Targeted disruption of Gb3/CD77 synthase gene resulted in the complete deletion of globo-series glycosphingolipids and loss of sensitivity to verotoxins

J Biol Chem. 2006 Apr 14;281(15):10230-5. doi: 10.1074/jbc.M600057200. Epub 2006 Feb 13.

Abstract

To examine whether globotriaosylceramide (Gb3/CD77) is a receptor for verotoxins (VTs) in vivo, sensitivity of Gb3/CD77 synthase null mutant mice to VT-2 and VT-1 was analyzed. Although wild-type mice died after administration of 0.02 microg of VT-2 or 1.0 microg of VT-1, the mutant mice showed no reaction to doses as much as 100 times that administered to wild types. Expression analysis of Gb3/CD77 in mouse tissues with antibody revealed that low, but definite, levels of Gb3/CD77 were expressed in the microvascular endothelial cells of the brain cortex and pia mater and in renal tubular capillaries. Corresponding to the Gb3/CD77 expression, tissue damage with edema, congestion, and cytopathic changes was observed, indicating that Gb3/CD77 (and its derivatives) exclusively function as a receptor for VTs in vivo. The lethal kinetics were similar regardless of lipopolysaccharide elimination in VT preparation, suggesting that basal Gb3/CD77 levels are sufficient for lethal effects of VTs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Blotting, Southern
  • Brain / metabolism
  • Chromatography, Thin Layer
  • Cytokines / metabolism
  • Escherichia coli / pathogenicity
  • Female
  • Galactosyltransferases / metabolism
  • Galactosyltransferases / physiology*
  • Gene Deletion*
  • Gene Expression Regulation
  • Gene Expression Regulation, Enzymologic*
  • Genetic Vectors
  • Glycolipids / metabolism
  • Glycosphingolipids / chemistry*
  • Immunohistochemistry
  • Inflammation
  • Interleukin-1 / metabolism
  • Kidney / metabolism
  • Kidney Tubules / metabolism
  • Kinetics
  • Lipopolysaccharides / chemistry
  • Lipopolysaccharides / metabolism
  • Lymphocytes / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Microcirculation
  • Models, Genetic
  • Mutation
  • Recombination, Genetic
  • Reverse Transcriptase Polymerase Chain Reaction
  • Shiga Toxins / chemistry*
  • Time Factors
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Cytokines
  • Glycolipids
  • Glycosphingolipids
  • Interleukin-1
  • Lipopolysaccharides
  • Shiga Toxins
  • Tumor Necrosis Factor-alpha
  • Galactosyltransferases
  • UDP-galactose-lactosylceramide alpha 1-4-galactosyltransferase