIVE NF-KAPPA-B ACTIVATION, ENHANCED GRANULOPOIESIS, AND NEONATAL LETHALITY IN I-KAPPA-B-ALPHA-DEFICIENT MICE [J].
BEG, AA ;
SHA, WC ;
BRONSON, RT ;
BALTIMORE, D .
GENES & DEVELOPMENT, 1995, 9 (22) :2736-2746
[6]   UV-induced cutaneous photobiology [J].
Beissert, S ;
Granstein, RD .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1996, 31 (5-6) :381-404
[7]   INHIBITORY ACTION OF SILYMARIN OF LIPID PEROXIDE FORMATION IN RAT-LIVER MITOCHONDRIA AND MICROSOMES [J].
BINDOLI, A ;
CAVALLINI, L ;
SILIPRANDI, N .
BIOCHEMICAL PHARMACOLOGY, 1977, 26 (24) :2405-2409
[8]  
BOMBARDELLI E, 1991, Fitoterapia, V62, P115
[9]   NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE [J].
BOUKAMP, P ;
PETRUSSEVSKA, RT ;
BREITKREUTZ, D ;
HORNUNG, J ;
MARKHAM, A ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :761-771
[10]   SILYBIN DIHEMISUCCINATE PROTECTS AGAINST GLUTATHIONE DEPLETION AND LIPID-PEROXIDATION INDUCED BY ACETAMINOPHEN ON RAT-LIVER [J].
CAMPOS, R ;
GARRIDO, A ;
GUERRA, R ;
VALENZUELA, A .
PLANTA MEDICA, 1989, (05) :417-419