Sialylated Form Of The Neural Cell Adhesion Molecule (Ncam) - A New Tool For The Identification And Sorting Of Beta-Cell Subpopulations With Different Functional Activity

To clarify the relationship between variations in beta -cell mass and pancreatic function, we investigated the possibility to analyze, quantify, and sort beta -cell subpopulations with different functional maturity. To this aim, we tested the reliability of the sialylated form of neural cell adhesion molecule (NCAM) (PSA-NCAM) as a marker of beta -cell functional activity. Islet cells isolated from adult rats were analyzed for their PSA-NCAM abundance using an anti-PSA-NCAM antibody. We found that PSA-NCAM is expressed only in beta -cells. The PSA-NCAM labeling was also studied with a fluorescence-activated cell sorter. We showed that the beta -cell population is heterogeneous for PSA-NCAM labeling. To directly determine the relationship between PSA-NCAM labeling and beta -cell activity, in vitro insulin secretion studies were performed on sorted beta -cell subpopulations using a perifusion technique. Two beta -cell subpopulations were analyzed: one that was highly labeled for PSA-NCAM and another that was poorly labeled. Insulin secretion from high PSA-NCAM-labeled beta -cells was significantly higher than that in low PSA-NCAM-labeled beta -cells. This differential expression in the beta -cell population was well correlated with differences in glucose responsiveness. PSA-NCAM seems thus suitable for use as a tool to identify beta -cell subpopulations according to their glucose responsiveness.