Migration of the fungal pathogen Candida albicans across the endotheli
al cell layer is considered a prerequisite for the invasion of multipl
e organs occurring in systemic candidiasis, We developed an experiment
al system in which C, albicans migrates from a luminal compartment acr
oss a monolayer of bovine aortic endothelial cells on a porous filter
support to an abluminal compartment, Ln this system, a C, albicans wil
d-type strain (ATCC 10261) traverses the endothelial monolayer in a ti
me-, glucose-, and cell concentration-dependent manner, A mutant deriv
ative unable to grow and form hyphae (SGY-243) migrates at a reduced r
ate, Concomitant to transendothelial migration, the permeability of th
e endothelial monolayer for dextran diffusion markers is significantly
increased, This increase in transendothelial exchange occurs before f
ungal cells are detectable in the abluminal compartment and is time, g
lucose, and cell concentration dependent, A mutant strain (hOG301) una
ble to interact,vith endothelial cells does not alter endothelial perm
eability, Thus, transendothelial migration of C, albicans is able to d
amage the barrier function of an endothelial monolayer, Our experiment
al system, which reflects key stages of transendothelial migration of
C, albicans including adherence and passage across endothelial cells a
nd the extracellular matrix, may be a useful model for comparisons of
transendothelial migration characteristics of Candida strains.