Specific monoclonal antibodies against the surface of rat islet beta cells

• Published in: Cell biology international 2002-01, Vol.26 (9), p.817-828
• Main Authors: Konidaris, Constantinos, Simonson, Will, Michelsen, Birgitte, Papadopoulos, George K
• Format: Article
• Language: English
• Subjects: Animals; Animals, Newborn; Antibodies, Monoclonal - immunology; Antibody Specificity; Antigens, Surface - immunology; Antigens, Surface - isolation & purification; Autoantigens - immunology; Flow Cytometry; Fluorescent Antibody Technique; Insulinoma; Islets of Langerhans - immunology; Membrane Proteins - immunology; Membrane Proteins - isolation & purification; Pancreatic Neoplasms; Precipitin Tests; Rats; Tumor Cells, Cultured
• ISSN: 1065-6995
• DOI: 10.1016/S1065-6995(02)90952-2

Type 1 diabetes arises from the autoimmune destruction of islet beta cells, with the participation of both arms of the immune system. To better characterize the beta cell membrane, we have raised monoclonal antibodies to the surface of the INS-1 insulinoma cell line. Twenty-two such antibodies were produced, 21 of the IgG class, all reactive to different cell membrane proteins from INS-1 and neonatal islet cells, yielding identical electrophoresis patterns, with molecular weights mainly between 45 and 60 kD. We have focused on three such antibodies that recognize different protein targets, and are specific for islet beta cells. The target protein of antibody AA4, also found on monkey islets, is expressed at significantly higher levels on beta cells (55.8 vs 30.6% of cells, plus 3-4 fold increase in average fluorescence intensity per cell) when neonatal rat islet cells are incubated with high (16 mM vs 3mM) glucose concentrations. Further identification of the target antigens is in progress and is expected to shed more light on the properties of beta cell membrane proteins, and their probable participation in various disease processes.