Pancreatic β-Cells Secrete Insulin in Fast- and Slow-Release Forms
Abstract
Insulin vesicles contain a chemically rich mixture of cargo that includes ions, small molecules, and proteins. At present, it is unclear if all components of this cargo escape from the vesicle at the same rate or to the same extent during exocytosis. Here, we demonstrate through real-time imaging that individual rat and human pancreatic β-cells secrete insulin in heterogeneous forms that disperse either rapidly or slowly. In healthy pancreatic β-cells maintained in culture, most vesicles discharge insulin in its fast-release form, a form that leaves individual vesicles in a few hundred milliseconds. The fast-release form of insulin leaves vesicles as rapidly as C-peptide leaves vesicles. Healthy β-cells also secrete a slow-release form of insulin that leaves vesicles more slowly than C-peptide, over times ranging from seconds to minutes. Individual β-cells make vesicles with both forms of insulin, though not all vesicles contain both forms of insulin. In addition, we confirm that insulin vesicles store their cargo in two functionally distinct compartments: an acidic solution, or halo, and a condensed core. Thus, our results suggest two important features of the condensed core: 1) It exists in different states among the vesicles undergoing exocytosis and 2) its dissolution determines the availability of insulin during exocytosis.
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There is general agreement that many docked granules are released in response to membrane depolarization produced by sulfonylureas or high [K+]o.
“There is general agreement that many docked granules are released in response to membrane depolarization produced by sulfonylureas or high [K+]o (288, 446, 487, 617).”
From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [446]
Cites
Five stages of evolving beta-cell dysfunction during progression to diabetes
Weir, G. C., & Bonner-Weir, S. (2004) · Diabetes · doi:10.2337/diabetes.53.suppl_3.s16 · Cited by 1,126 · see citing works
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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
Biogenesis of secretory granules
Borgonovo, B., Ouwendijk, J., & Solimena, M. (2006) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2006.06.010 · Cited by 100 · see citing works
- Authors
- Michael, D. J., Ritzel, R. A., Haataja, L., & Chow, R. H.
- Affiliations
- University of Southern California (US)
- Heidelberg University (DE)
- University of California, Los Angeles (US)
- Venue
- Diabetes
- Publisher
- American Diabetes Association
- Published
- 2006-03-01
- Volume
- 55
- Issue
- 3
- Pages
- 600-607
- ISSN
- 0012-1797 (ISSN-L)
- 1939-327X
- OpenAlex
- W2122264788
- Cited by
- 98
- References
- 1
- Citations by year
- 2026: 1 · 2024: 4 · 2023: 1 · 2022: 3 · 2021: 3 · 2020: 2 · 2019: 4 · 2018: 6 · 2017: 5 · 2015: 10 · 2014: 8 · 2013: 9 · 2012: 5
- FWCI
- 8.11
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Diabetes (publishedVersion)
- PubMed (publishedVersion)
- UCLA - Biblioteca de Ciencias de la Salud (submittedVersion)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 60623, DK10181, R01DK060623, F32DK010181)
- Topics
- Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Extracellular vesicles in disease
- Keywords
- pancreatic beta cells, insulin secretion, exocytosis, C-peptide, vesicle cargo, vesicle heterogeneity, real-time imaging
- MeSH terms
- Insulin Secretion, Animals, C-Peptide, Cells, Cultured, Exocytosis, Humans, Insulin, Insulin-Secreting Cells, Rats
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