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