Defective vascularization of HIF-1alpha-null embryos is not associated with VEGF deficiency but with mesenchymal cell death

Dev Biol. 1999 May 15;209(2):254-67. doi: 10.1006/dbio.1999.9253.

Abstract

Hypoxia-inducible factor 1 (HIF-1) is a dimeric transcription factor composed of HIF-1alpha and HIF-1beta subunits that plays an essential role in mammalian O2 homeostasis. In Hif1a-/- knockout mice, complete deficiency of HIF-1alpha resulted in cardiac and vascular malformations and embryonic lethality at E10.5. Between E8. 75 and E9.25 striking vascular regression and abnormal remodeling occurred in the cephalic region concomitant with marked mesenchymal cell death. Similar vascular defects were observed in HIF-1alpha- and VEGF-deficient embryos and VEGF mRNA expression was not induced by hypoxia in Hif1a-/- embryonic stem cells. Surprisingly, Hif1a-/- embryos demonstrated increased VEGF mRNA expression compared to wild-type embryos. In tissue culture cells, VEGF mRNA expression was induced by glucose deprivation independent of HIF-1alpha, providing a mechanism for increased VEGF mRNA expression in Hif1a-/- embryos, in which absence of adequate tissue perfusion resulted in both O2 and glucose deprivation. Rather than being associated with VEGF deficiency, the vascular defects in Hif1a-/- embryos were spatially correlated with cell death, the onset of which preceded vascular regression.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis
  • Cardiovascular System / embryology*
  • Cell Death
  • Cell Hypoxia
  • Cells, Cultured
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / physiology*
  • Embryonic and Fetal Development / genetics
  • Endothelial Growth Factors / biosynthesis*
  • Endothelial Growth Factors / deficiency
  • Endothelial Growth Factors / genetics
  • Endothelium, Vascular / pathology
  • Female
  • Fetal Death / genetics
  • Gene Expression Regulation, Developmental*
  • Genes, Reporter
  • Glucose / metabolism
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Lymphokines / biosynthesis*
  • Lymphokines / deficiency
  • Lymphokines / genetics
  • Male
  • Mesoderm / pathology*
  • Mice
  • Mice, Knockout
  • Microscopy, Electron, Scanning
  • Models, Biological
  • Nuclear Proteins / genetics
  • Nuclear Proteins / physiology*
  • Oxidative Stress
  • Oxygen Consumption
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Transcription Factors*
  • Transfection
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors

Substances

  • DNA-Binding Proteins
  • Endothelial Growth Factors
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Lymphokines
  • Nuclear Proteins
  • RNA, Messenger
  • Transcription Factors
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factors
  • Glucose