Singlet oxygen is an early intermediate in cytokine-dependent ultraviolet-A induction of interstitial collagenase in human dermal fibroblasts in vitro

被引:107
作者
Wlaschek, M
Wenk, J
Brenneisen, P
Briviba, K
Schwarz, A
Sies, H
ScharffetterKochanek, K
机构
[1] UNIV COLOGNE, DEPT DERMATOL, D-50924 COLOGNE, GERMANY
[2] UNIV DUSSELDORF, DEPT PHYSIOL CHEM 1, D-4000 DUSSELDORF, GERMANY
[3] UNIV MUNSTER, CELL BIOL LAB, LBI, DVS, DEPT DERMATOL, D-4400 MUNSTER, GERMANY
关键词
singlet oxygen; UV response; cytokines; connective tissue; collagenase;
D O I
10.1016/S0014-5793(97)00919-8
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
Ultraviolet (UV) A irradiation of human dermal fibroblasts elicits an increase in specific mRNA amounts and bioactivities of the cytokines IL-1 alpha, IL-1 beta, and IL-6, These effects are enhanced in deuterium oxide-based medium and are diminished in the presence of non-toxic concentrations of sodium azide, Furthermore, generating singlet oxygen outside the cells by irradiation of rose bengal-coated resin particles with visible light (lambda > 450 nm) results in the induction of interstitial collagenase, IL-1 and IL-6, similar to the response observed with WA irradiation, These observations suggest that singlet oxygen is an early intermediate in the signaling pathway of IL-1 and IL-6 mediating UVA induction of interstitial collagenase (E.C. 3.4.24.7). Furthermore, singlet oxygen appears to initiate this complex UV response at the cell membrane. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:239 / 242
页数:4
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