A possible role for insulin in stimulating islet β-cell replication was examined in neonatal rat pancreatic monolayer cultures. Addition of insulin to serum-free medium increased the mitotic index and stimulated dose-dependent increases in [3H]-thymidine incorporation in nuclei of islet β-cells in aldehyde-thionine-stained autoradiographs. The effects of insulin were not associated with any significant changes in glucagon or somatostatin levels in the culture media. Multiplication stimulating activity (MSA), an insulin-like growth factor, was about 100-fold more potent than insulin: 3 ng/ml MSA stimulated a half-maximal increase in thymidine labeling of β-cell (+63%, P < 0.005), whereas 300 ng/ml insulin was required for a similar effect. The maximal effects of insulin and MSA were similar, and the combination of maximal stimulatory concentrations of MSA (30 ng/ml) and insulin (3000 ng/ml) was not more effective than either substance added alone, suggesting that both peptides act on the same mechanism(s) regulating β-cell replication. Furthermore, an antibody to the insulin receptor did not prevent the stimulatory effects of either insulin or MSA on thymidine labeling of β-cells. These results demonstrate that insulin can stimulate islet β-cell replication directly, possibly through a receptor for MSA or another insulin-like growth factor.
Insulin and Multiplication Stimulating Activity (an Insulin-like Growth Factor) Stimulate Islet β-Cell Replication in Neonatal Rat Pancreatic Monolayer Cultures
Alexander Rabinovitch, Carol Quigley, Thomas Russell, Yogesh Patel, Daniel H Mintz; Insulin and Multiplication Stimulating Activity (an Insulin-like Growth Factor) Stimulate Islet β-Cell Replication in Neonatal Rat Pancreatic Monolayer Cultures. Diabetes 1 February 1982; 31 (2): 160–164. https://doi.org/10.2337/diab.31.2.160
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