Activation of stimulus-secretion coupling in pancreatic beta-cells by specific products of glucose metabolism. Evidence for privileged signaling by glycolysis

• Published in: The Journal of biological chemistry Vol. 271; no. 9; pp. 4838 - 4845
• Main Authors: Mertz, R J, Worley, J F, Spencer, B, Johnson, J H, Dukes, I D
• Format: Journal Article
• Language: English
• Published: United States 01-03-1996
• Subjects: Animals; Antimycin A - pharmacology; Calcium - metabolism; Cells, Cultured; Dichloroacetic Acid - pharmacology; Electron Transport - drug effects; Glucose - metabolism; Glucose - pharmacology; Glycolysis; Insulin - metabolism; Insulin Secretion; Islets of Langerhans - drug effects; Islets of Langerhans - physiology; Kinetics; Mice; Mice, Inbred C57BL; Mitochondria - drug effects; Mitochondria - metabolism; Oxidative Phosphorylation - drug effects; Pyruvates - metabolism; Pyruvates - pharmacology; Rotenone - pharmacology; Signal Transduction - drug effects; Signal Transduction - physiology; Time Factors; Uncoupling Agents - pharmacology
• ISSN: 0021-9258
• DOI: 10.1074/jbc.271.9.4838

The energy requirements of most cells supplied with glucose are fulfilled by glycolytic and oxidative metabolism, yielding ATP. In pancreatic beta-cells, a rise in cytosolic ATP is also a critical signaling event, coupling closure of ATP-sensitive K+ channels (KATP) to insulin secretion via depolarization-driven increases in intracellular Ca2+ ([Ca2+]i). We report that glycolytic but not Krebs cycle metabolism of glucose is critically involved in this signaling process. While inhibitors of glycolysis suppressed glucose-stimulated insulin secretion, blockers of pyruvate transport or Krebs cycle enzymes were without effect. While pyruvate was metabolized in islets to the same extent as glucose, it produced no stimulation of insulin secretion and did not block KATP. A membrane-permeant analog, methyl pyruvate, however, produced a block of KATP, a sustained rise in [Ca2+]i, and an increase in insulin secretion 6-fold the magnitude of that induced by glucose. These results indicate that ATP derived from mitochondrial pyruvate metabolism does not substantially contribute to the regulation of KATP responses to a glucose challenge, supporting the notion of subcompartmentation of ATP within the beta-cell. Supranormal stimulation of the Krebs cycle by methyl pyruvate can, however, overwhelm intracellular partitioning of ATP and thereby drive insulin secretion.