Abstract

Cytokine receptors from the IL-6 receptor family are comprised of ligand specific α chains and a common signalling chain, gp-130, which is also required for high affinity binding. A cDNA library generated from the β-TC3 SV40 T-antigen transformed insulinoma cell line was screened for members of this receptor family potentially relevant to both beta cell development and autoimmunity. Degenerate oligonucleotide primers to a consensus region of these receptors were used and the IL-11 receptor (α chain was identified. Despite confirmation of IL-11 receptor mRNA expression, iodinated bioactive IL-11 did not bind specifically to β-TC3 cells and gp-130-dependent cytokines did not elicit signalling events in beta cell lines. This was explained by absence of gp-130 protein or mRNA in the beta cell lines tested and in primary islets. We conclude from these resuits that the previously recognised effects of IL-6 family member cytokines on pancreatic islets must be indirect via other non-beta cells within the islet, rather than due to direct effects on beta cells themselves.

Highlights

  • The IL-6 receptor is a member of a cytokine receptor family which includes IL-11, LIF, oncostatin M (OSM), ciliary neurotrophic factor (CNTF) and cardiotrophin-1 receptors

  • Using a degenerate oligonucleotide screening strategy to identify known or novel members of the IL-6 cytokine receptor family involved in beta cell function, we have found expression of the IL-11 receptor on a beta cell line

  • We screened a pancreatic beta cell line, fl-TC3, to examine cytokine receptors which may be important during endocrine cell development

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Summary

Introduction

The IL-6 receptor is a member of a cytokine receptor family which includes IL-11, LIF, oncostatin M (OSM), ciliary neurotrophic factor (CNTF) and cardiotrophin-1 receptors. These receptors utilize a common receptor chain, gp130, for signal transduction. Whether or not cytokines of this family have an effect on pancreatic beta cell development is unknown, regenerative effects on endocrine cells have been described in IL-6 transgenic mice. Type 1 (insulin-dependent) diabetes is a T cell mediated autoimmune disease in which the pancreatic beta cells are selectively destroyed. CNTF was shown to enhance the destructive effects of IL-1 on rat islets by enhancing IL-l-mediated nitric oxide production by beta cells. CNTF was shown to enhance the destructive effects of IL-1 on rat islets by enhancing IL-l-mediated nitric oxide production by beta cells. 171 CNTF mRNA was detected in rat islet cells

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