Publication: The histopathology of Candida albicans
invasion in neonatal rat tissues and in the human
blood-brain barrier in culture revealed by light, scanning,
transmission and immunoelectron microscopy scanning
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Date
2006
Authors
Lossinsky, A.S. ; Jong, A. ; Fiala, M. ; Mukhtar, M. ; Buttle, K.F. ; Ingram, M.
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
The present studies examined the effects of
Candida albicans yeast and hyphal morphologies on
tissue pathologies and transmigration properties of the
fungus in two experimental models: 1) an in vivo,
neonatal rat model, and 2) a cell culture model of human
brain microvascular endothelial cells (ECs) (BMVEC).
We inoculated a hyphae-producing strain (CAI4-URA3)
and a non-hyphae-producing strain (CAI4) of C.
albicans into 4-10 day old rats and BMVEC cultures.
Animals were inoculated by intraperitonal (i.p.),
intranasal (i.n.), oral (p.o.) and intracerebral (i.c.) routes
and several tissues were examined after 24-48 hrs. Rats
inoculated i.p. with the hyphae-producing strain showed
pathology in the kidneys, liver, spleen, and other tissues
associated with inoculation tracks of the nose, and
muscle and connective tissues of the abdominal wall.
Few animals inoculated i.p., however, presented
evidence of meningitis. The non-hyphae phase yeast
produced neither tissue pathology nor meningitis.
Animals inoculated i.c. with the hyphae strain after 1
and 3 hrs expressed minimal meningitis, with an
increasing neutrophillic meningitis between 4 and 18 hrs
after inoculation. At 18 hrs after i.c. inoculation,
however, the inflammatory foci and brain pathology
were extensive and demonstrated mycelia within the
lateral ventricles associated with necrosis of adjacent
brain tissue. Neutrophillic meningitis at this time period was pronounced. BMVEC co-cultured 1-2 hrs with both
C. albicans strains showed EC phagocytosis of hyphae
and blastospores into intercellular adhesion molecule-1
(ICAM-1)-labeled caveolae suggesting a transcellular
role for ICAM-1 in the internalization process of C.
albicans.
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