β-Cell proliferation after a partial pancreatectomy is independent of IRS-2 in mice

Endocrinology. 2014 May;155(5):1643-52. doi: 10.1210/en.2013-1796. Epub 2014 Feb 11.

Abstract

The glucokinase-induced up-regulation of insulin receptor substrate 2 (IRS-2) plays an important role in β-cell adaptive proliferation in response to high-fat diet-induced insulin resistance. This study aimed to investigate the role of IRS-2 in the proliferation of β-cells after a 60% partial pancreatectomy. IRS-2-deficient (IRS-2(-/-)) mice or wild-type mice were subjected to a pancreatectomy (60% partial pancreatectomy) or a sham operation (Sham). The β-cell proliferation and gene expression profiles of the islets were then assessed. Gene expression in islets from pancreatectomized and Sham C57BL/6J male mice was analyzed using a cDNA microarray analysis. To compare with β-cell proliferation induced by a high-fat diet, Gck(+/-) mice subjected to a pancreatectomy were also analyzed. The IRS-2(-/-) mice exhibited β-cell expansion and a significant increase in β-cell proliferation after the pancreatectomy, compared with the Sham group. Although glucose-stimulated insulin secretion from islets was not impaired, IRS-2(-/-) mice manifested severe hyperglycemia after the pancreatectomy. The expression levels of Aurora kinase B, Cyclin A, and Cyclin B1 in the pancreatectomized islets were also enhanced in the IRS-2(-/-) mice. A gene set enrichment analysis suggested an association between the genes that were up-regulated in the pancreatectomized islets and those involved in M phase progression in the cell cycle. β-Cell proliferation after a pancreatectomy was observed even in the Gck(+/-) mice. In conclusion, IRS-2 was not required for β-cell proliferation but might be needed for functional β-cell mass, after a pancreatectomy. A partial pancreatectomy in mice may be an attractive model for the development of new strategy for exploring the unique nature of β-cell proliferation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aurora Kinase B / biosynthesis
  • Aurora Kinase B / genetics
  • Aurora Kinase B / metabolism
  • Cell Proliferation
  • Crosses, Genetic
  • Cyclin A1 / biosynthesis
  • Cyclin A1 / genetics
  • Cyclin A1 / metabolism
  • Cyclin B1 / biosynthesis
  • Cyclin B1 / genetics
  • Cyclin B1 / metabolism
  • Diet, High-Fat / adverse effects
  • Glucokinase / genetics
  • Glucokinase / metabolism
  • Hyperglycemia / blood
  • Hyperglycemia / etiology
  • Hyperglycemia / metabolism
  • Hyperglycemia / pathology
  • Insulin / metabolism
  • Insulin Receptor Substrate Proteins / genetics
  • Insulin Receptor Substrate Proteins / metabolism*
  • Insulin Secretion
  • Insulin-Secreting Cells / metabolism
  • Insulin-Secreting Cells / pathology
  • Insulin-Secreting Cells / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Pancreatectomy / adverse effects*
  • Regeneration*
  • Signal Transduction
  • Up-Regulation

Substances

  • Ccna1 protein, mouse
  • Ccnb1 protein, mouse
  • Cyclin A1
  • Cyclin B1
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs2 protein, mouse
  • Glucokinase
  • Aurkb protein, mouse
  • Aurora Kinase B