Selective expression of detoxifying glutathione transferases in mouse colon: effect of experimental colitis and the presence of bacteria

被引:13
作者
Edalat, M
Mannervik, B
Axelsson, LG
机构
[1] Karolinska Inst, Div Mol Pathol, Ctr Microbiol & Tumor Biol, Gastrobiol Unit, S-17177 Stockholm, Sweden
[2] Uppsala Univ, Ctr Biomed, Dept Biochem, S-75123 Uppsala, Sweden
关键词
glutathione transferase; dextran sulfate sodium; inflammatory bowel disease; intestinal flora; animal model;
D O I
10.1007/s00418-004-0688-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glutathione transferases (GSTs) play a central role in the cellular defense against harmful endogenous compounds and xenobiotics in mouse and man. The gastrointestinal channel is constantly exposed to bacteria, bacterial products, and xenobiotics. In the present study the distribution of alpha, mu, and pi class GSTs was examined immunohistologically in the colon of conventional and germ-free (GF) mice subjected to experimental colitis. The tissues samples were from conventional mice with and without colitis induced by dextran sulfate sodium (DSS); GF mice treated with DSS or carrageenan; and GF mice inoculated with normal mouse bacterial flora as well as with Lactobacillus GG. In conventional as well as in GF mice the mu and pi class GSTs showed reduced intestinal expression when colitis was induced. In contrast, the level of GSTs reacting with antibodies directed against the alpha class, in particular mGST A4-4, was elevated after induction of inflammation. Of special interest is mGST A4-4 because of its high catalytic activity with toxic products of lipid peroxidation. In the colon of conventionalized GF mice that were given mouse intestinal flora, the mGST A4-4 expression was increased with time for several weeks, but then showed a decrease to a normal level. Additionally, the inoculation of GF mice with Lactobacillus GG induced all the intestinal GSTs studied.
引用
收藏
页码:151 / 159
页数:9
相关论文
共 56 条
[1]  
ALDER V, 1999, EMBO J, V18, P1321
[2]  
Axelsson LG, 1997, GASTROENTEROLOGY, V112, pA925
[3]   Experimental colitis induced by dextran sulphate sodium in mice: beneficial effects of sulphasalazine and olsalazine [J].
Axelsson, LG ;
Landstrom, E ;
Bylund-Fellenius, AC .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 1998, 12 (09) :925-934
[4]  
Axelsson LG, 1996, MICROB ECOL HEALTH D, V9, P225, DOI 10.1002/(SICI)1234-987X(199609)9:5<225::AID-MEH431>3.3.CO
[5]  
2-R
[6]   Dextran sulfate sodium (DSS) induced experimental colitis in immunodeficient mice: Effects in CD4(+)-cell depleted, athymic and NK-cell depleted SCID mice [J].
Axelsson, LG ;
Landstrom, E ;
Goldschmidt, TJ ;
Gronberg, A ;
BylundFellenius, AC .
INFLAMMATION RESEARCH, 1996, 45 (04) :181-191
[7]  
AXELSSON LG, 1999, MICROECOL THER, V28, P327
[8]  
AXELSSON LG, 1996, THESIS FS TECHNOLOGY, P62
[9]   DETOXICATION OF BASE PROPENALS AND OTHER ALPHA,BETA-UNSATURATED ALDEHYDE PRODUCTS OF RADICAL REACTIONS AND LIPID-PEROXIDATION BY HUMAN GLUTATHIONE TRANSFERASES [J].
BERHANE, K ;
WIDERSTEN, M ;
ENGSTROM, A ;
KOZARICH, JW ;
MANNERVIK, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (04) :1480-1484
[10]   Identification, characterization, and crystal structure of the omega class glutathione transferases [J].
Board, PG ;
Coggan, M ;
Chelvanayagam, G ;
Easteal, S ;
Jermiin, LS ;
Schulte, GK ;
Danley, DE ;
Hoth, LR ;
Griffor, MC ;
Kamath, AV ;
Rosner, MH ;
Chrunyk, BA ;
Perregaux, DE ;
Gabel, CA ;
Geoghegan, KF ;
Pandit, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24798-24806