Traversal of Candida albicans across human blood-brain barrier in vitro

被引:110
作者
Jong, AY
Stins, MF
Huang, SH
Chen, SHM
Kim, KS
机构
[1] Childrens Hosp Los Angeles, Div Hematol Oncol, Los Angeles, CA 90027 USA
[2] Childrens Hosp Los Angeles, Div Infect Dis, Los Angeles, CA 90027 USA
关键词
D O I
10.1128/IAI.69.7.4536-4544.2001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Candida albicans is an opportunistic pathogen, which primarily affects neonates and immunocompromised individuals. The pathogen can invade the central nervous system, resulting in meningitis. At present, the pathogenesis of C, albicans meningitis is unclear. We used an in vitro model of the human blood-brain barrier to investigate the interaction(s) of C, albicans with human brain microvascular endothelial cells (BMEC), Binding of C, albicans to human BMEC was time and inoculum dependent. Invasion of C. albicans into human BMEC was demonstrated by using an enzyme-linked immunosorbent assay based on fluorescent staining of C, albicans with calcoflour, In contrast, avirulent Candida mutant strains and nonpathogenic yeast Saccharomyces cerevisiae were not able to bind and invade human BMEC, Morphological studies revealed that on association with human BMEC, C. albicans formed germ tubes and was able to bud intracellularly. Transmission electron microscopy showed various stages of C, albicans interactions with human BMEC, e,g,, pseudopod-like structures on human BMEC membrane and intracellular vacuole-like structures retaining C, albicans, Of interest, C. albicans was able to bud and develop pseudohyphae inside human BMEC without apparent morphological changes of the host cells. In addition, C. albicans penetrates through human BMEC monolayers without a detectable change in transendothelial electrical resistance and inulin permeability. This is the first demonstration that C, albicans is able to adhere, invade, and transcytose across human BMEC without affecting monolayer integrity. A complete understanding of the interaction(s) of C. albicans with human BMEC should contribute to the understanding of the pathogenic mechanism(s) of C, albicans meningitis.
引用
收藏
页码:4536 / 4544
页数:9
相关论文
共 49 条
[1]
COS1, a two-component histidine kinase that is involved in hyphal development in the opportunistic pathogen Candida albicans [J].
Alex, LA ;
Korch, C ;
Selitrennikoff, CP ;
Simon, MI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (12) :7069-7073
[2]
Role of the mitogen-activated protein kinase hog1p in morphogenesis and virulence of Candida albicans [J].
Alonso-Monge, R ;
Navarro-García, F ;
Molero, G ;
Diez-Orejas, R ;
Gustin, M ;
Pla, J ;
Sánchez, M ;
Nombela, C .
JOURNAL OF BACTERIOLOGY, 1999, 181 (10) :3058-3068
[3]
Citrobacter freundii invades and replicates in human brain microvascular endothelial cells [J].
Badger, JL ;
Stins, MF ;
Kim, KS .
INFECTION AND IMMUNITY, 1999, 67 (08) :4208-4215
[4]
INDUCTION OF MEMBRANE RUFFLING AND FLUID-PHASE PINOCYTOSIS IN QUIESCENT FIBROBLASTS BY RAS PROTEINS [J].
BARSAGI, D ;
FERAMISCO, JR .
SCIENCE, 1986, 233 (4768) :1061-1068
[5]
BORGVONZEPELIN M, 1995, MYCOSES, V38, P339, DOI 10.1111/j.1439-0507.1995.tb00062.x
[6]
Control of filament formation in Candida albicans by the transcriptional repressor TUP1 [J].
Braun, BR ;
Johnson, AD .
SCIENCE, 1997, 277 (5322) :105-109
[7]
Transcytosis of protein through the mammalian cerebral epithelium and endothelium .3. Receptor-mediated transcytosis through the blood-brain barrier of blood-borne transferrin and antibody against the transferrin receptor [J].
Broadwell, RD ;
BakerCairns, BJ ;
Friden, PM ;
Oliver, C ;
Villegas, JC .
EXPERIMENTAL NEUROLOGY, 1996, 142 (01) :47-65
[8]
Defective hyphal development and avirulence caused by a deletion of the SSK1 response regulator gene in Candida albicans [J].
Calera, JA ;
Zhao, XJ ;
Calderone, R .
INFECTION AND IMMUNITY, 2000, 68 (02) :518-525
[9]
Avirulence of Candida albicans CaHK1 mutants in a murine model of hematogenously disseminated candidiasis [J].
Calera, JA ;
Zhao, XJ ;
De Bernardis, F ;
Sheridan, M ;
Calderone, R .
INFECTION AND IMMUNITY, 1999, 67 (08) :4280-4284
[10]
Cell wall and secreted proteins of Candida albicans:: Identification, function, and expression [J].
Chaffin, WL ;
López-Ribot, JL ;
Casanova, M ;
Gozalbo, D ;
Martinez, JP .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (01) :130-+