Loss of Cdk4 expression causes insulin-deficient diabetes and Cdk4 activation results in beta-islet cell hyperplasia

Nat Genet. 1999 May;22(1):44-52. doi: 10.1038/8751.

Abstract

To ascertain the role of cyclin-dependent kinase 4 (Cdk4) in vivo, we have targeted the mouse Cdk4 locus by homologous recombination to generate two strains of mice, one that lacks Cdk4 expression and one that expresses a Cdk4 molecule with an activating mutation. Embryonic fibroblasts proliferate normally in the absence of Cdk4 but have a delayed S phase on re-entry into the cell cycle. Moreover, mice devoid of Cdk4 are viable, but small in size and infertile. These mice also develop insulin-deficient diabetes due to a reduction in beta-islet pancreatic cells. In contrast, mice expressing a mutant Cdk4 that cannot bind the cell-cycle inhibitor P16INK4a display pancreatic hyperplasia due to abnormal proliferation of beta-islet cells. These results establish Cdk4 as an essential regulator of specific cell types.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinases / genetics*
  • Cyclin-Dependent Kinases / metabolism
  • Diabetes Mellitus / enzymology
  • Diabetes Mellitus / genetics*
  • Diabetes Mellitus / metabolism
  • Enzyme Activation
  • Female
  • Gene Expression Regulation
  • Hyperplasia
  • Infertility, Female / genetics
  • Infertility, Male / genetics
  • Insulin / deficiency*
  • Islets of Langerhans / cytology
  • Islets of Langerhans / enzymology
  • Islets of Langerhans / pathology*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mutagenesis, Site-Directed
  • Proto-Oncogene Proteins*
  • Spermatogenesis / genetics

Substances

  • Insulin
  • Proto-Oncogene Proteins
  • Cdk4 protein, mouse
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinases