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Titan cells formation in Cryptococcus neoformans is finely tuned by environmental conditions and modulated by positive and negative genetic regulators

机译:新型隐球菌的泰坦细胞形成可通过环境条件进行微调并由正负基因调节剂调节

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摘要

The pathogenic fungus Cryptococcus neoformans exhibits morphological changes in cell size during lung infection, producing both typical size 5 to 7 μm cells and large titan cells (> 10 μm and up to 100 μm). We found and optimized in vitro conditions that produce titan cells in order to identify the ancestry of titan cells, the environmental determinants, and the key gene regulators of titan cell formation. Titan cells generated in vitro harbor the main characteristics of titan cells produced in vivo including their large cell size (>10 μm), polyploidy with a single nucleus, large vacuole, dense capsule, and thick cell wall. Here we show titan cells derived from the enlargement of progenitor cells in the population independent of yeast growth rate. Change in the incubation medium, hypoxia, nutrient starvation and low pH were the main factors that trigger titan cell formation, while quorum sensing factors like the initial inoculum concentration, pantothenic acid, and the quorum sensing peptide Qsp1p also impacted titan cell formation. Inhibition of ergosterol, protein and nucleic acid biosynthesis altered titan cell formation, as did serum, phospholipids and anti-capsular antibodies in our settings. We explored genetic factors important for titan cell formation using three approaches. Using H99-derivative strains with natural genetic differences, we showed that titan cell formation was dependent on LMP1 and SGF29 genes. By screening a gene deletion collection, we also confirmed that GPR4/5-RIM101, and CAC1 genes were required to generate titan cells and that the PKR1, TSP2, USV101 genes negatively regulated titan cell formation. Furthermore, analysis of spontaneous Pkr1 loss-of-function clinical isolates confirmed the important role of the Pkr1 protein as a negative regulator of titan cell formation. Through development of a standardized and robust in vitro assay, our results provide new insights into titan cell biogenesis with the identification of multiple important factors/pathways.
机译:致病性真菌新隐球菌在肺部感染期间表现出细胞大小的形态变化,产生典型的5至7μm细胞和大的titan细胞(> 10μm至100μm)。我们发现并优化了产生钛细胞的体外条件,以鉴定钛细胞的祖先,环境决定因素和钛细胞形成的关键基因调控因子。体外产生的泰坦细胞具有体内产生的泰坦细胞的主要特征,包括它们的大细胞尺寸(> 10μm),具有单个核的多倍体,大液泡,致密的胶囊和厚的细胞壁。在这里,我们显示了不依赖酵母生长速率而衍生自祖细胞扩大的泰坦细胞。孵化培养基的变化,缺氧,营养缺乏和低pH是触发泰坦细胞形成的主要因素,而群体感应因子(如初始接种浓度,泛酸和群体感应肽Qsp1p)也影响了泰坦细胞的形成。麦角固醇,蛋白质和核酸生物合成的抑制改变了泰坦细胞的形成,在我们的环境中血清,磷脂和抗荚膜抗体也是如此。我们使用三种方法探索了对泰坦细胞形成重要的遗传因素。使用具有自然遗传差异的H99衍生菌株,我们显示了泰坦细胞的形成依赖于LMP1和SGF29基因。通过筛选基因缺失集合,我们还确认了GPR4 / 5-RIM101和CAC1基因是生成泰坦细胞所必需的,并且PKR1,TSP2,USV101基因负调控了泰坦细胞的形成。此外,对自发性Pkr1功能丧失的临床分离株的分析证实了Pkr1蛋白作为泰坦细胞形成的负调节剂的重要作用。通过开发标准化且强大的体外测定法,我们的结果通过鉴定多种重要因素/途径,为泰坦细胞生物发生提供了新的见解。

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