Dihydroxyacetone, the active browning ingredient in sunless tanning lotions, induces DNA damage, cell-cycle block and apoptosis in cultured HaCaT keratinocytes

被引:62
作者
Petersen, AB
Wulf, HC
Gniadecki, R
Gajkowska, B
机构
[1] Bispebjerg Hosp, Dept Dermatol, DK-2400 Copenhagen NV, Denmark
[2] Polish Acad Sci, Med Res Ctr, Lab Cell Ultrastruct, Warsaw, Poland
关键词
dihydroxyacetone; non-enzymatic glycation; DNA damage; cell cycle block; apoptosis;
D O I
10.1016/j.mrgentox.2004.03.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dihydroxyacetone (DHA), the active substance in sunless tanning lotions reacts with the amino groups of proteins to form a brown-colored complex. This non-enzymatic glycation, known as the Maillard reaction, can also occur with free amino groups in DNA, raising the possibility that DHA may be genotoxic. To address this issue we investigated the effects of DHA on cell survival and proliferation of a human keratinocyte cell line, HaCaT. Dose- and time-dependent morphological changes, chromatin condensation, cytoplasmic budding and cell detachment were seen in cells treated with DHA. Several dead cells were observed after long-time (24 h) incubation with 25 mM DHA or more. Furthermore, an extensive decline in proliferation was observed 1 day after DHA exposure for 24 h. When applied in different concentrations (5-50 mM) and for different time periods (1, 3 or 24h) DHA caused a G(2)/M block after the cyclin B-1 restriction point. Exit from this cell-cycle block was associated with massive apoptosis, as revealed by a clonogenic assay, TUNEL staining and electron microscopy. Furthermore, DHA caused DNA damage as revealed by the alkaline comet assay. Preincubation with antioxidants prevented the formation of DNA strand breaks. The DHA toxicity may be caused by direct redox reactions, with formation of ROS as the crucial intermediates. The genotoxic capacity of DHA raises a question about the long-term clinical consequences of treatment of the skin with this commonly used compound. (C) 2004 Elsevier B.V. All rights reserved.
引用
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页码:173 / 186
页数:14
相关论文
共 36 条
[1]  
AKIN FJ, 1984, J ENVIRON PATHOL TOX, V5, P349
[2]   Reconstruction of a human skin equivalent using a spontaneously transformed keratinocyte cell line (HaCaT) [J].
Boelsma, E ;
Verhoeven, MCH ;
Ponec, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (04) :489-498
[3]   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
[4]  
BROWNLEE M, 1988, NEW ENGL J MED, V318, P1315
[5]   MODIFICATION OF DNA BY REDUCING SUGARS - A POSSIBLE MECHANISM FOR NUCLEIC-ACID AGING AND AGE-RELATED DYSFUNCTION IN GENE-EXPRESSION [J].
BUCALA, R ;
MODEL, P ;
CERAMI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (01) :105-109
[6]  
FINOT PA, 1982, DIABETES S3, V31, P22, DOI DOI 10.2337/DIAB.31.3.S22
[7]  
Fusenig NE, 1998, MOL CARCINOGEN, V23, P144, DOI 10.1002/(SICI)1098-2744(199811)23:3<144::AID-MC3>3.0.CO
[8]  
2-U
[9]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[10]   INVESTIGATIVE STUDIES WITH THE SKIN COLORING AGENTS DIHYDROXYACETONE AND GLYOXAL - PRELIMINARY REPORT [J].
GOLDMAN, L ;
BARKOFF, J ;
BLANEY, D ;
NAKAI, T ;
SUSKIND, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1960, 35 (03) :161-164