Using MT-/- mice to study metallothionein and oxidative stress

被引:40
作者
Conrad, CC
Grabowski, DT
Walter, CA
Sabia, M
Richardson, A
机构
[1] S Texas Vet Hlth Care Syst, Geriatr Res Educ & Clin Ctr, San Antonio, TX 78284 USA
[2] Univ N Texas, Hlth Sci Ctr, Dept Mol Biol & Immunol, Ft Worth, TX 76107 USA
[3] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78285 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Physiol, San Antonio, TX 78285 USA
基金
美国国家卫生研究院;
关键词
metallothionein; knockout mice; liver; DNA oxidation; lipid peroxidation; protein oxidation; free radicals;
D O I
10.1016/S0891-5849(99)00263-4
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
Mice with null mutations for metallothionein genes MT-1 and MT-2 were used to study the role that metallothionein plays in protecting cellular targets in vivo from oxidative stress. Wild-type (MT+/+) and MT-null (MT-/-) mice were treated with either saline or zinc and exposed to two types of oxidative stress: gamma-irradiation or 2-nitropropane. There was no alteration in the antioxidant defense system (superoxide dismutase, catalase, or glutathione peroxidase and glutathione levels) to compensate for the lack of the metallothionein in the MT-/- mice. The amount of oxidative damage to liver DNA, lipids, and proteins were similar for the MT-/- and MT+/+ mice even though the levels of metallothionein in the livers of the saline- or zinc-pretreated MT+/+ mice were 5- to 100-fold greater than found in the MT-/- mice. To determine if metallothionein can protect mice from the lethal effects of ionizing radiation, the mean survivals of MT-/- and MT+/+ mice exposed to whole body gamma-irradiation were measured and found to be similar. However, the mean survival increased significantly after zinc pretreatment for both the MT-/- and MT+/+ mice. These results demonstrate that tissue levels of metallothionein do not protect mice in vivo against oxidative stress. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:447 / 462
页数:16
相关论文
共 97 条
[71]   TARGETING AND GERM-LINE TRANSMISSION OF A NULL MUTATION AT THE METALLOTHIONEIN I-LOCI AND II-LOCI IN MOUSE [J].
MICHALSKA, AE ;
CHOO, KHA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :8088-8092
[72]   LEVELS OF GLUTATHIONE, GLUTATHIONE REDUCTASE AND GLUTATHIONE S-TRANSFERASE ACTIVITIES IN RAT LUNG AND LIVER [J].
MORON, MS ;
DEPIERRE, JW ;
MANNERVIK, B .
BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 582 (01) :67-78
[73]   BENZYL VIOLOGEN INACTIVATION OF RAT-LIVER GLUTAMINE-SYNTHETASE [J].
MURIANA, FJG ;
RELIMPIO, AM .
JOURNAL OF BIOCHEMISTRY, 1993, 113 (06) :738-741
[74]   ASSAY FOR LIPID PEROXIDES IN ANIMAL-TISSUES BY THIOBARBITURIC ACID REACTION [J].
OHKAWA, H ;
OHISHI, N ;
YAGI, K .
ANALYTICAL BIOCHEMISTRY, 1979, 95 (02) :351-358
[75]  
OLEINICK N L, 1988, NCI (National Cancer Institute) Monographs, P225
[76]   Effects of gamma radiation on levels of brain metallothionein and lipid peroxidation in transgenic mice [J].
Ono, S ;
Cai, L ;
Cherian, MG .
RADIATION RESEARCH, 1998, 150 (01) :52-57
[77]   MT-III, A BRAIN-SPECIFIC MEMBER OF THE METALLOTHIONEIN GENE FAMILY [J].
PALMITER, RD ;
FINDLEY, SD ;
WHITMORE, TE ;
DURNAM, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6333-6337
[78]   INDUCTION OF A NEW METALLOTHIONEIN ISOFORM (MT-IV) OCCURS DURING DIFFERENTIATION OF STRATIFIED SQUAMOUS EPITHELIA [J].
QUAIFE, CJ ;
FINDLEY, SD ;
ERICKSON, JC ;
FROELICK, GJ ;
KELLY, EJ ;
ZAMBROWICZ, BP ;
PALMITER, RD .
BIOCHEMISTRY, 1994, 33 (23) :7250-7259
[79]   METALLOTHIONEIN AND ITS RELATIONSHIP TO METABOLISM OF DIETARY ZINC IN RATS [J].
RICHARDS, MP ;
COUSINS, RJ .
JOURNAL OF NUTRITION, 1976, 106 (11) :1591-1599
[80]   AGING OF THE LIVER - PROTEOLYSIS OF OXIDATIVELY MODIFIED GLUTAMINE-SYNTHETASE [J].
SAHAKIAN, JA ;
SZWEDA, LI ;
FRIGUET, B ;
KITANI, K ;
LEVINE, RL .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1995, 318 (02) :411-417