EVIDENCE THAT DNA-DAMAGE IS A MEDIATE IN ULTRAVIOLET-B RADIATION - INDUCED-INHIBITION OF HUMAN GENE-EXPRESSION - ULTRAVIOLET-B RADIATION EFFECTS ON INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1) EXPRESSION

被引:31
|
作者
KRUTMANN, J [1 ]
BOHNERT, E [1 ]
JUNG, EG [1 ]
机构
[1] UNIV HEIDELBERG,MANNHEIM MED SCH,DEPT DERMATOL,HEIDELBERG,GERMANY
关键词
KERATINOCYTES; PHOTOIMMUNOLOGY; ADHESION MOLECULES; PYRIMIDINE DIMERS;
D O I
10.1111/1523-1747.ep12372947
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Expression of intercellular adhesion molecule-1 (ICAM-1) is a prerequisite for the capacity of cells to physically interact with leukocytes. Ultraviolet B radiation previously was found to inhibit interferon gamma- induced ICAM-1 expression in human keratinocytes by suppressing interferon gamma- mediated upregulation of ICAM-1 mRNA levels. Because ultraviolet B radiation induces photoproducts in cellular DNA, the potential role of ultraviolet B radiation - induced DNA damage in this system was assessed. For this purpose, cells from a normal donor were compared with cells from patients with xeroderma pigmentosum from complementation groups C and D. Xeroderma pigmentosum cells are defective in the removal of ultraviolet B radiation-induced DNA lesions, and thus lower ultraviolet B radiation doses are required to retain equivalent numbers of DNA photoproducts at a given time point after irradiation. In the present study, ultraviolet B radiation inhibited interferon gamma-induced ICAM-1 mRNA expression in primary human skin fibroblasts in a manner identical to that previously observed for keratinocytes. Comparative studies employing normal versus xeroderma pigmentosum fibroblasts revealed that in xeroderma pigmentosum fibroblasts, two- to threefold lower ultraviolet B radiation doses were required to achieve inhibition equivalent to that observed in normal fibroblasts. In irradiated normal cells, inhibition of interferon gamma-induced ICAM-1 mRNA expression was transient and restored 12 h after ultraviolet B radiation exposure. In contrast, in xeroderma pigmentosum complementation group D cells, no restoration could be observed for up to 48 h, but responsiveness was restored in xeroderma pigmentosum complementation group C cells after 24 h. These studies indicate that ultraviolet B radiation-induced inhibition of interferon gamma-mediated ICAM-1 expression involves the generation of DNA photoproducts.
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页码:428 / 432
页数:5
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