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首页> 外文期刊>Journal of Extracellular Vesicles >Proteomic characterisation of leech microglia extracellular vesicles (EVs): comparison between differential ultracentrifugation and Optiprep? density gradient isolation
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Proteomic characterisation of leech microglia extracellular vesicles (EVs): comparison between differential ultracentrifugation and Optiprep? density gradient isolation

机译:水ech小胶质细胞外囊泡(EVs)的蛋白质组学表征:差异超速离心和Optiprep?的比较密度梯度隔离

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ABSTRACT In Mammals, microglial cells are considered as the resident immune cells in central nervous system (CNS). Many studies demonstrated that, after injury, these cells are activated and recruited at the lesion site. Leech microglia present a similar pattern of microglial activation and migration upon experimental lesion of CNS. This activation is associated with the release of a large amount of extracellular vesicles (EVs). We collected EVs released by microglia primary culture and compared two different protocols of isolation: one with differential ultracentrifugation (UC) and one using an additional Optiprep ? Density Gradient (ODG) ultracentrifugation. Nanoparticles tracking analysis (NTA) and transmission electron microscopy (TEM) were used to assess vesicles size and morphology. The protein content of isolated EVs was assessed by mass spectrometry approaches. Results showed the presence of EV-specific proteins in both procedures. The extensive proteomic analysis of each single ODG fractions confirmed the efficiency of this protocol in limiting the presence of co-isolated proteins aggregates and other membranous particles during vesicles isolation. The present study permitted for the first time the characterisation of microglial EV protein content in an annelid model. Interestingly, an important amount of proteins found in leech vesicles was previously described in EV-specific databases. Finally, purified EVs were assessed for neurotrophic activity and promote neurites outgrowth on primary cultured neurons.
机译:摘要在哺乳动物中,小胶质细胞被认为是中枢神经系统(CNS)的固有免疫细胞。许多研究表明,受伤后这些细胞被激活并募集到病变部位。水experimental小胶质细胞在中枢神经系统的实验性病变时表现出类似的小胶质细胞活化和迁移模式。这种激活与大量细胞外囊泡(EVs)的释放有关。我们收集了由小胶质细胞原代培养释放的EV,并比较了两种不同的分离方案:一种采用差速超速离心(UC),另一种采用额外的Optiprep?密度梯度(ODG)超速离心。纳米粒子跟踪分析(NTA)和透射电子显微镜(TEM)用于评估囊泡的大小和形态。通过质谱法评估分离的电动汽车的蛋白质含量。结果表明两种方法均存在EV特异性蛋白。每个ODG组分的蛋白质组学广泛分析证实了该方案在限制囊泡分离过程中共分离蛋白聚集体和其他膜状颗粒的存在方面的有效性。本研究首次允许在神经胶质瘤模型中表征小胶质EV蛋白含量。有趣的是,先前在EV专用数据库中描述了在水ech小泡中发现的大量蛋白质。最后,评估纯电动车的神经营养活性并促进神经元在原代培养神经元上的生长。

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