1. The Cryptococcus neoformans cap10 and cap59 mutant strains, affected in glucuronoxylomannan synthesis, differentially activate human dendritic cells.
- Author
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Grijpstra J, Tefsen B, van Die I, and de Cock H
- Subjects
- B7-1 Antigen metabolism, B7-2 Antigen metabolism, Cell Differentiation immunology, Cells, Cultured, Cryptococcus neoformans genetics, Cryptococcus neoformans pathogenicity, Culture Media, Conditioned, Cytokines metabolism, Flow Cytometry, Fungal Proteins genetics, Fungal Proteins metabolism, Humans, Immunohistochemistry, Polysaccharides biosynthesis, Cryptococcus neoformans immunology, Dendritic Cells immunology, Fungal Proteins immunology, Polysaccharides immunology
- Abstract
The human pathogen Cryptococcus neoformans causes meningo-encephalitis. The polysaccharide capsule is one of the main virulence factors and consists of two distinct polysaccharides: glucuronoxylomannan and galactoxylomannan. The presence of this polysaccharide capsule was previously shown to interfere with maturation of human dendritic cells (DCs), possibly by shielding cell-wall components from interacting with these host immune cells. Here we show that two mutant strains of C. neoformans, both lacking a visible capsule due to a defect in glucuronoxylomannan synthesis, differentially activate human monocyte-derived DCs. Cells from a cap59 mutant, but not of a cap10 mutant strain, induce maturation of DCs as indicated by an increase in the expression of the costimulatory molecules CD80 and CD86, and production of the cytokines interleukin (IL)-10, IL-12p40 and tumor necrosis factor alpha. Interestingly, cap59 mutant cells reassociated with a concentrated culture medium of wild-type C. neoformans had lost their capacity to induce DC maturation. Summarizing, our data suggest that glucuronoxylomannan confers properties to the capsule that protect the fungus against activation of DCs; however, the presence of intact glucuronoxylomannan is not an absolute requirement to prevent activation of DCs.
- Published
- 2009
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