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Infect. Immun., Mar 1995, 976-983, Vol 63, No. 3
SG Filler, JN Swerdloff, C Hobbs and PM Luckett
The mechanisms of phagocytosis of Candida albicans by human vascular
endothelial cells and subsequent endothelial cell injury were examined in
vitro. Both live and killed C. albicans cells were phagocytized by
endothelial cells. This organism specifically induced endothelial cell
phagocytosis because neither Candida tropicalis nor Torulopsis glabrata was
ingested. Endothelial cell microfilaments polymerized around C. albicans as
the organisms were phagocytized. Cytochalasin D inhibited this
polymerization of microfilaments around C. albicans and blocked
phagocytosis. The blocking of actin depolymerization with phalloidin had no
effect on microfilament condensation around the organism, indicating that
the microfilaments surrounding C. albicans are formed from a pool of
G-actin. Intact microtubules were also necessary for the phagocytosis of C.
albicans, since the depolymerizing of endothelial cell microtubules with
nocodazole prevented the condensation of actin filaments around the
organisms and inhibited phagocytosis. In contrast, microtubule
depolymerization was not required for microfilament function because the
blocking of microtubule depolymerization with taxol had no effect on
microfilament condensation around C. albicans. The phagocytosis of C.
albicans was pivotal in the induction of endothelial cell damage, since the
blocking of candidal internalization significantly reduced endothelial cell
injury. Endothelial cells were not damaged by phagocytosis of dead
organisms, indicating that injury was caused by a factor associated with
viable organisms. Therefore, C. albicans is uniquely able to induce
endothelial cell phagocytosis by comparison with non-albicans species of
Candida. Furthermore, at least two components of the endothelial
cytoskeleton, microfilaments and microtubules, are necessary for the
phagocytosis of C. albicans.
Copyright © 1995, American Society for Microbiology
Penetration and damage of endothelial cells by Candida albicans
Department of Internal Medicine, UCLA School of Medicine, St. John's Cardiovascular Research Center, Harbor-UCLA Research and Education Institute, Torrance 90509.
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