Lactation defect in mice lacking the helix-loop-helix inhibitor Id2

EMBO J. 2000 Nov 1;19(21):5772-81. doi: 10.1093/emboj/19.21.5772.

Abstract

Id proteins are thought to be negative regulators of cell differentiation and positive regulators of cell proliferation. Mammary glands of Id2(-/-) female mice reveal severely impaired lobulo-alveolar development during pregnancy. Id2(-/-) mammary epithelia show no precocious maturation, but instead exhibit intrinsic defects in both cell proliferation and cell survival, implying that the role of Id2 in pregnant mammary epithelia is mainly stimulation of cell proliferation and support of cell viability. Expression studies of genes required for mammary gland development suggest Id2 to be a downstream or parallel factor of these genes. A decrease in the DNA binding activity of Stat5 was also observed in Id2(-/-) mammary glands at 7 days post-coitus. Our results indicate an indispensable role of Id2 in pregnant mammary glands.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division
  • Cell Survival
  • DNA-Binding Proteins / deficiency*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology
  • Female
  • Helix-Loop-Helix Motifs
  • In Situ Hybridization
  • Inhibitor of Differentiation Protein 2
  • Lactation Disorders / etiology*
  • Lactation Disorders / pathology
  • Lactation Disorders / physiopathology
  • Male
  • Mammary Glands, Animal / pathology
  • Mammary Glands, Animal / physiopathology
  • Mice
  • Mice, Knockout
  • Pregnancy
  • Repressor Proteins*
  • Transcription Factors*

Substances

  • DNA-Binding Proteins
  • Idb2 protein, mouse
  • Inhibitor of Differentiation Protein 2
  • Repressor Proteins
  • Transcription Factors