Evidence map›Paper›PMID 25096726›Full record

ArticleScientific reports2014

High-throughput monitoring of major cell functions by means of lensfree video microscopy.

S Vinjimore Kesavan, F Momey, O Cioni, B David-Watine, N Dubrulle, S Shorte, E Sulpice, D Freida, B Chalmond, J M Dinten and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.6field-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

24 citing papers in PubMed, 73 citations in OpenAlex.

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  9. TheRoyal Society open science · 2022
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  20. The Point-of-Care Laboratory in Clinical Microbiology.Clinical microbiology reviews · 2016
    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

12 authors at 5 institutions in 1 country.

S Vinjimore Kesavan1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, LETI, MINATEC Campus, F-38054 Grenoble, France.
F Momey1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, LETI, MINATEC Campus, F-38054 Grenoble, France.
O Cioni1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, LETI, MINATEC Campus, F-38054 Grenoble, France.
B David-WatinePlateforme d'imagerie dynamique, Imagopole, Institut Pasteur, Paris, France.
N DubrullePlateforme d'imagerie dynamique, Imagopole, Institut Pasteur, Paris, France.
S ShortePlateforme d'imagerie dynamique, Imagopole, Institut Pasteur, Paris, France.
E Sulpice1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, iRTSV-Biologie à Grande Echelle, F-38054 Grenoble, France [3] INSERM, U1038, F-38054 Grenoble, France.
D Freida1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, iRTSV-Biologie à Grande Echelle, F-38054 Grenoble, France [3] INSERM, U1038, F-38054 Grenoble, France.
B Chalmond1] University of Cergy-Pontoise, France [2] CMLA, ENS Cachan, France.
J M Dinten1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, LETI, MINATEC Campus, F-38054 Grenoble, France.
X Gidrol1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, iRTSV-Biologie à Grande Echelle, F-38054 Grenoble, France [3] INSERM, U1038, F-38054 Grenoble, France [4].
C Allier1] Univ. Grenoble Alpes, F-38000 Grenoble, France [2] CEA, LETI, MINATEC Campus, F-38054 Grenoble, France [3].
Université Grenoble Alpes · FRInstitut Pasteur · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRCY Cergy Paris Université · FRLaboratoire Biologie à Grande Échelle · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantification of basic cell functions is a preliminary step to understand complex cellular mechanisms, for e.g., to test compatibility of biomaterials, to assess the effectiveness of drugs and siRNAs, and to control cell behavior. However, commonly used quantification methods are label-dependent, and end-point assays. As an alternative, using our lensfree video microscopy platform to perform high-throughput real-time monitoring of cell culture, we introduce specifically devised metrics that are capable of non-invasive quantification of cell functions such as cell-substrate adhesion, cell spreading, cell division, cell division orientation and cell death. Unlike existing methods, our platform and associated metrics embrace entire population of thousands of cells whilst monitoring the fate of every single cell within the population. This results in a high content description of cell functions that typically contains 25,000 - 900,000 measurements per experiment depending on cell density and period of observation. As proof of concept, we monitored cell-substrate adhesion and spreading kinetics of human Mesenchymal Stem Cells (hMSCs) and primary human fibroblasts, we determined the cell division orientation of hMSCs, and we observed the effect of transfection of siCellDeath (siRNA known to induce cell death) on hMSCs and human Osteo Sarcoma (U2OS) Cells.

Indexed as

Cell AdhesionCell CountCell DeathCell DivisionCell Line, TumorFibroblastsHumansMesenchymal Stem CellsMicroscopy, VideoOsteoblastsPrimary Cell CultureRNA, Small InterferingVideo RecordingRNA, Small Interfering

Identifiers

PMID25096726
PMCPMC5380008
OpenAlexW2055356103

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.