γ-glutamyltranspeptidase-dependent metabolism of 4-hydroxynonenal-glutathione conjugate

被引:27
作者
Enoiu, M
Herber, R
Wennig, R
Marson, C
Bodaud, H
Leroy, P
Mitrea, N
Siest, G
Wellman, M
机构
[1] Univ Nancy 1, Fac Pharm, EA 3117, F-54001 Nancy, France
[2] Univ Ctr Luxembourg, Natl Lab Hlth, Dept Toxicol, L-1011 Luxembourg, Luxembourg
[3] Univ Carol Davila, Fac Pharm, Dept Biochem, Bucharest 70139, Romania
关键词
4-hydroxynonenal; glutathione-4-hydroxynonenal conjugate; cysteinylglycine-4-hydroxynonenal conjugate; gamma-glutamyltranspeptidase; metabolism; cytotoxicity;
D O I
10.1006/abbi.2001.2633
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
A major pathway for detoxification of the highly reactive lipid peroxidation product, 4-hydroxy-2,3-trans-nonenal (HNE) is through the conjugation with glutathione (GSH). We have studied the metabolism of GS-HNE conjugate by the enzyme gamma-glutamyltranspeptidase (GGT) using its purified form, as well as a GGT-overexpressing fibroblast cell line (V79 GGT). Using mass spectrometry analysis we identified for the first time cysteinylglycine-HNE (CysGly-HNE) as the GGT metabolite of GS-HNE. Furthermore, the GGT-dependent metabolism of GS-HNE in the V79 GGT cell line was associated with a considerable increase of cytotoxicity as compared to a control cell line which does not express GGT (V79 Cl). The cytotoxic effect was dose- and time-dependent (100% cellular death at 200 muM GS-HNE after 24 h incubation) in V79 GGT cells, whereas no decrease of viability was observed in V79 C1 cells. A similar cytotoxic effect was obtained when cells were incubated directly with CysGly-HNE, demonstrating that this GGT-dependent metabolite unlike GS-HNE, exhibits cytotoxic properties. (C) 2001 Elsevier Science.
引用
收藏
页码:18 / 27
页数:10
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