Cited by 270Pancreatic function and diabetesCellular transport and secretionIon channel regulation and function

Exocytosis elicited by action potentials and voltage‐clamp calcium currents in individual mouse pancreatic B‐cells.

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Ammälä, C, Eliasson, L, Bokvist, K, Larsson, O, Ashcroft, F M, Rorsman, P·1993·The Journal of Physiology

Abstract

1. Measurements of membrane capacitance, as an indicator of exocytosis, and intracellular Ca2+ concentration ([Ca2+]i) were used to determine the Ca2+ dependence of secretion in single pancreatic B-cells. 2. Exocytosis was dependent on a rise in [Ca2+]i and could be evoked by activation of voltage-dependent Ca2+ currents. The threshold for depolarization-induced release was 0.5 microM [Ca2+]i. Once the [Ca2+]i threshold was exceeded, exocytosis was rapidly ( or = four action potentials. 5. Comparison of the rates of exocytosis measured in response to depolarization, mobilization of Ca2+ from intracellular stores or infusion of Ca2+ through the patch pipette suggests that [Ca2+]i at the secretory sites attains a concentration of several micromolar. This is much higher than the average [Ca2+]i detected by microfluorimetry suggesting the existence of steep spatial gradients of [Ca2+]i within the B-cell. 6. Inclusion of inhibitors of Ca2+/calmodulin-dependent protein kinase II in the intracellular solution reduced the depolarization-induced exocytotic responses suggesting this enzyme may be involved in the coupling between elevation of [Ca2+]i to stimulation of the secretory machinery. 7. The size of the unitary exocytotic event was 2 fF, corresponding to a secretory granule diameter of 250 nm. 8. Over short periods, exocytosis may be extremely fast (1 pF/s or 500 granules/s), which is much higher than the rate of endocytosis (18 fF/s or 9 granules/s). Since the latter is in bett…

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Crossref · 10.1113/jphysiol.1993.sp019966

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  • Exocytosis is triggered by depolarizations above -30 mV, is maximal around zero mV and then undergoes a secondary decrease at more positive voltages.

    “Exocytosis is triggered by depolarizations above -30 mV, is maximal around zero mV and then undergoes a secondary decrease at more positive voltages (Figure 19B).”
  • The ∩-shaped voltage dependence of exocytosis mirrors that of depolarization-evoked Ca2+ entry and the associated elevation of [Ca2+]i.

    “This ∩-shaped voltage dependence mirrors that of depolarization-evoked Ca2+ entry (see Figure 9) and the associated elevation of [Ca2+]i (14).”

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Authors
Ammälä, C., Eliasson, L., Bokvist, K., Larsson, O., Ashcroft, F. M., & Rorsman, P.
Affiliations
University of Gothenburg (SE)
Venue
The Journal of Physiology
Publisher
Wiley
Published
1993-12
Volume
472
Issue
1
Pages
665-688
ISSN
  • 0022-3751 (ISSN-L)
  • 1469-7793
OpenAlex
W2065011201
Cited by
270
References
0
Citations by year
2026: 2 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 5 · 2021: 4 · 2019: 3 · 2018: 1 · 2017: 8 · 2016: 7 · 2015: 6 · 2014: 11 · 2013: 3 · 2012: 6
FWCI
18.93
Type
journal article
Language
en
Open access
Locations
  • The Journal of Physiology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
Wellcome Trust
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 › Ion channel regulation and function
Keywords
exocytosis, pancreatic beta cells, insulin secretion, action potential, voltage-dependent calcium current, intracellular calcium concentration, calcium-dependent secretion, intracellular calcium stores, calcium/calmodulin-dependent protein kinase II, secretory granules, membrane capacitance, endocytosis, single-cell electrophysiology, mouse islets, repetitive stimulation
MeSH terms
Insulin Secretion, Action Potentials, Animals, Calcium, Electric Stimulation, Endocytosis, Exocytosis, Insulin, Intracellular Fluid, Islets of Langerhans, Isoquinolines, Piperazines, Calcium Channels, Calcium-Calmodulin-Dependent Protein Kinases, 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine, Mice, Calcium-Calmodulin-Dependent Protein Kinase Type 2, In Vitro Techniques

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