EFFECTS OF SHIGA TOXIN 2 AND SUBTILASE ON HUMAN GLOMERULAR ENDOTHELIAL CELLS: ACTION OF AN INHIBITOR OF Gb3 RECEPTOR

AMARAL MARIA MARTA; SACERDOTI FLAVIA; REPETTO HORACIO; PATON ADRIENNE W.; PATON JAMES C.; IBARRA CRISTINA

AMSTERDAM

Congreso; 8TH INTERNATIONAL SYMPOSIUM ON SHIGA TOXIN (VEROCYTOTOXIN) PRODUCING ESCHERICHIA COLI INFECTIONS; 2012

lntroduction & Objectives: Post-diarrhea hemolytic uremic syndrome (HUS) is the most common cause of acute renal failure in children younger than S years of age in Argentina. Clinical and histological renal damage has been strongly associated with Shiga toxin type 2 (Stx2) produced by 01S7 and non-01S7 Escherichia coli {STEC). In addition, several STEC non-01S7 produce Subtilase (SubAB) that may contribute to HUS pathogenesis. Stx2 binds to the Globotriaosylceramide (Gb3) receptor located on the plasma membrane of target cells. SubAB binds the specific sialated glycans (NeuSGc), a monosaccharide identified in several food products (Paton et al. J Exp Med 200:3S, 2004). In this work we have developed primary cultures of human glomerular endothelial cells {HGEC) to evaluate the action of Stx2 and SubAB toxins. Material & Methods: HGEC were isolated from kidneys of pediatric patients undergoing nephrectomies. Glomeruli were isolated, treated with collagenase and cell cultured on 0.2 % gelatin coated flask. HGEC were confirmed asendothelial cells by positive staining for PECAM-1 and VWF. Gb3 expression was evaluated by immunofluorescence staining and TLC. HGEC were incubated with Stx2 or SubAB for 72 h and the viability was assessed by neutral red uptake. Results: Stx2 (1 pg/J.!I) and SubAB (15 pg/¡.tl) were able to cause the cytotoxic effects in the SO% of the cells (CD50).Necrosis and apoptosis of HGEC were analyzed by acridine orange-ethidium bromide staining. Stx2 (10 pg/¡.tl) caused more necrosis than apoptosis with a significant increase at 4 h: 41.0 ± 15.3 % vs. 5.2 ± 0.1 % (necrosis vs. apoptosis, p