Islet Amyloid Polypeptide/Amylin in Pancreatic β-Cell Line Derived From Transgenic Mouse Insulinoma

Author:

Kanatsuka Azuma1,Makino Hideichi1,Yamaguchi Takahide1,Ohsawa Haruhiko1,Tokuyama Yoshiharu1,Saitoh Takeo1,Yamamura Ken-Ichi1,Miyazaki Jun-Ichi1,Yoshida Sho1

Affiliation:

1. Second Department of Internal Medicine, Chiba University School of Medicine Chiba Department of Disease-Related Gene Regulation Research (Sandoz), Faculty of Medicine, University of Tokyo Tokyo Institute for Medical Genetics, Kumamoto University Medical School Kumamoto, Japan

Abstract

We examined the production and secretion of IAPP in a β-cell line, MIN6, which is derived from an insulinoma obtained by targeted expression of the SV40 T-antigen gene in a transgenic mouse. RNA blot analysis revealed an abundance of IAPP and insulin II mRNA in the cells, findings comparable with those in the pancreas of a normal mouse. The presence of IAPP and insulin was confirmed immunohistochemically and by RIA. Analysis of the reverse-phase HPLC identified IAPP in cells with authentic mouse IAPP. Raising the glucose concentration from 5.6 to 25 mM failed to induce increments in IAPP and insulin II mRNAs. The cells secrete IAPP and insulin for short- and long-term incubations in response to concentration of glucose in the medium. These features resemble those of islet cells from normal animals. This β-cell line will aid in analyzing the regulation of IAPP gene expression and the mechanisms of IAPP biosynthesis and secretion.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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