Evidence map›Paper›PMID 26459014›Full record

ArticleScientific reports2015

Time-lapse contact microscopy of cell cultures based on non-coherent illumination.

Marion Gabriel, Dorothée Balle, Stéphanie Bigault, Cyrille Pornin, Stéphane Gétin, François Perraut, Marc R Block, François Chatelain, Nathalie Picollet-D'hahan, Xavier Gidrol and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Dienone Compounds: Targets and Pharmacological Responses.Journal of medicinal chemistry · 2020
    Article
  2. 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

11 authors at 4 institutions in 1 country.

Marion GabrielCEA, iRTSV-BGE, F-38000 Grenoble, France.
Dorothée BalleCEA, iRTSV-BGE, F-38000 Grenoble, France.
Stéphanie BigaultCEA, iRTSV-BGE, F-38000 Grenoble, France.
Cyrille PorninCEA, Léti-DOPT, F-38000 Grenoble, France.
Stéphane GétinCEA, Léti-DOPT, F-38000 Grenoble, France.
François PerrautCEA, Léti-DTBS, F-38000 Grenoble, France.
Marc R BlockIAB, CRI INSERM/UJF U823, 38706 La Tronche, France.
François ChatelainCEA, IBS, F-38000 Grenoble, France.
Nathalie Picollet-D'hahanCEA, iRTSV-BGE, F-38000 Grenoble, France.
Xavier GidrolCEA, iRTSV-BGE, F-38000 Grenoble, France.
Vincent HaguetCEA, iRTSV-BGE, F-38000 Grenoble, France.
CEA Grenoble · FRInserm · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRInstitut de Biologie Structurale · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Video microscopy offers outstanding capabilities to investigate the dynamics of biological and pathological mechanisms in optimal culture conditions. Contact imaging is one of the simplest imaging architectures to digitally record images of cells due to the absence of any objective between the sample and the image sensor. However, in the framework of in-line holography, other optical components, e.g., an optical filter or a pinhole, are placed underneath the light source in order to illuminate the cells with a coherent or quasi-coherent incident light. In this study, we demonstrate that contact imaging with an incident light of both limited temporal and spatial coherences can be achieved with sufficiently high quality for most applications in cell biology, including monitoring of cell sedimentation, rolling, adhesion, spreading, proliferation, motility, death and detachment. Patterns of cells were recorded at various distances between 0 and 1000 μm from the pixel array of the image sensors. Cells in suspension, just deposited or at mitosis focalise light into photonic nanojets which can be visualised by contact imaging. Light refraction by cells significantly varies during the adhesion process, the cell cycle and among the cell population in connection with every modification in the tridimensional morphology of a cell.

Indexed as

Cell AdhesionCell Culture TechniquesCell MovementCell ProliferationCells, CulturedHumansMicroscopy, VideoTime-Lapse Imaging

Identifiers

PMID26459014
PMCPMC4602279
OpenAlexW2416752428

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.