Cathepsins K, L, B, X and W are differentially expressed in normal and chronically inflamed gastric mucosa

被引:45
作者
Bühling, F
Peitz, U
Krüger, S
Küster, D
Vieth, M
Gebert, I
Roessner, A
Weber, E
Malfertheiner, P
Wex, T
机构
[1] Univ Magdeburg, Dept Gastroenterol Hepatol & Infect Dis, D-39120 Magdeburg, Germany
[2] Univ Magdeburg, Inst Immunol, D-39120 Magdeburg, Germany
[3] Univ Magdeburg, Inst Pathol, D-39120 Magdeburg, Germany
[4] Univ Halle Wittenberg, Fac Med, Inst Physiol Chem, D-06097 Halle Saale, Germany
关键词
cathepsins; gastric mucosa; gastritis; GERD; H; pylori;
D O I
10.1515/BC.2004.051
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
The expression of cathepsins K, L, B, X and W was studied by quantitative RTPCR in normal and inflamed gastric mucosa (antrum, corpus, cardia). Cathepsins B, L, K and X were expressed ubiquitously. In contrast, cathepsin W was expressed at very low levels. Infection by Helicobacter pylori caused a significant induction of cathepsin X (p<0.008), whereas the other cathepsins were not or only locally affected by H. pylori infection or reflux disease. Immunohistochemistry revealed specific expression of cathepsin X (macrophages), cathepsin K (parietal cells) and cathepsin W (lymphocytes), whereas cathepsins B and L were predominantly expressed in epithelial cells.
引用
收藏
页码:439 / 445
页数:7
相关论文
共 30 条
[1]  
[Anonymous], 1995, Inflammatory Bowel Diseases, DOI [DOI 10.1002/IBD.3780010103, 10.1002/ibd.3780010103]
[2]   Expression of cathepsins B, L, S, and D by gastric epithelial cells implicates them as antigen presenting cells in local immune responses [J].
Barrera, CA ;
Ye, G ;
Espejo, R ;
Gunasena, S ;
Almanza, R ;
Leary, JF ;
Crowe, SE ;
Ernst, PB ;
Reyes, VE .
HUMAN IMMUNOLOGY, 2001, 62 (10) :1081-1091
[3]   Characterization of novel anti-cathepsin W antibodies and cellular distribution of cathepsin W in the gastrointestinal tract [J].
Buhling, F ;
Kellner, U ;
Guenther, D ;
Kahl, S ;
Brömme, D ;
Weber, E ;
Malfertheiner, P ;
Wex, T .
BIOLOGICAL CHEMISTRY, 2002, 383 (7-8) :1285-1289
[4]   Classification and grading of gastritis - The updated Sydney System [J].
Dixon, MF ;
Genta, RM ;
Yardley, JH ;
Correa, P ;
Batts, KP ;
Dahms, BB ;
Filipe, MI ;
Haggitt, RC ;
Haot, J ;
Hui, PK ;
Lechago, J ;
Lewin, K ;
Offerhaus, JA ;
Price, AB ;
Riddell, RH ;
Sipponen, P ;
Solcia, E ;
Watanabe, H .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1996, 20 (10) :1161-1181
[5]  
Dohchin A, 2000, CANCER, V89, P482, DOI 10.1002/1097-0142(20000801)89:3<482::AID-CNCR2>3.0.CO
[6]  
2-5
[7]   Opposing time trends of peptic ulcer and reflux disease [J].
El-Serag, HB ;
Sonnenberg, A .
GUT, 1998, 43 (03) :327-333
[8]   Increased levels of cathepsin B and L, urokinase-type plasminogen activator and its inhibitor type-1 as an early event in gastric carcinogenesis [J].
Farinati, F ;
Herszenyi, L ;
Plebani, M ;
Carraro, P ;
DePaoli, M ;
Cardin, R ;
Roveroni, G ;
Rugge, M ;
Nitti, D ;
Grigioni, WF ;
DErrico, A ;
Naccarato, R .
CARCINOGENESIS, 1996, 17 (12) :2581-2587
[9]   Diversity in the oesophageal phenotypic response to gastro-oesophageal reflux: immunological determinants [J].
Fitzgerald, RC ;
Onwuegbusi, BA ;
Bajaj-Elliott, M ;
Saeed, IT ;
Burnham, WR ;
Farthing, MJG .
GUT, 2002, 50 (04) :451-459
[10]   Thyroid functions of mouse cathepsins B, K, and L [J].
Friedrichs, B ;
Tepel, C ;
Reinheckel, T ;
Deussing, J ;
von Figura, K ;
Herzog, V ;
Peters, C ;
Saftig, P ;
Brix, K .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (11) :1733-1745