Selective nucleotide-release from dense-core granules in insulin-secreting cells
Open accessAbstract
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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β-cells have been genetically engineered for detection of ATP, GABA or glycine release by adenoviral infection with ATP-activated P2X2 receptors, GABAA receptors or glycine receptors.
“For example, β-cells have been genetically engineered for detection of ATP, GABA or glycine release by adenoviral infection with ATP-activated P2X2 receptors (P2X2R) (484), GABAA receptors (GABAAR) (93) or glycine receptors (GlyR) (744).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [484]
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Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men
Rorsman, P., & Ashcroft, F. M. (2018) · Physiological Reviews · doi:10.1152/physrev.00008.2017 · Cited by 793 · see citing works
Self-citationRegulation of Insulin Secretion in Human Pancreatic Islets
Rorsman, P., & Braun, M. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-030212-183754 · Cited by 599 · see citing works
Self-citation
- Authors
- Obermüller, S., Lindqvist, A., Karanauskaite, J., Galvanovskis, J., Rorsman, P., & Barg, S.
- Affiliations
- Department of Experimental Medicinal Sciences, Lund University, BMC B11, SE-221 84 Lund, Sweden
- Lund University (SE)
- Churchill Hospital (GB)
- Oregon Health & Science University (US)
- Corresponding author
- Barg, Sebastian
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2005-09-15
- Volume
- 118
- Issue
- 18
- Pages
- 4271-4282
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- OpenAlex
- W2017427555
- Cited by
- 138
- References
- 0
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 5 · 2022: 7 · 2021: 5 · 2020: 1 · 2019: 5 · 2018: 4 · 2017: 6 · 2016: 4 · 2015: 5 · 2014: 8 · 2013: 13 · 2012: 15
- FWCI
- 3.93
- Type
- journal article
- Language
- en
- Open access
- green
- urn.kb.se
- Licence
- other-oa
- Locations
- Journal of Cell Science (publishedVersion)
- PubMed (publishedVersion)
- KTH Publication Database DiVA (KTH Royal Institute of Technology) (submittedVersion, other-oa)
- Lund University Publications (Lund University) (submittedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- nucleotide release, dense core granules, insulin-secreting cells, exocytosis, ATP release, peptide hormone secretion, membrane fusion, proton release, capacitance measurement, secretory vesicles
- MeSH terms
- Insulin Secretion, Adenine Nucleotides, Adenosine Triphosphate, Amyloid, Cells, Cultured, Exocytosis, Hydrogen-Ion Concentration, Insulin, Islets of Langerhans, Membrane Potentials, Peptides, Time Factors, Transfection, Receptors, Purinergic P2, Secretory Vesicles, Islet Amyloid Polypeptide, Receptors, Purinergic P2X2
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