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

CA Schmitt, W Schwaeble, BM Wittig… - European journal of …, 1999 - Elsevier
CA Schmitt, W Schwaeble, BM Wittig, KHM Zum Büschenfelde, WG Dippold
European journal of cancer, 1999Elsevier
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-γ (IFN-γ). The effects of IFN-γ on
mRNA and protein expression levels of CD46, CD55 and CD59 were evaluated by Northern …
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-γ (IFN-γ). The effects of IFN-γ 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-γ 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-γ. Thus, they may be involved in tumour escape mechanisms in gastric, pancreatic and colorectal cancer.
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