Shiga toxin 2 and lipopolysaccharide cause monocytic THP-1 cells to release factors which activate platelet function

Fadila Guessous; Marek Marcinkiewicz; Renata Polanowska-Grabowska; Tiffany R. Keepers; Tom Obrig; Adrian R. L. Gear

doi:10.1160/TH05-02-0115

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 2005; 94(05): 1019-1027
DOI: 10.1160/TH05-02-0115

Platelets and Blood Cells

Schattauer GmbH

Shiga toxin 2 and lipopolysaccharide cause monocytic THP-1 cells to release factors which activate platelet function

Authors

Fadila Guessous

¹Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia, USA
Marek Marcinkiewicz

¹Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia, USA
Renata Polanowska-Grabowska

¹Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia, USA
Tiffany R. Keepers

²Division of Nephrology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA
Tom Obrig

²Division of Nephrology, Department of Medicine, University of Virginia School of Medicine, Charlottesville, Virginia, USA
Adrian R. L. Gear

¹Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, Virginia, USA

Abstract

Summary

Platelet and monocyte activation may contribute to hemolytic anemia, thrombocytopenia and renal failure associated with the hemolytic uremic syndrome (HUS) caused by Escherichia coli O157:H7. Since Shiga toxins (Stxs) and lipopolysaccharide (LPS) from this bacterium are implicated in the pathogenesis of HUS, we examined whether stimulation of THP-1 human monocytic cells by Shiga toxin 2 (Stx2) and LPS can lead to the activation of platelet function. We now show that Stx2 caused THP-1 cells to release the chemokines IL-8, MDC, and RANTES and that the presence of LPS further stimulated this release. IL-8 was produced in greatest amount and was an effective co-agonist for inducing platelet aggregation. Primary human monocytes also released large amounts of IL-8 in response to LPS and Stx2. Factors released by THP-1 cells exposed to Stx2 and LPS activated platelet function as evidenced by increased aggregation, serotonin secretion, P-selectin exposure and by the formation of stable platelet-monocyte aggregates. Our data therefore show that monocytes exposed to E. coli-derived Stx2 and LPS release factors which activate platelet function.

Keywords

Shiga toxin - lipopolysaccharide (LPS) - platelets - aggregation - chemokines - monocytes (THP-1) - secretion - hemolytic uremic syndrome (HUS) - IL-8 - RANTES

Full Text

References

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