Increased amounts of a high molecular weight insulin-like growth factor II (IGF-II) peptide and IGF-II messenger ribonucleic acid in pancreatic islets of diabetic Goto …

A Höög, AC Sandberg-Nordqvist… - …, 1996 - academic.oup.com
A Höög, AC Sandberg-Nordqvist, SM Abdel-Halim, C Carlsson-Skwirut, A Guenifi, M Tally…
Endocrinology, 1996academic.oup.com
Insulin-like growth factor II (IGF-II), a member of the insulin family, regulates cell growth and
differentiation. The IGF-II gene is localized close to the insulin gene in man and rat. IGF-II
peptide binds weakly to the insulin receptor and exerts insulin-like effects on the blood
glucose level. We studied IGF-II in endocrine pancreas in an animal model of noninsulin-
dependent diabetes mellitus, the Goto-Kakizaki (GK) rat. At the age of 2 months, these rats
have structural islet changes, with fibrosis and irregular configuration, so-called starfish …
Abstract
Insulin-like growth factor II (IGF-II), a member of the insulin family, regulates cell growth and differentiation. The IGF-II gene is localized close to the insulin gene in man and rat. IGF-II peptide binds weakly to the insulin receptor and exerts insulin-like effects on the blood glucose level. We studied IGF-II in endocrine pancreas in an animal model of noninsulin-dependent diabetes mellitus, the Goto-Kakizaki (GK) rat. At the age of 2 months, these rats have structural islet changes, with fibrosis and irregular configuration, so-called starfish-shaped islets. Immunohistochemical investigation revealed IGF-II immunoreactivity in the beta-cells in both GK and control rats. Pancreatic extraction, followed by size separation using gel chromatography, disclosed a high mol wt form of IGF-II in all animals, and RIA measurements revealed a considerably larger amount of the IGF-II peptide in the 2-and 6-month-old GK rats than in the 1-month GK and control rats. In situ hybridization of 3-month-old GK rats showed increased IGF-II messenger RNA expression in the starfish-shaped islets of GK rats than in the islets with normal structure in both diabetic and control animals. The reason for the increased amount of IGF-II is unclear. As the animals are diabetic before the islet changes occur, it might be a compensatory effect in response to hyperglycemia, but could also be a cause of the islet fibrosis.
Oxford University Press