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Infect. Immun., 12 1996, 5085-5091, Vol 64, No. 12
S Zink, T Nass, P Rosen and JF Ernst
Migration of the fungal pathogen Candida albicans across the endothelial
cell layer is considered a prerequisite for the invasion of multiple organs
occurring in systemic candidiasis. We developed an experimental system in
which C. albicans migrates from a luminal compartment across a monolayer of
bovine aortic endothelial cells on a porous filter support to an abluminal
compartment. In this system, a C. albicans wild-type strain (ATCC 10261)
traverses the endothelial monolayer in a time-, glucose-, and cell
concentration-dependent manner. A mutant derivative unable to grow and form
hyphae (SGY-243) migrates at a reduced rate. Concomitant to
transendothelial migration, the permeability of the endothelial monolayer
for dextran diffusion markers is significantly increased. This increase in
transendothelial exchange occurs before fungal cells are detectable in the
abluminal compartment and is time, glucose, and cell concentration
dependent. A mutant strain (hOG301) unable to interact with endothelial
cells does not alter endothelial permeability. Thus, transendothelial
migration of C. albicans is able to damage the barrier function of an
endothelial monolayer. Our experimental system, which reflects key stages
of transendothelial migration of C. albicans including adherence and
passage across endothelial cells and the extracellular matrix, may be a
useful model for comparisons of transendothelial migration characteristics
of Candida strains.
Copyright © 1996, American Society for Microbiology
Migration of the fungal pathogen Candida albicans across endothelial monolayers
Diabetes-Forschungs-Institut, Heinrich-Heine-Universitat, Dusseldorf,Germany.
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