Granulocyte-macrophage colony-stimulating factor responses of oral epithelial cells to Candida albicans

被引:24
作者
Dongari-Bagtzoglou, A [1 ]
Kashleva, H [1 ]
机构
[1] Univ Connecticut, Sch Dent Med, Farmington, CT 06032 USA
来源
ORAL MICROBIOLOGY AND IMMUNOLOGY | 2003年 / 18卷 / 03期
关键词
Candida albicans; epithelial cells; GM-CSF; NECROSIS-FACTOR-ALPHA; ENDOTHELIAL-CELLS; GM-CSF; PROINFLAMMATORY CYTOKINES; HIV-INFECTION; IN-VITRO; IL-6; ADHERENCE; EXPOSURE; INTERLEUKIN-6;
D O I
10.1034/j.1399-302X.2003.00061.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Candida albicans is the principal fungal species responsible for oropharyngeal candidiasis, the most frequent opportunistic infection associated with immune deficiencies. Cytokines, such as granulocyte-macrophage colony-stimulating factor (GM-CSF), are important in the generation of effective immunity to C. albicans . The purposes of this investigation were to determine whether C. albicans triggers secretion of GM-CSF by oral epithelial cells in vitro and to investigate mechanisms of host cell-fungal interactions that trigger such responses. Oral epithelial cell lines as well as primary oral mucosal epithelial cells were challenged with stationary phase viable C. albicans , added to human cell cultures at varying yeast:oral cell ratios. Yeast were allowed to germinate for up to 48 h and supernatants were analyzed for GM-CSF by ELISA. Fixed organisms, germination-deficient mutants and separation of yeast from epithelial cells using cell culture inserts were used to assess the effects of viability, germination and physical contact, respectively, on the GM-CSF responses of these cells. Two out of three cell lines and three out of six primary cultures responded to C. albicans with an increase in GM-CSF secretion. GM-CSF responses were contact-dependent, strain-dependent, required yeast viability and were optimal when the yeast germinated into hyphae.
引用
收藏
页码:165 / 170
页数:6
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