Selective nucleotide-release from dense-core granules in insulin-secreting cells

J Cell Sci. 2005 Sep 15;118(Pt 18):4271-82. doi: 10.1242/jcs.02549. Epub 2005 Sep 1.

Abstract

Secretory granules of insulin-secreting cells are used to store and release peptide hormones as well as low-molecular-weight compounds such as nucleotides. Here we have compared the rate of exocytosis with the time courses of nucleotide and peptide release by a combination of capacitance measurements, electrophysiological detection of ATP release and single-granule imaging. We demonstrate that the release of nucleotides and peptides is delayed by approximately 0.1 and approximately 2 seconds with respect to membrane fusion, respectively. We further show that in up to 70% of the cases exocytosis does not result in significant release of the peptide cargo, likely because of a mechanism that leads to premature closure of the fusion pore. Release of nucleotides and protons occurred regardless of whether peptides were secreted or not. These observations suggest that insulin-secreting cells are able to use the same secretory vesicles to release small molecules either alone or together with the peptide hormone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine Nucleotides / metabolism*
  • Adenosine Triphosphate / pharmacology
  • Amyloid / metabolism
  • Cells, Cultured
  • Exocytosis / physiology
  • Hydrogen-Ion Concentration
  • Insulin / metabolism
  • Insulin Secretion
  • Islet Amyloid Polypeptide
  • Islets of Langerhans / metabolism*
  • Membrane Potentials / physiology
  • Peptides / metabolism
  • Receptors, Purinergic P2 / metabolism
  • Receptors, Purinergic P2X2
  • Secretory Vesicles / metabolism*
  • Time Factors
  • Transfection

Substances

  • Adenine Nucleotides
  • Amyloid
  • Insulin
  • Islet Amyloid Polypeptide
  • Peptides
  • Receptors, Purinergic P2
  • Receptors, Purinergic P2X2
  • Adenosine Triphosphate