Diabetes 53:1517-1525, 2004 © 2004 by the American Diabetes Association, Inc. Islet Secretory Defect in Insulin Receptor Substrate 1 Null Mice Is Linked With Reduced Calcium Signaling and Expression of Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA)-2b and -3
1 Research Division, Joslin Diabetes Center, and Department of Medicine, Harvard Medical School, Boston, Massachusetts
Mice with deletion of insulin receptor substrate (IRS)-1 (IRS-1 knockout [KO] mice) show mild insulin resistance and defective glucose-stimulated insulin secretion and reduced insulin synthesis. To further define the role of IRS-1 in islet function, we examined the insulin secretory defect in the knockouts using freshly isolated islets and primary ß-cells. IRS-1 KO ß-cells exhibited a significantly shorter increase in intracellular free Ca2+ concentration ([Ca2+]i) than controls when briefly stimulated with glucose or glyceraldehyde and when L-arginine was used to potentiate the stimulatory effect of glucose. These changes were paralleled by a lower number of exocytotic events in the KO ß-cells in response to the same secretagogues, indicating reduced insulin secretion. Furthermore, the normal oscillations in intracellular Ca2+ and O2 consumption after glucose stimulation were dampened in freshly isolated KO islets. Semiquantitative RT-PCR showed a dramatically reduced islet expression of sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA)-2b and -3 in the mutants. These data provide evidence that IRS-1 modulation of insulin secretion is associated with Ca2+ signaling and expression of SERCA-2b and -3 genes in pancreatic islets and provides a direct link between insulin resistance and defective insulin secretion.
Address correspondence and reprint requests to Rohit N. Kulkarni, MD, PhD, Rm. 602, Joslin Diabetes Center, One Joslin Pl., Boston MA 02215. E-mail: rohit.kulkarni{at}joslin.harvard.edu
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