Cryptococcus neoformans capsular glucuronoxylomannan induces expression of fas ligand in macrophages

被引:75
作者
Monari, C
Pericolini, E
Bistoni, G
Casadevall, A
Kozel, TR
Vecchiarelli, A
机构
[1] Univ Perugia, Microbiol Sect, Dept Expt Med & Biochem Sci, I-06122 Perugia, Italy
[2] Univ London Imperial Coll Sci Technol & Med, London, England
[3] Albert Einstein Coll Med, Dept Med, Bronx, NY 10461 USA
[4] Univ Nevada, Dept Microbiol & Immunol, Reno, NV 89557 USA
关键词
D O I
10.4049/jimmunol.174.6.3461
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The major component of capsular material of Cryptococcus neoformans is glucuronoxylomannnan (GXM), a polysaccharide that exhibits potent immunosuppressive properties in vitro and in vivo. The results reported here show that 1) soluble purified GXM induces a prompt, long-lasting, and potent up-regulation of Fas ligand (FasL) on macrophages, 2) the up-regulation of FasL is related to induced synthesis and increased mobilization to the cellular surface, 3) this effect is largely mediated by interaction between GXM and TLR4, 4) FasL, up-regulation occurs exclusively in GXM-loaded macrophages, 5) macrophages that show up-regulation of FasL induce apoptosis of activated T cells expressing Fas and Jurkat cells that constitutively express Fas, and 6) anti-Fas Abs rescue T cells from apoptosis induced by GXM. Collectively our results reveal novel aspects of the immunoregulatory properties of GXM and suggest that this nontoxic soluble compound could be used to dampen the immune response, to promote or accelerate the death receptor, and to fix FasL expression in a TLP/ligand-dependent manner. In the present study, we delineate potential new therapeutic applications for GXM that exploit death receptors as key molecular targets in regulating cell-mediated cytotoxicity, immune homeostasis, and the immunopathology of diseases.
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页码:3461 / 3468
页数:8
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