Unknown

Dataset Information

0

Tumor necrosis factor alpha increases human cerebral endothelial cell Gb3 and sensitivity to Shiga toxin.


ABSTRACT: Hemolytic uremic syndrome (HUS) is associated with intestinal infection by enterohemorrhagic Escherichia coli strains that produce Shiga toxins. Globotriaosylceramide (Gb3) is the functional receptor for Shiga toxin, and tumor necrosis factor alpha (TNF-alpha) upregulates Gb3 in both human macrovascular umbilical vein endothelial cells and human microvascular brain endothelial cells. TNF-alpha treatment enhanced Shiga toxin binding and sensitivity to toxin. This upregulation was specific for Gb3 species containing normal fatty acids (NFA). Central nervous system (CNS) pathology in HUS could involve cytokine-stimulated elevation of endothelial NFA-Gb3 levels. Differential expression of Gb3 species may be a critical determinant of Shiga toxin toxicity and of CNS involvement in HUS.

SUBMITTER: Eisenhauer PB 

PROVIDER: S-EPMC98098 | biostudies-literature | 2001 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Tumor necrosis factor alpha increases human cerebral endothelial cell Gb3 and sensitivity to Shiga toxin.

Eisenhauer P B PB   Chaturvedi P P   Fine R E RE   Ritchie A J AJ   Pober J S JS   Cleary T G TG   Newburg D S DS  

Infection and immunity 20010301 3


Hemolytic uremic syndrome (HUS) is associated with intestinal infection by enterohemorrhagic Escherichia coli strains that produce Shiga toxins. Globotriaosylceramide (Gb3) is the functional receptor for Shiga toxin, and tumor necrosis factor alpha (TNF-alpha) upregulates Gb3 in both human macrovascular umbilical vein endothelial cells and human microvascular brain endothelial cells. TNF-alpha treatment enhanced Shiga toxin binding and sensitivity to toxin. This upregulation was specific for Gb3  ...[more]

Similar Datasets

| S-EPMC2258847 | biostudies-other
| S-EPMC145396 | biostudies-literature
| S-EPMC7949097 | biostudies-literature
| S-EPMC3315494 | biostudies-literature
| S-EPMC4472219 | biostudies-literature
| S-EPMC3448099 | biostudies-literature
| S-EPMC3522786 | biostudies-literature
| S-EPMC2910670 | biostudies-literature
| S-EPMC4965117 | biostudies-literature
| S-EPMC2753820 | biostudies-literature