Cited by 107Pancreatic function and diabetesDiabetes Treatment and ManagementDiabetes and associated disorders

Secretion of islet amyloid polypeptide in response to glucose

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Kanatsuka, A., Makino, H., Ohsawa, H., Tokuyama, Y., Yamaguchi, T., Yoshida, S., Adachi, M.·1989·FEBS Letters

Abstract

The content of isolet amyloid polypeptide (IAPP) in isolated rat pancreatic islets was determined by a radioimmunoassay. Reverse‐phase high‐performance liquid chromatography analysis revealed that a main peak of IAPP immunoreactivity in the extracts from the islets corresponded to a synthetic rat IAPP. Secretion of IAPP from the cells is regulated by the extracellular glucose concentration. Thus, IAPP may be a novel regulator for glucose homeostasis and changes in the secretion perhaps relate to insular amyloid deposits and impaired glucose tolerance in type 2 diabetes mellitus.

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Crossref · 10.1016/0014-5793(89)81527-3

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  • IAPP is co-secreted with insulin from β-cells in response to glucose stimulation at an approximate >1:20 stoichiometry.

    “IAPP is co-secreted with insulin from β-cells in response to glucose stimulation at an approximate >1:20 stoichiometry (330).”

    From Pancreatic β-Cell Electrical Activity and Insulin Secretion: Of Mice and Men (2018) · cites this paper as [330]

    The discussion (section labeled “Dilution”; page unavailable) says that IAPP was co-secreted with insulin from isolated rat pancreatic islets and that secretion was regulated by glucose. It does not state an IAPP-to-insulin stoichiometry of approximately >1:20; the Figure 3 caption describes the measurements but gives no ratio. (LLM, conf=0.84)

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Research works printed but not linked: 3

  1. Westermark, P., Wernstedt, C., Wilander, E., Hayden, D.W., O'Brien, T.D. and Johnson, K.H. (1987) Proc. Natl. Acad. Sci. USA 84, 3881-3885.
  2. Cooper, G.J.S., Wills, A.C., Claj, A., Turner, B.C., Sim, R.B. and Reid, K.B.M. (1987) Proc. Natl. Acad. Sci. USA 84, 8628-8632.
  3. Leffert, J.D., Newgard, C.B., Okamoto, H., Milburn, J.L. and Luskey, K.L. (1989) Proc. Natl. Acad. Sci. USA 87,3127-3130.

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Authors
Kanatsuka, A., Makino, H., Ohsawa, H., Tokuyama, Y., Yamaguchi, T., Yoshida, S., & Adachi, M.
Affiliations
  • Chiba University (JP)
  • JIMRO (Japan) (JP)
Corresponding author
Kanatsuka, A.
Venue
FEBS Letters
Publisher
Wiley
Published
1989-12-18
Volume
259
Issue
1
Pages
199-201
ISSN
  • 0014-5793 (ISSN-L)
  • 1873-3468
OpenAlex
W1967006902
Cited by
107
References
1
Citations by year
2026: 3 · 2022: 2 · 2021: 1 · 2020: 1 · 2018: 1 · 2017: 4 · 2016: 1 · 2015: 2 · 2014: 1 · 2013: 1 · 2012: 1
FWCI
20.30
Type
journal article
Language
en
Open access
Locations
  • FEBS Letters (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Pancreatic function and diabetes
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Diabetes and associated disorders
Keywords
amylin, glucose regulation, pancreatic islets, glucose homeostasis, type 2 diabetes, impaired glucose tolerance
MeSH terms
Amyloid, Animals, Diabetes Mellitus, Type 2, Glucose, Islets of Langerhans, Male, Radioimmunoassay, Secretory Rate, Rats, Islet Amyloid Polypeptide, In Vitro Techniques

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