Newcomer insulin secretory granules as a highly calcium-sensitive pool

Insulin secretion is biphasic in response to a step in glucose stimulation. Recent experiments suggest that 2 different mechanisms operate during the 2 phases, with transient first-phase secretion due to exocytosis of docked granules but the second sustained phase due largely to newcomer granules. Another line of research has shown that there exist 2 pools of releasable granules with different Ca2+ sensitivities. An immediately releasable pool (IRP) is located in the vicinity of Ca2+ channels, whereas a highly Ca2+-sensitive pool (HCSP) resides mainly away from Ca2+ channels. We extend a previous model of exocytosis and insulin release by adding an HCSP and show that the inclusion of this pool naturally leads to insulin secretion mainly from newcomer granules during the second phase of secretion. We show that the model is compatible with data from single cells on the HCSP and from stimulation of islets by glucose, including L- and R-type Ca2+ channel knockouts, as well as from Syntaxin-1A-deficient cells. We also use the model to investigate the relative contribution of calcium signaling and pool depletion in controlling biphasic secretion.

[1]  P. Rorsman,et al.  Delay between Fusion Pore Opening and Peptide Release from Large Dense-Core Vesicles in Neuroendocrine Cells , 2002, Neuron.

[2]  L. Eliasson,et al.  Antibody inhibition of synaptosomal protein of 25 kDa (SNAP-25) and syntaxin 1 reduces rapid exocytosis in insulin-secreting cells. , 2006, Journal of molecular endocrinology.

[3]  Xingjun Jing,et al.  Myosin 5a Controls Insulin Granule Recruitment During Late‐Phase Secretion , 2005, Traffic.

[4]  N. Brose For Better or for Worse: Complexins Regulate SNARE Function and Vesicle Fusion , 2008, Traffic.

[5]  M. Ravier,et al.  Ca2+ microdomains and the control of insulin secretion. , 2006, Cell calcium.

[6]  P. Rorsman,et al.  Insulin granule dynamics in pancreatic beta cells , 2003, Diabetologia.

[7]  C. Wollheim,et al.  Synaptotagmins bind calcium to release insulin. , 2008, American journal of physiology. Endocrinology and metabolism.

[8]  S. Gasman,et al.  Cytoskeletal control of vesicle transport and exocytosis in chromaffin cells , 2007, Acta physiologica.

[9]  K. Gillis,et al.  Phosphomimetic Mutation of Ser-187 of SNAP-25 Increases both Syntaxin Binding and Highly Ca2+-sensitive Exocytosis , 2007, The Journal of general physiology.

[10]  G. Grodsky,et al.  Dynamics of insulin secretion by the perfused rat pancreas. , 1968, Endocrinology.

[11]  P. Halban,et al.  Glucose-stimulated insulin secretion is coupled to the interaction of actin with the t-SNARE (target membrane soluble N-ethylmaleimide-sensitive factor attachment protein receptor protein) complex. , 2003, Molecular endocrinology.

[12]  P. Halban,et al.  Regulation of pancreatic β-cell insulin secretion by actin cytoskeleton remodelling: role of gelsolin and cooperation with the MAPK signalling pathway , 2006, Journal of Cell Science.

[13]  X. Lou,et al.  Protein Kinase Activation Increases Insulin Secretion by Sensitizing the Secretory Machinery to Ca2+ , 2004, The Journal of general physiology.

[14]  D. Atlas,et al.  The voltage sensitive Lc-type Ca2+ channel is functionally coupled to the exocytotic machinery. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[15]  M. Verhage,et al.  Dissecting docking and tethering of secretory vesicles at the target membrane , 2006, The EMBO journal.

[16]  J. Lang Molecular mechanisms and regulation of insulin exocytosis as a paradigm of endocrine secretion. , 1999, European journal of biochemistry.

[17]  Zhanxiang Wang,et al.  Glucose-stimulated Cdc42 Signaling Is Essential for the Second Phase of Insulin Secretion* , 2007, Journal of Biological Chemistry.

[18]  S. Itohara,et al.  Granuphilin molecularly docks insulin granules to the fusion machinery , 2005, The Journal of cell biology.

[19]  G. Rutter,et al.  Myosin Va transports dense core secretory vesicles in pancreatic MIN6 beta-cells. , 2005, Molecular biology of the cell.

[20]  K. Gillis,et al.  A Highly Ca2+-sensitive Pool of Granules Is Regulated by Glucose and Protein Kinases in Insulin-secreting INS-1 Cells , 2004, The Journal of general physiology.

[21]  S. Nagamatsu,et al.  TIRF imaging of docking and fusion of single insulin granule motion in primary rat pancreatic beta-cells: different behaviour of granule motion between normal and Goto-Kakizaki diabetic rat beta-cells. , 2004, The Biochemical journal.

[22]  B. Edmonds,et al.  Evidence that fast exocytosis can be predominantly mediated by vesicles not docked at active zones in frog saccular hair cells , 2004, The Journal of physiology.

[23]  G. Rutter,et al.  Myosin Va Transports Dense Core Secretory Vesicles in Pancreatic MIN6 β-Cells , 2005 .

[24]  H. Meissner Electrical characteristics of the beta-cells in pancreatic islets. , 1976, Journal de physiologie.

[25]  M. Verhage,et al.  Docking of Secretory Vesicles Is Syntaxin Dependent , 2006, PloS one.

[26]  T. Südhof,et al.  Synaptotagmin-1, -2, and -9: Ca2+ Sensors for Fast Release that Specify Distinct Presynaptic Properties in Subsets of Neurons , 2007, Neuron.

[27]  O. Larsson,et al.  Syntaxin 1 interacts with the LD subtype of voltage-gated Ca2+ channels in pancreatic β cells , 1999 .

[28]  T. Südhof,et al.  Synaptotagmin-1 and -7 are functionally overlapping Ca2+ sensors for exocytosis in adrenal chromaffin cells , 2008, Proceedings of the National Academy of Sciences.

[29]  P. Meda,et al.  Munc 18‐1 and Granuphilin Collaborate During Insulin Granule Exocytosis , 2008, Traffic.

[30]  L. Eliasson,et al.  Fast exocytosis with few Ca(2+) channels in insulin-secreting mouse pancreatic B cells. , 2001, Biophysical journal.

[31]  R. Chow,et al.  Complexin II plays a positive role in Ca2+-triggered exocytosis by facilitating vesicle priming , 2008, Proceedings of the National Academy of Sciences.

[32]  Thomas C. Südhof,et al.  Munc18-1 Promotes Large Dense-Core Vesicle Docking , 2001, Neuron.

[33]  J. Henquin,et al.  Triggering and amplifying pathways of regulation of insulin secretion by glucose. , 2000, Diabetes.

[34]  J. Coorssen,et al.  Calcium-triggered Membrane Fusion Proceeds Independently of Specific Presynaptic Proteins* , 2003, Journal of Biological Chemistry.

[35]  E. Cerasi,et al.  PLASMA-INSULIN RESPONSE TO SUSTAINED HYPERGLYCEMIA INDUCED BY GLUCOSE INFUSION IN HUMAN SUBJECTS. , 1963, Lancet.

[36]  S. Yang,et al.  Synaptotagmin III isoform is compartmentalized in pancreatic beta-cells and has a functional role in exocytosis. , 2000, Diabetes.

[37]  K. Gillis,et al.  A Highly Ca 2 (cid:1) -sensitive Pool of Granules Is Regulated by Glucose and Protein Kinases in Insulin-secreting INS-1 Cells , 2004 .

[38]  Geetha Shanmugam,et al.  Stimulation of insulin release by glucose is associated with an increase in the number of docked granules in the beta-cells of rat pancreatic islets. , 2004, Diabetes.

[39]  K. Rábl,et al.  A Highly Ca2+-Sensitive Pool of Vesicles Contributes to Linearity at the Rod Photoreceptor Ribbon Synapse , 2004, Neuron.

[40]  Myriam Nenquin,et al.  In vivo and in vitro glucose-induced biphasic insulin secretion in the mouse: pattern and role of cytoplasmic Ca2+ and amplification signals in beta-cells. , 2006, Diabetes.

[41]  K. Gillis,et al.  Phosphorylation of SNAP-25 at Ser187 Mediates Enhancement of Exocytosis by a Phorbol Ester in INS-1 Cells , 2008, The Journal of Neuroscience.

[42]  T. Südhof,et al.  Membrane Fusion: Grappling with SNARE and SM Proteins , 2009, Science.

[43]  E. Neher,et al.  Protein Kinase C-Dependent Phosphorylation of Synaptosome-Associated Protein of 25 kDa at Ser187 Potentiates Vesicle Recruitment , 2002, The Journal of Neuroscience.

[44]  M. Ravier,et al.  Signals and pools underlying biphasic insulin secretion. , 2002, Diabetes.

[45]  P. Rorsman,et al.  CaV2.3 calcium channels control second-phase insulin release. , 2005, The Journal of clinical investigation.

[46]  Arthur Sherman,et al.  Identifying the targets of the amplifying pathway for insulin secretion in pancreatic beta-cells by kinetic modeling of granule exocytosis. , 2008, Biophysical journal.

[47]  E. Neher Vesicle Pools and Ca2+ Microdomains: New Tools for Understanding Their Roles in Neurotransmitter Release , 1998, Neuron.

[48]  Lena Eliasson,et al.  Novel aspects of the molecular mechanisms controlling insulin secretion , 2008, The Journal of physiology.

[49]  Mica Ohara-Imaizumi,et al.  Imaging analysis reveals mechanistic differences between first- and second-phase insulin exocytosis , 2007, The Journal of cell biology.

[50]  U. Boggi,et al.  Functional and molecular defects of pancreatic islets in human type 2 diabetes. , 2005, Diabetes.

[51]  T. Südhof,et al.  Impaired insulin secretion and glucose intolerance in synaptotagmin-7 null mutant mice , 2008, Proceedings of the National Academy of Sciences.

[52]  H. Kasai,et al.  Rab27a mediates the tight docking of insulin granules onto the plasma membrane during glucose stimulation. , 2005, The Journal of clinical investigation.

[53]  J. Gerich,et al.  Is reduced first-phase insulin release the earliest detectable abnormality in individuals destined to develop type 2 diabetes? , 2002, Diabetes.

[54]  Peng Chen,et al.  A highly Ca2+-sensitive pool of vesicles is regulated by protein kinase C in adrenal chromaffin cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[55]  Marco Capogna,et al.  A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse , 2007, Proceedings of the National Academy of Sciences.

[56]  Piero Marchetti,et al.  Phasic insulin release and metabolic regulation in type 2 diabetes. , 2002, Diabetes.

[57]  Christian Rosenmund,et al.  Supporting Online Material Materials and Methods Som Text Figs. S1 to 12 Tables S1 and S2 References and Notes Conformational Switch of Syntaxin-1 Controls Synaptic Vesicle Fusion , 2022 .

[58]  P. Rorsman,et al.  Impaired insulin secretion and glucose tolerance in β cell‐selective CaV1.2 Ca2+ channel null mice , 2003, The EMBO journal.

[59]  Bard Ermentrout,et al.  Simulating, analyzing, and animating dynamical systems - a guide to XPPAUT for researchers and students , 2002, Software, environments, tools.

[60]  T. Südhof,et al.  Unexpected Ca2+-binding properties of synaptotagmin 9. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[61]  T. Südhof,et al.  Synaptotagmins form a hierarchy of exocytotic Ca2+ sensors with distinct Ca2+ affinities , 2002, The EMBO journal.

[62]  L. Eliasson,et al.  CaM kinase II‐dependent mobilization of secretory granules underlies acetylcholine‐induced stimulation of exocytosis in mouse pancreatic B‐cells , 1999, The Journal of physiology.

[63]  藤田 卓二,et al.  Docking is not a prerequisite but a temporal constraint for fusion of secretory granules , 2009 .

[64]  S. Yang,et al.  Syntaxin 1 interacts with the L(D) subtype of voltage-gated Ca(2+) channels in pancreatic beta cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.