Evidence map›Paper›PMID 32373878›Full record

ArticleJournal of materials chemistry. B2020

Molecular imaging of extracellular vesicles in vitro via Raman metabolic labelling.

Conor C Horgan, Anika Nagelkerke, Thomas E Whittaker, Valeria Nele, Lucia Massi, Ulrike Kauscher, Jelle Penders, Mads S Bergholt, Steve R Hood, Molly M Stevens

Open access · hybridAbstract read
In one paragraph

Article in Journal of materials chemistry. B, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Application of Single Extracellular Vesicle Analysis Techniques.International journal of nanomedicine · 2023
    Review
  10. Review
  11. Tracking tools of extracellular vesicles for biomedical research.Frontiers in bioengineering and biotechnology · 2022
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Conor C HorganDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0003-0495-1615
Anika NagelkerkeDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.
Thomas E WhittakerDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0002-3181-4571
Valeria NeleDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0002-7263-7209
Lucia MassiDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.
Ulrike KauscherDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0002-2681-5692
Jelle PendersDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0002-5232-917X
Mads S BergholtDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0003-3986-8942
Steve R HoodGSK Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, UK.
Molly M StevensDepartment of Materials, Imperial College London, London SW7 2AZ, UK. m.stevens@imperial.ac.uk and Department of Bioengineering, Imperial College London, London SW7 2AZ, UK and Institute of Biomedical Engineering, Imperial College London, London SW7 2AZ, UK.ORCID 0000-0002-7335-266X
NIHR Imperial Biomedical Research Centre · GBUniversity of Hertfordshire · GB

Funding

Wellcome Trust 098411Wellcome Trust 098411/Z/12/Z
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are biologically-derived nanovectors important for intercellular communication and trafficking. As such, EVs show great promise as disease biomarkers and therapeutic drug delivery vehicles. However, despite the rapidly growing interest in EVs, understanding of the biological mechanisms that govern their biogenesis, secretion, and uptake remains poor. Advances in this field have been hampered by both the complex biological origins of EVs, which make them difficult to isolate and identify, and a lack of suitable imaging techniques to properly study their diverse biological roles. Here, we present a new strategy for simultaneous quantitative in vitro imaging and molecular characterisation of EVs in 2D and 3D based on Raman spectroscopy and metabolic labelling. Deuterium, in the form of deuterium oxide (D2O), deuterated choline chloride (d-Chol), or deuterated d-glucose (d-Gluc), is metabolically incorporated into EVs through the growth of parent cells on medium containing one of these compounds. Isolated EVs are thus labelled with deuterium, which acts as a bio-orthogonal Raman-active tag for direct Raman identification of EVs when introduced to unlabelled cell cultures. Metabolic deuterium incorporation demonstrates no apparent adverse effects on EV secretion, marker expression, morphology, or global composition, indicating its capacity for minimally obstructive EV labelling. As such, our metabolic labelling strategy could provide integral insights into EV biocomposition and trafficking. This approach has the potential to enable a deeper understanding of many of the biological mechanisms underpinning EVs, with profound implications for the design of EVs as therapeutic delivery vectors and applications as disease biomarkers.

Indexed as

Molecular ImagingSpectrum Analysis, RamanCholineDeuterium OxideExtracellular VesiclesGlucoseHumansParticle SizeSurface PropertiesTumor Cells, CulturedCholineDeuterium OxideGlucose

Identifiers

PMID32373878
PMCPMC7610785
OpenAlexW3021523471

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.