Increased expression of HIF-1alpha, VEGF-A and its receptors, MMP-2, TIMP-1, and ADAMTS-1 at the venous stenosis of arteriovenous fistula in a mouse model with renal insufficiency

J Vasc Interv Radiol. 2010 Aug;21(8):1255-61. doi: 10.1016/j.jvir.2010.02.043. Epub 2010 Jul 3.

Abstract

Purpose: A mouse model of renal insufficiency with arteriovenous fistula (AVF) and venous stenosis was created. The authors tested the hypothesis that there is increased gene expression of hypoxia-inducible factor-1 alpha (HIF-1alpha); vascular endothelial growth factor-A (VEGF-A) and its receptors (VEGFR-1, -2); matrix metalloproteinase-2 (MMP-2), -9 (MMP-9); tissue inhibitor of metalloproteinase-1, -2 (TIMP-1, -2); and a disintegrin and metalloproteinase thrombospondin-1 (ADAMTS-1) at the venous stenosis.

Materials and methods: Nineteen male C57BL/6 mice underwent a left nephrectomy and a surgical occlusion of the right upper pole to induce renal function characterized in eight animals. Twenty eight days later, an AVF (n = 11) was created from the right carotid artery to ipsilateral jugular vein, and the mice were killed at day 7 (n = 4) and day 14 (n = 4). The outflow and control veins were removed for gene expression. Three mice were killed at day 28 for histologic analysis.

Results: The mean serum blood urea nitrogen level remained significantly elevated for 8 weeks when compared with baseline (P < .05). By day seven, there was a significant increase in the expression of HIF-1alpha, VEGF-A, VEGFR-1, VEGFR-2, MMP-2, TIMP-1, and ADAMTS-1 at the outflow vein, with HIF-1alpha and TIMP-1 levels significantly elevated at day 14 (P < .05). By day 28, the venous stenosis was characterized by a thickened vein wall and neointima.

Conclusions: A mouse model of renal insufficiency with AVF was developed that had increased expression of HIF-1alpha, VEGF-A, VEGFR-1, VEGFR-2, MMP-2, TIMP-1, and ADAMTS-1 at the outflow vein with venous stenosis by day 28.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • ADAM Proteins / genetics*
  • ADAMTS1 Protein
  • Animals
  • Arteriovenous Shunt, Surgical / adverse effects*
  • Blood Urea Nitrogen
  • Carotid Arteries / surgery
  • Constriction, Pathologic
  • Disease Models, Animal
  • Gene Expression Regulation
  • Graft Occlusion, Vascular / enzymology
  • Graft Occlusion, Vascular / etiology
  • Graft Occlusion, Vascular / genetics*
  • Graft Occlusion, Vascular / pathology
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics*
  • Jugular Veins / enzymology*
  • Jugular Veins / pathology
  • Jugular Veins / surgery
  • Male
  • Matrix Metalloproteinase 2 / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Nephrectomy
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Renal Insufficiency / surgery*
  • Time Factors
  • Tissue Inhibitor of Metalloproteinase-1 / genetics*
  • Vascular Endothelial Growth Factor A / genetics*
  • Vascular Endothelial Growth Factor Receptor-1 / genetics*
  • Vascular Endothelial Growth Factor Receptor-2 / genetics*

Substances

  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • RNA, Messenger
  • Tissue Inhibitor of Metalloproteinase-1
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, mouse
  • Flt1 protein, mouse
  • Vascular Endothelial Growth Factor Receptor-1
  • Vascular Endothelial Growth Factor Receptor-2
  • ADAM Proteins
  • ADAMTS1 Protein
  • Adamts1 protein, mouse
  • Matrix Metalloproteinase 2
  • Mmp2 protein, mouse