| Literature DB >> 3930327 |
I L Campbell, G H Wong, J W Schrader, L C Harrison.
Abstract
Cell surface antigens of the major histocompatibility complex (MHC) play a crucial role in the initiation of immune reactions. To investigate whether the expression of MHC antigens on pancreatic islet cells could be altered, we have cultured mouse islets in the presence of interferon-gamma (IFN-gamma) and subsequently examined the levels of MHC antigen by indirect immunofluorescence using monoclonal antibodies. IFN-gamma induced a 10-fold increase in H-2K antigen expression on islet cells, the percentage of cells with detectable H-2K expression increasing from 24% to 98%. The effects of IFN-gamma on H-2D and la antigen expression were less marked, with only a twofold increase in mean fluorescence levels, the percentage of cells with detectable levels of expression increasing from 10% to 48% and 5% to 16%, respectively. Using double-indirect immunofluorescence, it was demonstrated that IFN-gamma enhanced expression of H-2K and H-2D antigens on beta-cells. However la-positive beta-cells were undetectable in the presence or absence of IFN-gamma. The ability of IFN-gamma to induce increased expression of H-2 antigens on beta-cells may represent a mechanism for targeting immune (cytotoxic) reactions to beta-cells, e.g., in autoimmune insulitis or allograft rejection.Entities:
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Year: 1985 PMID: 3930327 DOI: 10.2337/diab.34.11.1205
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461