Schmitt C A, Schwaeble W, Wittig B M, Meyer zum Büschenfelde K H, Dippold W G
Department of Internal Medicine, Johannes-Gutenberg-University, Mainz, Germany.
Eur J Cancer. 1999 Jan;35(1):117-24. doi: 10.1016/s0959-8049(98)00290-1.
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.
膜结合补体抑制剂CD46(膜辅因子蛋白)、CD55(衰变加速因子)和CD59(攻膜保护因子)可保护肿瘤细胞免受活化补体的溶解作用。在本研究中,共检测了14种(3种胃癌、3种结肠癌和8种胰腺癌)胃肠道肿瘤细胞系中CD46、CD55和CD59的表达情况,以及它们对γ干扰素(IFN-γ)调节作用的敏感性。通过Northern印迹杂交、逆转录-聚合酶链反应(RT-PCR)、流式细胞术和免疫染色评估IFN-γ对CD46、CD55和CD59的mRNA和蛋白表达水平的影响。在未受刺激的细胞系中,CD46和CD59转录本的表达水平相当,而CD55 mRNA的基础表达则存在异质性。使用特异性抗体在所有细胞系中均检测到了补体抑制剂蛋白。胃肠道组织标本的额外免疫组织化学染色支持了这些发现。IFN-γ在一部分细胞系中对某些转录本有微弱的诱导作用。仅在HT29细胞中观察到CD55和CD59蛋白表达上调,同时相应转录本也显著增加。我们得出结论,膜结合补体抑制剂在胃肠道肿瘤细胞中广泛表达,并且对IFN-γ的敏感性各不相同。因此,它们可能参与了胃癌、胰腺癌和结直肠癌的肿瘤逃逸机制。