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Capsular polysaccharides from Cryptococcus neoformans modulate production of neutrophil extracellular traps (NETs) by human neutrophils

机译:来自新型隐球菌的荚膜多糖调节人嗜中性粒细胞的嗜中性粒细胞胞外捕集器(NETs)的生产

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摘要

In the present study, we characterized the in vitro modulation of NETs (neutrophil extracellular traps) induced in human neutrophils by the opportunistic fungus Cryptococcus neoformans, evaluating the participation of capsular polysaccharides glucuronoxylomanan (GXM) and glucuronoxylomannogalactan (GXMGal) in this phenomenon. The mutant acapsular strain CAP67 and the capsular polysaccharide GXMGal induced NET production. In contrast, the wild-type strain and the major polysaccharide GXM did not induce NET release. In addition, C. neoformans and the capsular polysaccharide GXM inhibited PMA-induced NET release. Additionally, we observed that the NET-enriched supernatants induced through CAP67 yeasts showed fungicidal activity on the capsular strain, and neutrophil elastase, myeloperoxidase, collagenase and histones were the key components for the induction of NET fungicidal activity. The signaling pathways associated with NET induction through the CAP67 strain were dependent on reactive oxygen species (ROS) and peptidylarginine deiminase-4 (PAD-4). Neither polysaccharide induced ROS production however both molecules blocked the production of ROS through PMA-activated neutrophils. Taken together, the results demonstrate that C. neoformans and the capsular component GXM inhibit the production of NETs in human neutrophils. This mechanism indicates a potentially new and important modulation factor for this fungal pathogen.
机译:在本研究中,我们表征了机会性真菌新隐隐球菌在人嗜中性白细胞中诱导的NETs(嗜中性白细胞外细胞陷阱)的体外调节,评估了荚膜多糖葡糖醛酸甘露聚糖(GXM)和葡糖醛酸甘露半乳聚糖(GXMGal)的参与。突变的荚膜菌株CAP67和荚膜多糖GXMGal诱导了NET的产生。相反,野生型菌株和主要多糖GXM不诱导NET释放。此外,新孢梭菌和荚膜多糖GXM抑制了PMA诱导的NET释放。此外,我们观察到通过CAP67酵母诱导的富含NET的上清液对荚膜菌株表现出杀菌活性,中性粒细胞弹性蛋白酶,髓过氧化物酶,胶原酶和组蛋白是诱导NET杀菌活性的关键成分。通过CAP67菌株与NET诱导相关的信号传导途径取决于活性氧(ROS)和肽基精氨酸脱亚氨酶4(PAD-4)。两种多糖均未诱导ROS的产生,但是这两种分子均通过PMA活化的中性粒细胞阻断了ROS的产生。两者合计,结果表明,新孢梭菌和荚膜成分GXM抑制了人类嗜中性粒细胞中NET的产生。该机制表明该真菌病原体潜在的新的重要调控因子。

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