Comparison of ultraviolet B-induced imbalance of antioxidant status in foreskin- and abdominal skin-derived human fibroblasts

被引:0
作者
Saguet, Thibaut
Robin, Sophie
Nicod, Laurence
Binda, Delphine
Viennet, Celine
Aubin, Francois
Coulomb, Bernard
Humbert, Philippe [1 ]
机构
[1] Univ Franche Comte, IFR Ingn Cellulaire & Tissulaire 133, EA 3183, Lab Ingn & Biol Cutanees, F-25041 Besancon, France
[2] Ctr Hosp Reg Univ, Dept Dermatol, F-25030 Besancon, France
[3] BioExigence, F-25000 Besancon, France
[4] Univ Franche Comte, EA 3924, F-25030 Besancon, France
[5] Univ Paris 05, Fac Chirurg Dent, EA2496, F-92120 Montrouge, France
关键词
age factor; antioxidant status; fibroblasts; human skin; ultraviolet B;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Ultraviolet B radiation (UVB) is involved in the development of deleterious cutaneous damage. Several changes could be attributed to UVB-induced reactive oxygen species attacks in fibroblasts. However dermal cells from young and adult skin could respond differently to oxidative stress. So antioxidant status and its consequences on cytotoxicity and apoptosis were compared in child foreskin fibroblasts (FF) and adult abdominal skin fibroblasts (AF) in response to UVB. Basal levels of lipid peroxidation tended to be higher in AF than in FF, which could be related to a reshaping of antioxidant defences (higher catalase and lower superoxide dismutase activities). AF and FF appeared to react similarly to high UVB doses as regards cytotoxicity and apoptosis which increased significantly 24h after exposure. The enhancement of cell death could be due to the inherent oxidative stress: glutathione appeared significantly decreased in both cell populations. As a consequence AF, but not FF, presented significantly increased levels of lipid peroxidation, which could be explained by the pre-cited differences of basal antioxidant defences. These results suggest that AF and FF do not respond to UVB by the same pathway.
引用
收藏
页码:368 / 374
页数:7
相关论文
共 54 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   Effects of solar radiation on cutaneous detoxification pathways [J].
Afaq, F ;
Mukhtar, H .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2001, 63 (1-3) :61-69
[3]   INHIBITION BY 5-SULFOSALICYLIC ACID OF THE GLUTATHIONE-REDUCTASE RECYCLING ASSAY FOR GLUTATHIONE ANALYSIS [J].
ALLEN, KGD ;
ARTHUR, JR .
CLINICA CHIMICA ACTA, 1987, 162 (02) :237-239
[4]  
ALLEN RG, 1995, J CELL PHYSIOL, V165, P576
[5]   Effects of ambient oxygen concentration on the growth and antioxidant defenses of human cell cultures established from fetal and postnatal skin [J].
Balin, AK ;
Pratt, L ;
Allen, RG .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (03) :257-267
[6]   FORMATION AND REDUCTION OF GLUTATHIONE-PROTEIN MIXED DISULFIDES DURING OXIDATIVE STRESS - A STUDY WITH ISOLATED HEPATOCYTES AND MENADIONE (2-METHYL-1,4-NAPHTHOQUINONE) [J].
BELLOMO, G ;
MIRABELLI, F ;
DIMONTE, D ;
RICHELMI, P ;
THOR, H ;
ORRENIUS, C ;
ORRENIUS, S .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (08) :1313-1320
[7]   Tissue-specific functions of individual glutathione peroxidases [J].
Brigelius-Flohé, R .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 27 (9-10) :951-965
[8]   OXIDATIVE STRESS AS A MEDIATOR OF APOPTOSIS [J].
BUTTKE, TM ;
SANDSTROM, PA .
IMMUNOLOGY TODAY, 1994, 15 (01) :7-10
[9]  
CARLBERG I, 1985, METHOD ENZYMOL, V113, P484
[10]   SUNBURN [J].
DANIELS, F ;
VANDERLE.JC ;
JOHNSON, BE .
SCIENTIFIC AMERICAN, 1968, 219 (01) :38-&