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首页> 外文期刊>Journal of Extracellular Vesicles >Proteomic analysis reveals procoagulant properties of cigarette smoke-induced extracellular vesicles
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Proteomic analysis reveals procoagulant properties of cigarette smoke-induced extracellular vesicles

机译:蛋白质组学分析显示香烟烟雾诱导的细胞外囊泡的促凝特性

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ABSTRACT Airway epithelial cells secrete extracellular vesicles (EVs) under basal conditions and when exposed to cigarette smoke extract (CSE). Getting insights into the composition of these EVs will help unravel their functions in homeostasis and smoking-induced pathology. Here, we characterized the proteomic composition of basal and CSE-induced airway epithelial EVs. BEAS-2B cells were left unexposed or exposed to 1% CSE for 24 h, followed by EV isolation using ultrafiltration and size exclusion chromatography. Isolated EVs were labelled with tandem mass tags and their proteomic composition was determined using nano-LC-MS/MS. Tissue factor (TF) activity was determined by a factor Xa generation assay, phosphatidylserine (PS) content by prothrombinase assay and thrombin generation using calibrated automated thrombogram (CAT). Nano-LC-MS/MS identified 585 EV-associated proteins with high confidence. Of these, 201 were differentially expressed in the CSE-EVs according to the moderated t -test, followed by false discovery rate (FDR) adjustment with the FDR threshold set to 0.1. Functional enrichment analysis revealed that 24 proteins of the pathway haemostasis were significantly up-regulated in CSE-EVs, including TF. Increased TF expression on CSE-EVs was confirmed by bead-based flow cytometry and was associated with increased TF activity. CSE-EVs caused faster and more thrombin generation in normal human plasma than control-EVs, which was partly TF-, but also PS-dependent. In conclusion, proteomic analysis allowed us to predict procoagulant properties of CSE-EVs which were confirmed in vitro . Cigarette smoke-induced EVs may contribute to the increased cardiovascular and respiratory risk observed in smokers.
机译:摘要气道上皮细胞在基础条件下以及暴露于香烟烟雾提取物(CSE)时会分泌细胞外囊泡(EVs)。深入了解这些电动汽车的组成将有助于阐明其在体内稳态和吸烟引起的病理中的功能。在这里,我们表征了基础和CSE诱导的气道上皮电动汽车的蛋白质组学组成。将BEAS-2B细胞不暴露或暴露于1%CSE中24小时,然后使用超滤和尺寸排阻色谱法进行EV分离。分离的电动汽车用串联质量标签标记,并使用纳米LC-MS / MS确定其蛋白质组学组成。通过凝血因子Xa生成测定法测定组织因子(TF)活性,通过凝血酶原酶测定法测定磷脂酰丝氨酸(PS)的含量,并使用校准的自动血栓图(CAT)测定凝血酶的产生。 Nano-LC-MS / MS以高可信度鉴定出585种与EV相关的蛋白质。其中,根据缓和的t检验在CSE-EV中差异表达201,然后在FDR阈值设置为0.1的情况下进行错误发现率(FDR)调整。功能富集分析显示,CSE-EV中包括TF在内的24种通路止血蛋白均显着上调。基于微珠的流式细胞术证实了CSE-EV上TF表达的增加,并且与TF活性增加有关。 CSE-EV在正常人血浆中的凝血酶生成速度比对照EV更快,更多,而对照EV则部分依赖TF,但也依赖PS。总之,蛋白质组学分析使我们能够预测在体外证实的CSE-EVs的促凝特性。香烟烟雾诱发的电动汽车可能会导致吸烟者心血管和呼吸系统风险增加。

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