Atherosclerosis, inflammation and lipoprotein glomerulopathy in kidneys of apoE-/-/LDL-/- double knockout mice

BMC Nephrol. 2010 Aug 20:11:18. doi: 10.1186/1471-2369-11-18.

Abstract

Background: The apoE-/-/LDL-/- double knockout mice are bearing considerable structural homology to human atherosclerosis. We hypothesized, that advanced lesion formation in the renal artery is associated with kidney alterations in these mice.

Methods: Kidneys from apoE-/-/LDL-/- double knockout mice at the age of 80 weeks (n = 6) and C57/BL control mice (n = 5) were infused with Microfil, harvested and scanned with micro-CT (12 mum cubic voxels) and Nano-CT (900 nm cubic voxels). We quantitated the total vascular volume using micro-CT. Number and cross-sectional area (microm2) of glomeruli were measured using histology.

Results: At the age of 80 weeks, the renal total vascular volume fraction decreased significantly (p < 0.001) compared to controls. Moreover, the renal artery showed advanced atherosclerotic lesions with adventitial Vasa vasorum neovascularization. Perivascular inflammation was present in kidneys of apoE-/-/LDL-/- double knockout mice, predominantly involved are plasma cells and leucocytes. Glomeruli cross-sectional area (9959 +/- 1083 microm2) and number (24.8 +/- 4.5) increased in apoE-/-/LDL-/- double knockout mice compared to controls (3533 +/- 398 microm2; 17.6 +/- 3, respectively), whereas 41% of the total number of glomeruli showed evidence for lipoprotein associated glomerulopathy (LPG). Moreover, immunohistochemistry demonstrated capillary aneurysms of the glomeruli filled with factor 8 containing emboli.

Conclusion: The reduced intra-renal total vascular volume is associated with systemic atherosclerosis and glomeruli alterations in the apoE-/-/LDL-/- double knockout mouse model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apolipoproteins E / deficiency*
  • Apolipoproteins E / genetics
  • Atherosclerosis / genetics*
  • Atherosclerosis / pathology
  • Disease Models, Animal
  • Glomerulonephritis / genetics*
  • Glomerulonephritis / pathology
  • Imaging, Three-Dimensional
  • Kidney Glomerulus / ultrastructure
  • Leukocytes / pathology
  • Lipoproteins / metabolism*
  • Lipoproteins, LDL / deficiency*
  • Lipoproteins, LDL / genetics
  • Male
  • Mice
  • Mice, Knockout
  • Nanotechnology
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / pathology
  • Plasma Cells / pathology
  • Renal Artery / pathology*
  • Tomography, X-Ray Computed / methods
  • Vasa Vasorum / pathology

Substances

  • Apolipoproteins E
  • Lipoproteins
  • Lipoproteins, LDL