Laboratório de Estudos Integrados em Bioquímica Microbiana, Instituto de Microbiologia Professor Paulo de Góes, Rio de Janeiro, Rio de Janeiro, Brazil.
PLoS One. 2010 Jun 14;5(6):e11113. doi: 10.1371/journal.pone.0011113.
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.
酵母细胞中的细胞外囊泡参与了穿过细胞壁的分子运输。在酵母病原体中,这些囊泡被认为参与了蛋白质、脂质、多糖和色素向细胞外空间的运输。酵母细胞外囊泡生物发生所需的细胞途径在很大程度上尚不清楚。
方法/主要发现:我们使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,对模型酵母酿酒酵母的野生型(WT)和突变株中外泌体的产生进行了表征。同时分析了 WT 细胞和 Sec4p 表达缺陷的突变体,Sec4p 是一种分泌小泡相关 Rab GTPase,对高尔基体衍生的胞吐作用至关重要,或 Snf7p,它参与多泡体(MVB)的形成。在酵母培养物的细胞外部分中发现了直径在 100-300nm 范围内的双层囊泡。对来自上述细胞以及具有传统分泌途径缺陷的额外突变体(sec1-1,高尔基体衍生的胞吐小泡与质膜融合;bos1-1,囊泡靶向高尔基复合体)或 MVB 功能(vps23,晚期内体运输)的囊泡部分进行的蛋白质组学分析显示了一组复杂且相互关联的蛋白质。蛋白质丰度的半定量分析表明,MVB 和高尔基体衍生途径的突变都影响了酵母细胞外囊泡的组成,但没有一种突变会阻断囊泡的产生。脂质分析表明,在高尔基体相关分泌途径的突变体中,由于固醇的细胞内积累,以及与 WT 细胞相比,这些脂质在囊泡部分中的检测减少,导致囊泡释放动力学变慢。
结论/意义:我们的结果表明,传统和非常规分泌途径都需要用于细胞外囊泡的生物发生,这表明在酵母细胞的生物学中,这个过程非常复杂。