Cited by 98Pancreatic function and diabetesCellular transport and secretionExtracellular vesicles in disease

Pancreatic β-Cells Secrete Insulin in Fast- and Slow-Release Forms

Michael, Darren J., Ritzel, Robert A., Haataja, Leena, Chow, Robert H.·2006·Diabetes

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.

Integrity signals

Registry

Crossref · 10.2337/diabetes.55.03.06.db05-1054

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1 of 1 references verified0 citation errors · 0 not checkable

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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).”

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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
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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