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High resolution imaging and analysis of extracellular vesicles using mass spectral imaging and machine learning.
Bamford, Sarah Elizabeth; Vassileff, Natasha; Spiers, Jereme G; Gardner, Wil; Winkler, David A; Muir, Benjamin W; Hill, Andrew F; Pigram, Paul J.
Afiliação
  • Bamford SE; Centre for Materials and Surface Science and Department of Mathematical and Physical Sciences La Trobe University Bundoora Victoria Australia.
  • Vassileff N; The Department of Biochemistry and Chemistry La Trobe Institute for Molecular Science La Trobe University Bundoora Victoria Australia.
  • Spiers JG; The Department of Biochemistry and Chemistry La Trobe Institute for Molecular Science La Trobe University Bundoora Victoria Australia.
  • Gardner W; 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.
  • Winkler DA; School of Medicine and Psychology, College of Health and Medicine The Australian National University Acton ACT Australia.
  • Muir BW; Centre for Materials and Surface Science and Department of Mathematical and Physical Sciences La Trobe University Bundoora Victoria Australia.
  • Hill AF; The Department of Biochemistry and Chemistry La Trobe Institute for Molecular Science La Trobe University Bundoora Victoria Australia.
  • Pigram PJ; Monash Institute of Pharmaceutical Sciences Monash University Parkville Victoria Australia.
J Extracell Biol ; 2(9): e110, 2023 Sep.
Article em En | MEDLINE | ID: mdl-38938371
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Extracell Biol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Extracell Biol Ano de publicação: 2023 Tipo de documento: Article