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Characterization of Yeast Extracellular Vesicles: Evidence for the Participation of Different Pathways of Cellular Traffic in Vesicle Biogenesis

机译:酵母细胞外囊泡的表征:细胞交通不同途径参与囊泡生物合成的证据

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摘要

Background: Extracellular vesicles in yeast cells are involved in the molecular traffic across the cell wall. In yeast pathogens, these vesicles have been implicated in the transport of proteins, lipids, polysaccharide and pigments to the extracellular space. Cellular pathways required for the biogenesis of yeast extracellular vesicles are largely unknown. Methodology/Principal Findings: We characterized extracellular vesicle production in wild type (WT) and mutant strains of the model yeast Saccharomyces cerevisiae using transmission electron microscopy in combination with light scattering analysis, lipid extraction and proteomics. WT cells and mutants with defective expression of Sec4p, a secretory vesicle-associated Rab GTPase essential for Golgi-derived exocytosis, or Snf7p, which is involved in multivesicular body (MVB) formation, were analyzed in parallel. Bilayered vesicles with diameters at the 100-300 nm range were found in extracellular fractions from yeast cultures. Proteomic analysis of vesicular fractions from the cells aforementioned and additional mutants with defects in conventional secretion pathways (sec1-1, fusion of Golgi-derived exocytic vesicles with the plasma membrane; bos1-1, vesicle targeting to the Golgi complex) or MVB functionality (vps23, late endosomal trafficking) revealed a complex and interrelated protein collection. Semi-quantitative analysis of protein abundance revealed that mutations in both MVB- and Golgi-derived pathways affected the composition of yeast extracellular vesicles, but none abrogated vesicle production. Lipid analysis revealed that mutants with defects in Golgi-related components of the secretory pathway had slower vesicle release kinetics, as inferred from intracellular accumulation of sterols and reduced detection of these lipids in vesicle fractions in comparison with WT cells. Conclusions/Significance: Our results suggest that both conventional and unconventional pathways of secretion are required for biogenesis of extracellular vesicles, which demonstrate the complexity of this process in the biology of yeast cells.
机译:背景:酵母细胞中的细胞外囊泡参与细胞壁的分子运输。在酵母病原体中,这些囊泡与蛋白质,脂质,多糖和色素向细胞外空间的转运有关。酵母细胞外囊泡生物发生所需的细胞途径在很大程度上是未知的。方法/主要发现:我们利用透射电子显微镜结合光散射分析,脂质提取和蛋白质组学,对野生型(WT)和模型酵母酿酒酵母突变株的细胞外囊泡生产进行了表征。平行分析了具有Sec4p缺陷表达的WT细胞和突变体,Sec4p是高尔基衍生的胞吐作用所必需的一种分泌性囊泡相关的Rab GTP酶或Snf7p,它参与了多囊泡体(MVB)的形成。在酵母培养物的细胞外级分中发现了直径在100-300 nm范围内的双层囊泡。对上述细胞的囊泡部分进行蛋白质组学分析,以及在常规分泌途径中存在缺陷的其他突变体(sec1-1,高尔基体细胞外囊泡与质膜融合; bos1-1,靶向高尔基体的囊泡)或MVB功能( vps23,晚期内体运输)揭示了一个复杂且相互关联的蛋白质集合。蛋白质丰度的半定量分析表明,MVB和高尔基体来源的途径中的突变均影响酵母细胞外囊泡的组成,但没有一个消除了囊泡的产生。脂质分析表明,与野生型细胞相比,从固醇的细胞内积累和减少了在脂质组分中对这些脂质的检测可以推断,在分泌途径的高尔基体相关成分中有缺陷的突变体具有较慢的囊泡释放动力学。结论/意义:我们的结果表明,常规和非常规的分泌途径都是细胞外囊泡生物发生所必需的,这表明了酵母细胞生物学中该过程的复杂性。

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