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PMID: 16249450 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Is there a role for locally produced interleukin-1 in the deleterious effects of high glucose or the type 2 diabetes milieu to human pancreatic islets?

Diabetes ·Vol. 54 ·No. 11 ·2005-11-00 ·Pages 3238-44

Welsh N, Cnop M, Kharroubi I, Bugliani M, Lupi R, Marchetti P, Eizirik DL

Abstract

Different degrees of beta-cell failure and apoptosis are present in type 1 and type 2 diabetes. It has been recently suggested that high glucose-induced beta-cell apoptosis in type 2 diabetes shares a final common pathway with type 1 diabetes, involving interleukin-1beta (IL-1beta) production by beta-cells, nuclear factor-kappaB (NF-kappaB) activation, and death via Fas-FasL. The aim of this study was to test whether human islet exposure to high glucose in vitro, or to the type 2 diabetes environment in vivo, induces IL-1beta expression and consequent activation of NF-kappaB-dependent genes. Human islets were isolated from five normoglycemic organ donors. The islets were cultured for 48 h to 7 days at 5.6, 11, or 28 mmol/l glucose. For comparative purposes, islets were also exposed to IL-1beta. Gene mRNA expression levels were assessed by real-time RT-PCR in a blinded fashion. Culture of the human islets at 11 and 28 mmol/l glucose induced a four- to fivefold increase in medium insulin as compared with 5.6 mmol/l glucose, but neither IL-1beta nor IL-1 receptor antagonist (IL-1ra) expression changed. IL-1beta and IL-1ra protein release to the medium was also unchanged. Stimulated human monocytes, studied in parallel, released >50-fold more IL-1beta than the islets. There was also no glucose-induced islet Fas expression. Expression of the NF-kappaB-dependent genes IkappaB-alpha and monocyte chemoattractant protein (MCP)-1 was induced in human islets by IL-1beta but not by high glucose. In a second set of experiments, human islets were isolated from seven type 2 diabetic patients and eight control subjects. The findings on mRNA levels were essentially the same as in the in vitro experiments, namely the in vivo diabetic state did not induce IL-1beta, Fas, or MCP-1 expression in human islets, and also did not modify IL-1ra expression. The present findings suggest that high glucose in vitro, or the diabetic milieu in vivo, does not induce IL-1beta production or NF-kappaB activation in human islets. This makes it unlikely that locally produced IL-1beta is an important mediator of glucotoxicity to human islets and argues against the IL-1beta-NF-kappaB-Fas pathway as a common mediator for beta-cell death in type 1 and type 2 diabetes.

MeSH Terms
Aged Cells, Cultured Diabetes Mellitus, Type 2/metabolism Dose-Response Relationship, Drug Female Glucose/metabolism,pharmacology Humans Interleukin-1/biosynthesis,metabolism Islets of Langerhans/metabolism Male Middle Aged Time Factors
Chemicals
Interleukin-1 Glucose
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Welsh Nils
Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.
Cnop Miriam
Kharroubi Ilham
Bugliani Marco
Lupi Roberto
Marchetti Piero
Eizirik Décio L
Article Info
Journal
Diabetes
Abbr.
Diabetes
ISSN
0012-1797
Published
2005-11-00
Pages
3238-44
Language
English
Region
United States
NLM ID
0372763
Subset
IM
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