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Infection and Immunity, September 2000, p. 5225-5233, Vol. 68, No. 9
Laboratoire
d'Anatomie-Pathologique,1 INSERM
364,2 INSERM
452,3 and INSERM
526,4 IFR 50, Faculté de
Médecine, 06107 Nice Cedex 01, France
Received 13 April 2000/Returned for modification 30 May
2000/Accepted 15 June 2000
Helicobacter pylori infection can induce
polymorphonuclear leukocyte (PMNL) infiltration of the gastric mucosa,
which characterizes acute chronic gastritis. The mechanisms underlying
this process are poorly documented. The lack of an in vitro model has
considerably impaired the study of transepithelial migration of PMNL
induced by H. pylori. In the present work, we used
confluent polarized monolayers of the human intestinal cell line T84
grown on permeable filters to analyze the epithelial PMNL response
induced by broth culture filtrates (BCFs) and bacterial suspensions
from different strains of H. pylori. We have evaluated the
role of the vacuolating cytotoxin VacA and of the cag
pathogenicity island (PAI) of H. pylori in PMNL migration
via their effects on T84 epithelial cells. We noted no difference in
the rates of PMNL transepithelial migration after epithelial
preincubation with bacterial suspensions or with BCFs of VacA-negative
or VacA-positive H. pylori strains. In contrast, PMNL
transepithelial migration was induced after incubation of the T84 cells
with cag PAI-positive and cagE-positive
H. pylori strains. Finally, PMNL migration was correlated
with a basolateral secretion of interleukin-8 by T84 cells, thus
creating a subepithelial chemotactic gradient for PMNL. These data
provide evidence that the vacuolating cytotoxin VacA is not involved in
PMNL transepithelial migration and that the cag PAI, with a
pivotal role for the cagE gene, provokes a transcellular
signal across T84 monolayers, inducing a subepithelial PMNL response.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Effect of Helicobacter pylori on
Polymorphonuclear Leukocyte Migration across Polarized T84 Epithelial
Cell Monolayers: Role of Vacuolating Toxin VacA and cag
Pathogenicity Island
*
Corresponding author. Mailing address: INSERM 364, Faculté de Médecine, Ave. de Valombrose, 06107 Nice Cedex
01, France. Phone: 33 4 93 37 77 07. Fax: 33 4 93 81 94 56. E-mail:
hofman{at}unice.fr.
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