Expression and regulation by interferon-γ of the membrane-bound complement regulators CD46 (MCP), CD55 (DAF) and CD59 in gastrointestinal tumours

被引:37
作者
Schmitt, CA
Schwaeble, W
Wittig, BM
zum Büschenfelde, KHM
Dippold, WG
机构
[1] St Vinzenz & Elisabeth Hosp, Dept Internal Med, D-55131 Mainz, Germany
[2] Univ Leicester, Dept Microbiol & Immunol, Leicester LE1 7RH, Leics, England
[3] Johannes Gutenberg Univ Mainz, Dept Internal Med, D-6500 Mainz, Germany
关键词
CD46 (MCP); CD55 (DAF); CD59 (protectin); colon cancer; complement regulators; gastric cancer; immunotherapy; interferon-gamma; pancreatic cancer;
D O I
10.1016/S0959-8049(98)00290-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The membrane-bound complement inhibitors CD46 (membrane cofactor protein), CD55 (decay-accelerating factor) and CD59 (protectin) protect tumour cells against lysis by activated complement. In this study, a total of 14 (3 gastric, 3 colonic and 8 pancreatic) gastrointestinal tumour cell lines were examined for the expression of CD46, CD55 and CD59 with respect to the regulatory efficacy of interferon-gamma (IFN-gamma). The effects of IFN-gamma on mRNA and protein expression levels of CD46, CD55 and CD59 were evaluated by Northern blot hybridisation, RT-PCR, flow cytometry and immunostaining. In unstimulated cell lines, CD46 and CD59 transcripts were expressed at comparable levels, whereas the basal expression of CD55 mRNA was heterogeneous. The complement inhibitor proteins were detected in all cell lines using specific antibodies. Additional immunohistochemical stainings of gastrointestinal tissue specimens supported these findings. IFN-gamma evoked a weak induction of certain transcripts in a subset of the cell lines. Upregulation of protein expression was only observed in HT29 cells for CD55 and CD59 and was accompanied by a marked increase of the corresponding transcripts. We conclude that membrane-bound complement inhibitors are broadly expressed in gastrointestinal tumour cells and vary in their susceptibility to IFN-gamma. Thus, they may be involved in tumour escape mechanisms in gastric, pancreatic and colorectal cancer. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:117 / 124
页数:8
相关论文
共 48 条
[1]   Interleukin 4 acts as an inducer of decay-accelerating factor gene expression in human intestinal epithelial cells [J].
Andoh, A ;
Fujiyama, Y ;
Sumiyoshi, K ;
Sakumoto, H ;
Bamba, T .
GASTROENTEROLOGY, 1996, 111 (04) :911-918
[2]  
ANDOH A, 1993, J IMMUNOL, V151, P4239
[3]   SEPARATION OF SELF FROM NON-SELF IN THE COMPLEMENT-SYSTEM [J].
ATKINSON, JP ;
FARRIES, T .
IMMUNOLOGY TODAY, 1987, 8 (7-8) :212-215
[4]   THE INFLUENCE OF TUMOR-NECROSIS-FACTOR-ALPHA, INTERLEUKIN-1-BETA AND INTERFERON-GAMMA ON THE EXPRESSION AND FUNCTION OF THE COMPLEMENT REGULATORY PROTEIN CD59 ON THE HUMAN COLONIC ADENOCARCINOMA CELL-LINE HT29 [J].
BJORGE, L ;
JENSEN, TS ;
ULVESTAD, E ;
VEDELER, CA ;
MATRE, R .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1995, 41 (04) :350-356
[5]   Characterisation of the complement-regulatory proteins decay-accelerating factor (DAF,CD55) and membrane cofactor protein (MCP,CD46) on a human colonic adenocarcinoma cell line [J].
Bjorge, L ;
Jensen, TS ;
Matre, R .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 1996, 42 (03) :185-192
[6]  
BJORGE L, 1994, EUR J IMMUNOL, V24, P1597
[7]   RELATIVE ROLES OF DECAY-ACCELERATING FACTOR, MEMBRANE COFACTOR PROTEIN, AND CD59 IN THE PROTECTION OF HUMAN ENDOTHELIAL-CELLS AGAINST COMPLEMENT-MEDIATED LYSIS [J].
BROOIMANS, RA ;
VANWIERINGEN, PAM ;
VANES, LA ;
DAHA, MR .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (12) :3135-3140
[8]   CLONING OF DECAY-ACCELERATING FACTOR SUGGESTS NOVEL USE OF SPLICING TO GENERATE 2 PROTEINS [J].
CARAS, IW ;
DAVITZ, MA ;
RHEE, L ;
WEDDELL, G ;
MARTIN, DW ;
NUSSENZWEIG, V .
NATURE, 1987, 325 (6104) :545-549
[9]   RECOMBINANT INTERFERON-GAMMA CAN INDUCE THE EXPRESSION OF HLA-DR AND HLA-DC ON DR-NEGATIVE MELANOMA-CELLS AND ENHANCE THE EXPRESSION OF HLA-ABC AND TUMOR-ASSOCIATED ANTIGENS [J].
CARREL, S ;
SCHMIDTKESSEN, A ;
GIUFFRE, L .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1985, 15 (02) :118-123
[10]   DECAY-ACCELERATING FACTOR PROTECTS HUMAN-TUMOR CELLS FROM COMPLEMENT-MEDIATED CYTO-TOXICITY INVITRO [J].
CHEUNG, NKV ;
WALTER, EI ;
SMITHMENSAH, WH ;
RATNOFF, WD ;
TYKOCINSKI, ML ;
MEDOF, ME .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (04) :1122-1128