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Selective nucleotide-release from dense-core granules in insulin-secreting cells
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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.
Uppsala University
Obermüller Stefanie , Department of Experimental Medicinal Sciences, Lund University, Lund
Lindqvist Anders , Department of Experimental Medicinal Sciences, Lund University, Lund
Karanauskaite Jovita , Department of Experimental Medicinal Sciences, Lund University, Lund
Galvanovskis Juris , OCDEM, Nuffield Department of Clinical Medicine, University of Oxford, Churchill Hospital, Oxford
Rorsman Patrik , Department of Experimental Medicinal Sciences, Lund University, Lund
Barg Sebastian , Department of Experimental Medicinal Sciences, Lund University, Lund
Title: Selective nucleotide-release from dense-core granules in insulin-secreting cells
Description:
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.
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