Exocyst sec5 regulates exocytosis of newcomer insulin granules underlying biphasic insulin secretion

PLoS One. 2013 Jul 2;8(7):e67561. doi: 10.1371/journal.pone.0067561. Print 2013.

Abstract

The exocyst complex subunit Sec5 is a downstream effector of RalA-GTPase which promotes RalA-exocyst interactions and exocyst assembly, serving to tether secretory granules to docking sites on the plasma membrane. We recently reported that RalA regulates biphasic insulin secretion in pancreatic islet β cells in part by tethering insulin secretory granules to Ca(2+) channels to assist excitosome assembly. Here, we assessed β cell exocytosis by patch clamp membrane capacitance measurement and total internal reflection fluorescence microscopy to investigate the role of Sec5 in regulating insulin secretion. Sec5 is present in human and rodent islet β cells, localized to insulin granules. Sec5 protein depletion in rat INS-1 cells inhibited depolarization-induced release of primed insulin granules from both readily-releasable pool and mobilization from the reserve pool. This reduction in insulin exocytosis was attributed mainly to reduction in recruitment and exocytosis of newcomer insulin granules that undergo minimal docking time at the plasma membrane, but which encompassed a larger portion of biphasic glucose stimulated insulin secretion. Sec5 protein knockdown had little effect on predocked granules, unless vigorously stimulated by KCl depolarization. Taken together, newcomer insulin granules in β cells are more sensitive than predocked granules to Sec5 regulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • Calcium / metabolism
  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cytoplasm / drug effects
  • Cytoplasm / metabolism
  • Exocytosis
  • Glucose / metabolism
  • Humans
  • Insulin / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / cytology
  • Insulin-Secreting Cells / drug effects
  • Insulin-Secreting Cells / metabolism*
  • Mice
  • Microscopy, Fluorescence
  • Patch-Clamp Techniques
  • Potassium Chloride / metabolism
  • Potassium Chloride / pharmacology
  • Rats
  • Rats, Wistar
  • Secretory Vesicles / metabolism*
  • Vesicular Transport Proteins / deficiency
  • Vesicular Transport Proteins / genetics*

Substances

  • EXOC2 protein, human
  • Exoc2 protein, mouse
  • Insulin
  • Vesicular Transport Proteins
  • Potassium Chloride
  • Glucose
  • Calcium