MUC genes are differently expressed during onset,and maintenance of inflammation in dextran sodium sulfate-treated mice

被引:76
作者
Hoebler, C
Gaudier, E
De Coppet, P
Rival, M
Cherbut, C
机构
[1] Inst Rech Agron, Lab Fonct Digest & Nutr Humaine, F-44316 Nantes 3, France
[2] Unite Fonct Digest & Nutr Humaine, F-44316 Nantes 3, France
关键词
mucin; Muc gene; trefoil peptide; dextran sodium sulfate; inflammation; colon;
D O I
10.1007/s10620-006-3142-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colonic mucosal protection is provided by mucous gel, mainly composed of secreted (Muc2) and membrane-bound (Muc1, Muc3, Muc4) mucins. Our aim was to determine the expression profile of secreted and membrane-bound mucins in experimental dextran sulfate sodium (DSS)-induced colitis. Acute colitis was induced in Balb/C mice by oral administration of 1.0% DSS (5 days) and chronic colitis was maintained by subsequent 0.15% DSS treatment (28 days). Clinical symptoms (mortality, weight gain), stool scores, and MPO activity confirmed the inflammatory state in the two phases of colitis. Muc2 gene expression was not modified by colitis, whereas Muc3 gene expression was increased (x2) only in the cecum and the distal colon of mice after acute colitis. Muc1 and Muc4 mRNA levels were more significantly increased in the cecum (x 8-10) than in colonic segments (x4) after acute colitis. TFF3 involved ill mucosal repair was Up-regulated during colitis induction. These results indicate that Muc and TFF3 genes are regulated early in inflammation and suggest that their mRNA levels could be used as early markers of inflammation.
引用
收藏
页码:381 / 389
页数:9
相关论文
共 30 条
[1]
Abnormalities in mucin gene expression in Crohn's disease [J].
Buisine, MP ;
Desreumaux, P ;
Debailleul, V ;
Gambiez, L ;
Geboes, K ;
Ectors, N ;
Delescaut, MP ;
Degand, P ;
Aubert, JP ;
Colombel, JF ;
Porchet, N .
INFLAMMATORY BOWEL DISEASES, 1999, 5 (01) :24-32
[2]
Mucin gene expression in intestinal epithelial cells in Crohn's disease [J].
Buisine, MP ;
Desreumaux, P ;
Leteurtre, E ;
Copin, MC ;
Colombel, JF ;
Porchet, N ;
Aubert, JP .
GUT, 2001, 49 (04) :544-551
[3]
EXPERIMENTAL COLITIS INDUCED BY DEXTRAN SULFATE IN NORMAL AND GERM-FREE MICE [J].
BYLUNDFELLENIUS, AC ;
LANDSTROM, E ;
AXELSSON, LG ;
MIDTVEDT, T .
MICROBIAL ECOLOGY IN HEALTH AND DISEASE, 1994, 7 (04) :207-215
[4]
Cell signaling through membrane mucins [J].
Carraway, KL ;
Ramsauer, VP ;
Haq, B ;
Carraway, CAC .
BIOESSAYS, 2003, 25 (01) :66-71
[5]
COOPER HS, 1993, LAB INVEST, V69, P238
[6]
Mucins and mucosal protection in the gastrointestinal tract: new prospects for mucins in the pathology of gastrointestinal disease [J].
Corfield, AP ;
Myerscough, N ;
Longman, R ;
Sylvester, P ;
Arul, S ;
Pignatelli, M .
GUT, 2000, 47 (04) :589-594
[7]
Characterisation of acute murine dextran sodium sulphate colitis:: Cytokine profile and dose dependency [J].
Egger, B ;
Bajaj-Elliott, M ;
MacDonald, TT ;
Inglin, R ;
Eysselein, VE ;
Büchler, MW .
DIGESTION, 2000, 62 (04) :240-248
[8]
Role of mucins in inflammatory bowel disease:: important lessons from experimental models [J].
Einerhand, AWC ;
Renes, IB ;
Makkink, MK ;
van der Sluis, M ;
Büller, HA ;
Dekker, J .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2002, 14 (07) :757-765
[9]
Mucin production and composition is altered in dextran sulfate sodium-induced colitis in rats [J].
Faure, M ;
Moënnoz, D ;
Montigon, F ;
Mettraux, C ;
Mercier, S ;
Schiffrin, EJ ;
Obled, C ;
Breuillé, D ;
Boza, J .
DIGESTIVE DISEASES AND SCIENCES, 2003, 48 (07) :1366-1373
[10]
Improved myeloperoxidase assay for quantitation of neutrophil influx in a rat model of endotoxin-induced uveitis [J].
Graff, G ;
Gamache, DA ;
Brady, MT ;
Spellman, JM ;
Yanni, JM .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 1998, 39 (03) :169-178