Cited by 179Pancreatic function and diabetesIon channel regulation and functionIon Transport and Channel Regulation

Na channels and two types of Ca channels in rat pancreatic B cells identified with the reverse hemolytic plaque assay.

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Hiriart, M, Matteson, D R·1988·The Journal of general physiology

Abstract

The reverse hemolytic plaque assay (RHPA) was used to study the secretory properties of single rat pancreatic B cells, and to identify insulin-secreting cells for patch-clamp experiments. In secretion studies using the RHPA, we find that the percentage of secreting B cells and the amount of insulin secreted per B cell increase as the glucose concentration is raised from 0 to 20 mM. Using the whole-cell variation of the patch-clamp technique, we find that identified B cells have three types of channels capable of carrying inward current: (a) tetrodotoxin-sensitive, voltage-dependent Na channels, which are nearly completely inactivated at -40 mV, (b) fast deactivating (FD) Ca channels, and (c) slowly deactivating (SD) Ca channels. We have shown that Na channels are functionally significant to the B cell, because tetrodotoxin partially inhibits glucose-induced insulin secretion. The properties of FD and SD Ca channels differ in several respects. FD channels deactivate at -80 mV, with a time constant of 129 microseconds, they are half-maximally activated near +15 mV, they do not inactivate during 100 ms, they conduct Ba2+ better than Ca2+, and they are very sensitive to washout during intracellular dialysis. SD channels, on the other hand, deactivate with a time constant of 2.8 ms, they are half-maximally activated near -5 mV, they inactivate rapidly, they conduct Ba2+ and Ca2+ equally well, and they are insensitive to washout.

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  • The islet's response to glucose is also due to recruitment of an increasing number of β-cells.

    “Thus, although every β-cell has the capacity to respond to glucose in a graded fashion, the islet’s response to glucose is also due to recruitment of an increasing number of β-cells (283, 402).”

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Authors
Hiriart, M., & Matteson, D. R.
Affiliations
University of Maryland, Baltimore (US)
Venue
The Journal of general physiology
Published
1988-05-01
Volume
91
Issue
5
Pages
617-639
ISSN
  • 0022-1295 (ISSN-L)
  • 1540-7748
OpenAlex
W2122610528
Cited by
179
References
0
Citations by year
2023: 2 · 2022: 1 · 2021: 3 · 2020: 1 · 2019: 1 · 2018: 5 · 2017: 1 · 2016: 1 · 2015: 2 · 2014: 8 · 2013: 5 · 2012: 1
FWCI
25.63
Type
journal article
Language
en
Open access
Locations
  • The Journal of General Physiology (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of Diabetes and Digestive and Kidney Diseases (DK-33212)
Topics
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
Keywords
pancreatic beta cells, sodium channels, calcium channels, insulin secretion, tetrodotoxin, reverse hemolytic plaque assay, patch clamp, channel inactivation, washout
MeSH terms
Insulin Secretion, Animals, Calcium, Cells, Cultured, Glucose, Hemolytic Plaque Technique, Insulin, Ion Channels, Islets of Langerhans, Male, Rats, Inbred Strains, Sodium, Rats

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