Evidence map›Paper›PMID 27886235›Full record

ArticleScientific reports2016

Time-lapse 3-D measurements of a glucose biosensor in multicellular spheroids by light sheet fluorescence microscopy in commercial 96-well plates.

Vincent Maioli, George Chennell, Hugh Sparks, Tobia Lana, Sunil Kumar, David Carling, Alessandro Sardini, Chris Dunsby

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Recent advances in oblique plane microscopy.Nanophotonics (Berlin, Germany) · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Lasers in Live Cell Microscopy.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Dual-view oblique plane microscopy (dOPM).Biomedical optics express · 2020
    Article
  17. Review
  18. Article
  19. Probing pluripotency gene regulatory networks with quantitative live cell imaging.Computational and structural biotechnology journal · 2020
    Review
  20. Article
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

8 authors at 2 institutions in 1 country.

Vincent MaioliPhotonics Group, Department of Physics, Imperial College London, United Kingdom.
George ChennellPhotonics Group, Department of Physics, Imperial College London, United Kingdom.
Hugh SparksPhotonics Group, Department of Physics, Imperial College London, United Kingdom.
Tobia LanaMRC Clinical Sciences Centre (CSC), Du Cane Road, London, United Kingdom.
Sunil KumarPhotonics Group, Department of Physics, Imperial College London, United Kingdom.
David CarlingMRC Clinical Sciences Centre (CSC), Du Cane Road, London, United Kingdom.
Alessandro SardiniMRC Clinical Sciences Centre (CSC), Du Cane Road, London, United Kingdom.
Chris DunsbyPhotonics Group, Department of Physics, Imperial College London, United Kingdom.
Imperial College London · GBMRC Clinical Trials Unit at UCL · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I023801/1Biotechnology and Biological Sciences Research Council BB/M006786/1Medical Research Council MC_U120027537MRF_ MRF-023-0002-S-CHENN
6 · The paper itself

Abstract

Light sheet fluorescence microscopy has previously been demonstrated on a commercially available inverted fluorescence microscope frame using the method of oblique plane microscopy (OPM). In this paper, OPM is adapted to allow time-lapse 3-D imaging of 3-D biological cultures in commercially available glass-bottomed 96-well plates using a stage-scanning OPM approach (ssOPM). Time-lapse 3-D imaging of multicellular spheroids expressing a glucose Förster resonance energy transfer (FRET) biosensor is demonstrated in 16 fields of view with image acquisition at 10 minute intervals. As a proof-of-principle, the ssOPM system is also used to acquire a dose response curve with the concentration of glucose in the culture medium being varied across 42 wells of a 96-well plate with the whole acquisition taking 9 min. The 3-D image data enable the FRET ratio to be measured as a function of distance from the surface of the spheroid. Overall, the results demonstrate the capability of the OPM system to measure spatio-temporal changes in FRET ratio in 3-D in multicellular spheroids over time in a multi-well plate format.

Indexed as

Biosensing TechniquesSpheroids, CellularFluorescence Resonance Energy TransferGlucoseHEK293 CellsHumansMicroscopy, FluorescenceGlucose

Identifiers

PMID27886235
PMCPMC5122899
OpenAlexW2551453933

What OpenQuestion holds

Textmetadata
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.