High resolution imaging and analysis of extracellular vesicles using mass spectral imaging and machine learning

Sarah Elizabeth Bamford, Natasha Vassileff, Jereme G. Spiers, Wil Gardner, David A. Winkler, Benjamin W. Muir, Andrew F. Hill, Paul J. Pigram
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Abstract

Extracellular vesicles (EVs) are potentially useful biomarkers for disease detection and monitoring. Development of a label-free technique for imaging and distinguishing small volumes of EVs from different cell types and cell states would be of great value. Here, we have designed a method to explore the chemical changes in EVs associated with neuroinflammation using Time-of-Flight Secondary Ion Mass spectrometry (ToF-SIMS) and machine learning (ML). Mass spectral imaging was able to identify and differentiate EVs released by microglia following lipopolysaccharide (LPS) stimulation compared to a control group. This process requires a much smaller sample size (1 µL) than other molecular analysis methods (up to 50 µL). Conspicuously, we saw a reduction in free cysteine thiols (a marker of cellular oxidative stress associated with neuroinflammation) in EVs from microglial cells treated with LPS, consistent with the reduced cellular free thiol levels measured experimentally. This validates the synergistic combination of ToF-SIMS and ML as a sensitive and valuable technique for collecting and analysing molecular data from EVs at high resolution.

Abstract Image

利用质谱成像和机器学习对细胞外小泡进行高分辨率成像和分析
细胞外小泡(EVs)是用于疾病检测和监测的潜在有用的生物标志物。开发一种用于成像和区分不同细胞类型和细胞状态的小体积EV的无标记技术将具有巨大价值。在这里,我们设计了一种方法,使用飞行时间二次离子质谱(ToF-SIMS)和机器学习(ML)来探索与神经炎症相关的EV的化学变化。与对照组相比,质谱成像能够识别和区分脂多糖(LPS)刺激后小胶质细胞释放的EVs。该过程需要比其他分子分析方法(高达50µL)小得多的样本量(1µL)。值得注意的是,我们发现用LPS处理的小胶质细胞的EVs中游离半胱氨酸硫醇(与神经炎症相关的细胞氧化应激的标志物)减少,这与实验测量的细胞游离硫醇水平减少一致。这验证了ToF-SIMS和ML的协同组合是一种敏感而有价值的技术,用于以高分辨率收集和分析电动汽车的分子数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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