Glucose-induced metabolic oscillations parallel those of Ca(2+) and insulin release in clonal insulin-secreting cells. A multiwell approach to oscillatory cell behavior.

Insulin secretion from glucose-stimulated pancreatic beta-cells is oscillatory, and this is thought to result from oscillations in glucose metabolism. One of the primary metabolic stimulus-secretion coupling factors is the ATP/ADP ratio, which can oscillate as a result of oscillations in glycolysis. Using a novel multiwell culture plate system, we examined oscillations in insulin release and the ATP/ADP ratio in the clonal insulin-secreting cell lines HIT T-15 and INS-1. Insulin secretion from HIT cells grown in multiwell plates oscillated with a period of 4 min, similar to that seen previously in perifusion experiments. Oscillations in the ATP/ADP ratio in cells grown under the same conditions also occurred with a period of 4 min, as did oscillations in [Ca(2+)](i) monitored by fluorescence microscopy. In INS-1 cells oscillations in insulin secretion, the ATP/ADP ratio, and [Ca(2+)](i) were also seen, but with a shorter period of about 1.5 min. These observations of oscillations in the ATP/ADP ratio are consistent with their proposed role in driving the oscillations in [Ca(2+)](i) and insulin secretion. Furthermore, these data show that, at least in the clonal beta-cell lines, cell contact or even circulatory connection is not necessary for synchronous oscillations induced by a rise in glucose.

[1]  P. Smith,et al.  Oxygen consumption oscillates in single clonal pancreatic beta-cells (HIT). , 2000, Diabetes.

[2]  B. Fredholm,et al.  Changes in cytoplasmic ATP concentration parallels changes in ATP‐regulated K+‐channel activity in insulin‐secreting cells , 1998, FEBS letters.

[3]  J. Henquin,et al.  The K+-ATP channel-independent pathway of regulation of insulin secretion by glucose: in search of the underlying mechanism. , 1998, Diabetes.

[4]  C. Wollheim,et al.  Continuous monitoring of ATP levels in living insulin secreting cells expressing cytosolic firefly luciferase , 1998, FEBS letters.

[5]  P. Bergsten,et al.  Pulsatile insulin release from pancreatic islets with nonoscillatory elevation of cytoplasmic Ca2+. , 1997, The Journal of clinical investigation.

[6]  K. Tornheim Are Metabolic Oscillations Responsible for Normal Oscillatory Insulin Secretion? , 1997, Diabetes.

[7]  M. Prentki,et al.  Signal transduction mechanisms in nutrient-induced insulin secretion , 1997, Diabetologia.

[8]  S. Chheda,et al.  Reversible Ca2+-dependent Translocation of Protein Kinase C and Glucose-induced Insulin Release* , 1996, The Journal of Biological Chemistry.

[9]  B. Fredholm,et al.  Oscillations in KATP channel activity promote oscillations in cytoplasmic free Ca2+ concentration in the pancreatic beta cell. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[10]  J. Deeney,et al.  Temporal sequence of metabolic and ionic events in glucose-stimulated clonal pancreatic beta-cells (HIT). , 1996, The Biochemical journal.

[11]  P. Bergsten,et al.  Pulsatile insulin release from mouse islets occurs in the absence of stimulated entry of Ca2+. , 1996, The Journal of clinical investigation.

[12]  M. Prentki,et al.  Are the β-Cell Signaling Molecules Malonyl-CoA and Cystolic Long-Chain Acyl-CoA Implicated in Multiple Tissue Defects of Obesity and NIDDM? , 1996, Diabetes.

[13]  B. Corkey,et al.  Temporal patterns of changes in ATP/ADP ratio, glucose 6-phosphate and cytoplasmic free Ca2+ in glucose-stimulated pancreatic beta-cells. , 1996, The Biochemical journal.

[14]  B. Corkey,et al.  Phosphofructokinase Isozymes in Pancreatic Islets and Clonal β-Cells (INS-1) , 1995, Diabetes.

[15]  P. Berggren,et al.  Dissociation between changes in cytoplasmic free Ca2+ concentration and insulin secretion as evidenced from measurements in mouse single pancreatic islets. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[16]  J. Henquin,et al.  Possible links between glucose-induced changes in the energy state of pancreatic B cells and insulin release. Unmasking by decreasing a stable pool of adenine nucleotides in mouse islets. , 1995, The Journal of clinical investigation.

[17]  D C Bradley,et al.  OOPSEG: a data smoothing program for quantitation and isolation of random measurement error. , 1995, Computer methods and programs in biomedicine.

[18]  P. Bergsten,et al.  Synchronous oscillations of cytoplasmic Ca2+ and insulin release in glucose-stimulated pancreatic islets. , 1994, The Journal of biological chemistry.

[19]  P. Berggren,et al.  Ca2+ and pancreatic B-cell function. , 1994, Biochemical Society transactions.

[20]  K. Tornheim,et al.  Bioluminometric assay of ADP and ATP at high ATP/ADP ratios: assay of ADP after enzymatic removal of ATP. , 1993, Analytical biochemistry.

[21]  P. Gilon,et al.  Oscillations of secretion driven by oscillations of cytoplasmic Ca2+ as evidences in single pancreatic islets. , 1993, The Journal of biological chemistry.

[22]  P. Gilon,et al.  Mechanisms by which glucose can control insulin release independently from its action on adenosine triphosphate-sensitive K+ channels in mouse B cells. , 1993, The Journal of clinical investigation.

[23]  N. Berman,et al.  Sustained Pulsatile Insulin Secretion From Adenomatous Human β-Cells: Synchronous Cycling of Insulin, C-Peptide, and Proinsulin , 1991, Diabetes.

[24]  D. Tillotson,et al.  Oscillations in cytosolic free Ca2+, oxygen consumption, and insulin secretion in glucose-stimulated rat pancreatic islets. , 1991, The Journal of biological chemistry.

[25]  E. Ipp,et al.  Pulsatile Insulin Secretion in Isolated Rat Islets , 1990, Diabetes.

[26]  C. Wollheim,et al.  Single islet beta‐cell stimulation by nutrients: relationship between pyridine nucleotides, cytosolic Ca2+ and secretion. , 1990, The EMBO journal.

[27]  K. Polonsky,et al.  Abnormal patterns of insulin secretion in non-insulin-dependent diabetes mellitus. , 1988, The New England journal of medicine.

[28]  H. Najafi,et al.  Identification of Glucokinase as an Alloxan-Sensitive Glucose Sensor of the Pancreatic β-Cell , 1986, Diabetes.

[29]  P. Berggren,et al.  Stimulation of insulin release by the phorbol ester 12-O-tetradecanoylphorbol 13-acetate in the clonal cell line RINm5F despite a lowering of the free cytoplasmic Ca2+ concentration. , 1986, Biochimica et biophysica acta.

[30]  L. Rosário,et al.  Pulsatile insulin release and electrical activity from single ob/ob mouse islets of Langerhans. , 1986, Advances in experimental medicine and biology.

[31]  F. Matschinsky,et al.  Pancreatic islet glucose metabolism and regulation of insulin secretion. , 1986, Diabetes/metabolism reviews.

[32]  G. Weir,et al.  Sustained oscillations of insulin, glucagon, and somatostatin from the isolated canine pancreas during exposure to a constant glucose concentration. , 1980, The Journal of clinical investigation.

[33]  J. Lowenstein,et al.  Control of phosphofructokinase from rat skeletal muscle. Effects of fructose diphosphate, AMP, ATP, and citrate. , 1976, The Journal of biological chemistry.

[34]  J. Lowenstein,et al.  The purine nucleotide cycle. Control of phosphofructokinase and glycolytic oscillations in muscle extracts. , 1975, The Journal of biological chemistry.