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

Author:

Bamford Sarah Elizabeth1,Vassileff Natasha2,Spiers Jereme G.234ORCID,Gardner Wil1,Winkler David A.256,Muir Benjamin W.7,Hill Andrew F.28ORCID,Pigram Paul J.1ORCID

Affiliation:

1. Centre for Materials and Surface Science and Department of Mathematical and Physical Sciences La Trobe University Bundoora Victoria Australia

2. The Department of Biochemistry and Chemistry La Trobe Institute for Molecular Science La Trobe University Bundoora Victoria Australia

3. Clear Vision Research, Eccles Institute of Neuroscience, John Curtin School of Medical Research, College of Health and Medicine The Australian National University Acton ACT Australia

4. School of Medicine and Psychology, College of Health and Medicine The Australian National University Acton ACT Australia

5. Monash Institute of Pharmaceutical Sciences Monash University Parkville Victoria Australia

6. School of Pharmacy University of Nottingham Nottingham UK

7. CSIRO Manufacturing Clayton Victoria Australia

8. Institute for Health and Sport Victoria University Victoria Australia

Abstract

AbstractExtracellular 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.

Funder

Australian National Fabrication Facility

National Health and Medical Research Council

Publisher

Wiley

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