Hypoplasia of endocrine and exocrine pancreas in homozygous transgenic TGF-beta1

Mol Cell Endocrinol. 2005 Jan 14;229(1-2):175-84. doi: 10.1016/j.mce.2004.08.007.

Abstract

We generated the homozygous transgenic mice with expression of the active form of TGF-beta1 by the glucagon promoter (homozygous NOD-TGF-beta1). The homozygous NOD-TGF-beta1 showed severe diabetes in 84.6%, impaired glucose tolerance, and low serum insulin levels. The final size of endocrine and whole pancreas decreased, respectively, to 6 and 34%, compared to wild-type mice. The homozygous N(2) backcross to C57BL/6 (B6-TGF-beta1) showed no diabetes, but impaired glucose tolerance and low serum insulin levels. In homozygous NOD-TGF-beta1, the expression of p15(INK4b) was induced by 3.4-fold in pancreatic islets than that in wild-type mice. Based on these, we conclude first that excessive paracrine TGF-beta1 signaling in islets results in endocrine and exocrine pancreatic hypoplasia, second that TGF-beta1decrease the final size of endocrine and exocrine pancreas presumably through regulating cell cycle via p15(INK4b) at least in endocrine pancreas, and third that hypoplastic action of TGF-beta1 of pancreatic islets is independent of the genetic background.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Cycle Proteins / metabolism
  • Crosses, Genetic
  • Cyclin-Dependent Kinase Inhibitor p15
  • Diabetes Mellitus, Type 1 / etiology
  • Female
  • Glucagon / genetics
  • Glucose Tolerance Test
  • Homozygote*
  • Hyperglycemia / etiology
  • Insulin / blood
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / pathology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred NOD
  • Mice, Transgenic
  • Pancreas, Exocrine / metabolism
  • Pancreas, Exocrine / pathology*
  • Promoter Regions, Genetic
  • Swine / genetics
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / physiology*
  • Transforming Growth Factor beta1
  • Tumor Suppressor Proteins / metabolism

Substances

  • Cdkn2b protein, mouse
  • Cell Cycle Proteins
  • Cyclin-Dependent Kinase Inhibitor p15
  • Insulin
  • Tgfb1 protein, mouse
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • Tumor Suppressor Proteins
  • Glucagon