Human intestinal infections by Shiga toxin (Stx)-producing Escherichia coli cause hemorrhagic colitis and hemolytic uremic syndrome (HUS), which represents the main cause of acute renal failure in early childhood. In HUS, Stx released in the gut enter the blood stream and are targeted to renal endothelium. The mechanism of toxin delivery is still matter of debate, although the role of polymorphonuclear leukocytes (PMN) as Stx carrier has been indicated. The aim of this paper was to better define the interactions between Stx and human PMN. Direct and indirect flow cytometric analysis, and binding experiments with radiolabeled toxins, demonstrated that Stx bind to the surface of human mature PMN, but not to immature PMN from G-CSF-treated donors. The use of the human myeloid leukemia cells (HL-60) model for inducible cell differentiation confirmed  that the toxin binding occurs only after granulocytic differentiation. Stx binding caused a delay of the spontaneous apoptosis of PMN, as shown by the delayed appearance of apoptotic nuclei and activation of caspase 3, and by the higher number of cells negative to annexin V binding assay after 48 h. Moreover, flow cytometric analysis of mixed Stx-positive and Stx-negative PMN populations showed that the toxins were transferred from positive to negative PMN. The delayed spontaneous apoptosis and the passage of the toxic ligand from older PMN to new mature cells entering the circulation from the bone marrow may explain the previously reported persistence of Stx in the blood of children with HUS.

Interactions between Shiga toxins and human polymorphonuclear leukocytes

BRIGOTTI, MAURIZIO;CARNICELLI, DOMENICA;BARBIERI, STEFANIA;BONTADINI, ANDREA;
2008

Abstract

Human intestinal infections by Shiga toxin (Stx)-producing Escherichia coli cause hemorrhagic colitis and hemolytic uremic syndrome (HUS), which represents the main cause of acute renal failure in early childhood. In HUS, Stx released in the gut enter the blood stream and are targeted to renal endothelium. The mechanism of toxin delivery is still matter of debate, although the role of polymorphonuclear leukocytes (PMN) as Stx carrier has been indicated. The aim of this paper was to better define the interactions between Stx and human PMN. Direct and indirect flow cytometric analysis, and binding experiments with radiolabeled toxins, demonstrated that Stx bind to the surface of human mature PMN, but not to immature PMN from G-CSF-treated donors. The use of the human myeloid leukemia cells (HL-60) model for inducible cell differentiation confirmed  that the toxin binding occurs only after granulocytic differentiation. Stx binding caused a delay of the spontaneous apoptosis of PMN, as shown by the delayed appearance of apoptotic nuclei and activation of caspase 3, and by the higher number of cells negative to annexin V binding assay after 48 h. Moreover, flow cytometric analysis of mixed Stx-positive and Stx-negative PMN populations showed that the toxins were transferred from positive to negative PMN. The delayed spontaneous apoptosis and the passage of the toxic ligand from older PMN to new mature cells entering the circulation from the bone marrow may explain the previously reported persistence of Stx in the blood of children with HUS.
M. Brigotti; D. Carnicelli; E. Ravanelli; S. Barbieri; F. Ricci; A. Bontadini; A. E. Tozzi; G. Scavia; A. Caprioli; P. L. Tazzari
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/62213
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