CALCIUM INDICATOR DYE QUIN2 INHIBITS HYDROGEN PEROXIDE-INDUCED DNA STRAND BREAK FORMATION VIA CHELATION OF IRON

被引:18
作者
BURKITT, MJ [1 ]
MILNE, L [1 ]
TSANG, SY [1 ]
TAM, SC [1 ]
机构
[1] UNIV ABERDEEN,DEPT CHEM,ABERDEEN AB9 2UE,SCOTLAND
关键词
D O I
10.1006/abbi.1994.1244
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
Exposure of HeLa cells to H2O2 at 4 degrees C caused DNA strand breakage which was prevented by the metal chelator 1,10-phenanthroline, but not by neocuproine. This is believed to indicate the participation of iron, rather than copper, in the formation of reactive hydroxyl radicals (.OH) from H2O2. The calcium indicator dye Quin2 also prevented H2O2-induced DNA fragmentation. The inhibition of oxidant-induced DNA fragmentation at 37 degrees C by Quin2 is often presented as evidence for the involvement of Ca2+-dependent endonucleases in damage. However, our finding that Quin2 inhibits DNA fragmentation at 4 degrees C led us to investigate the possibility that Quina may also inhibit DNA damage via its effects on metal-dependent OH formation. Using ESR spin trapping techniques and in vitro DNA oxidation measurements, we found that the binding of Fe by Ouin2 does not prevent OH formation, but inhibits DNA damage. This is believed to reflect the prevention of iron ion binding to DNA by Quina, directing OH generation to the bulk solution, thereby preventing damage. The Cu-Quina complex was found to be a poor catalyst of both OH formation and in vitro DNA damage. These findings suggest that the frequently reported protective effect of Quina toward DNA in cells exposed to oxidants may be due to the chelation of metal ions rather than the prevention of Ca2+-dependent endonuclease activation.(C) 1994 Academic Press, Inc.
引用
收藏
页码:321 / 328
页数:8
相关论文
共 50 条
[1]   COPPER-ION-DEPENDENT DAMAGE TO THE BASES IN DNA IN THE PRESENCE OF HYDROGEN-PEROXIDE [J].
ARUOMA, OI ;
HALLIWELL, B ;
GAJEWSKI, E ;
DIZDAROGLU, M .
BIOCHEMICAL JOURNAL, 1991, 273 :601-604
[2]  
ARUOMA OI, 1989, J BIOL CHEM, V264, P20509
[3]   OXYGEN-DEPENDENT MICROBIAL KILLING BY PHAGOCYTES .1. [J].
BABIOR, BM .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (12) :659-668
[4]  
BIRBOIM HC, 1993, ARCH BIOCHEM BIOPHYS, V294, P17
[5]  
BIRBOIM HC, 1986, CARCINOGENESIS, V7, P1511
[6]  
BOVERIS A, 1982, SUPEROXIDE DISMUTASE, V2, P15
[7]   IN THE ABSENCE OF CATALYTIC METALS ASCORBATE DOES NOT AUTOXIDIZE AT PH-7 - ASCORBATE AS A TEST FOR CATALYTIC METALS [J].
BUETTNER, GR .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 1988, 16 (01) :27-40
[8]   KINETICS OF REACTIONS OF LIGAND-SUBSTITUTED TRIS-(2,2'-BIPYRIDYL)IRON)2) COMPLEXES [J].
BURGESS, J ;
PRINCE, RH .
JOURNAL OF THE CHEMICAL SOCIETY, 1965, (NOV) :6061-&
[9]   ESR SPIN-TRAPPING STUDIES INTO THE NATURE OF THE OXIDIZING SPECIES FORMED IN THE FENTON REACTION - PITFALLS ASSOCIATED WITH THE USE OF 5,5-DIMETHYL-1-PYRROLINE-N-OXIDE IN THE DETECTION OF THE HYDROXYL RADICAL [J].
BURKITT, MJ .
FREE RADICAL RESEARCH COMMUNICATIONS, 1993, 18 (01) :43-57
[10]   THE AUTOXIDATION OF IRON(II) IN AQUEOUS SYSTEMS - THE EFFECTS OF IRON CHELATION BY PHYSIOLOGICAL, NONPHYSIOLOGICAL AND THERAPEUTIC CHELATORS ON THE GENERATION OF REACTIVE OXYGEN SPECIES AND THE INDUCEMENT OF BIOMOLECULAR DAMAGE [J].
BURKITT, MJ ;
GILBERT, BC .
FREE RADICAL RESEARCH COMMUNICATIONS, 1991, 14 (02) :107-123