Evidence map›Paper›PMID 36051442›Full record

ArticleFrontiers in cell and developmental biology2022

Coherent anti-Stokes Raman scattering cell imaging and segmentation with unsupervised data analysis.

Damien Boildieu, Tiffany Guerenne-Del Ben, Ludovic Duponchel, Vincent Sol, Jean-Michel Petit, Éric Champion, Hideaki Kano, David Helbert, Amandine Magnaudeix, Philippe Leproux and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.2field-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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. 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

11 authors at 4 institutions in 2 countries.

Damien BoildieuUniversity of Limoges, CNRS, XLIM, UMR 7252, Limoges, France.
Tiffany Guerenne-Del BenUniversity of Limoges, PEIRENE, UR 22722, Limoges, France.
Ludovic DuponchelUniversity of Lille, CNRS, UMR 8516, LASIRE - Laboratoire de Spectroscopie Pour Les Interactions, La Réactivité et L'Environnement, Lille, France.
Vincent SolUniversity of Limoges, PEIRENE, UR 22722, Limoges, France.
Jean-Michel PetitUniversity of Limoges, PEIRENE, UR 22722, Limoges, France.
Éric ChampionUniversity of Limoges, CNRS, Institut de Recherche sur Les Céramiques, UMR 7315, Limoges, France.
Hideaki KanoDepartment of Chemistry, Faculty of Science, Kyushu University, Fukuoka, Japan.
David HelbertUniversity of Poitiers, CNRS, XLIM, UMR 7252, Poitiers, France.
Amandine MagnaudeixUniversity of Limoges, CNRS, Institut de Recherche sur Les Céramiques, UMR 7315, Limoges, France.
Philippe LeprouxUniversity of Limoges, CNRS, XLIM, UMR 7252, Limoges, France.
Philippe CarréUniversity of Poitiers, CNRS, XLIM, UMR 7252, Poitiers, France.
Centre National de la Recherche Scientifique · FRUniversité de Limoges · FRKyushu University · JPUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coherent Raman imaging has been extensively applied to live-cell imaging in the last 2 decades, allowing to probe the intracellular lipid, protein, nucleic acid, and water content with a high-acquisition rate and sensitivity. In this context, multiplex coherent anti-Stokes Raman scattering (MCARS) microspectroscopy using sub-nanosecond laser pulses is now recognized as a mature and straightforward technology for label-free bioimaging, offering the high spectral resolution of conventional Raman spectroscopy with reduced acquisition time. Here, we introduce the combination of the MCARS imaging technique with unsupervised data analysis based on multivariate curve resolution (MCR). The MCR process is implemented under the classical signal non-negativity constraint and, even more originally, under a new spatial constraint based on cell segmentation. We thus introduce a new methodology for hyperspectral cell imaging and segmentation, based on a simple, unsupervised workflow without any spectrum-to-spectrum phase retrieval computation. We first assess the robustness of our approach by considering cells of different types, namely, from the human HEK293 and murine C2C12 lines. To evaluate its applicability over a broader range, we then study HEK293 cells in different physiological states and experimental situations. Specifically, we compare an interphasic cell with a mitotic (prophase) one. We also present a comparison between a fixed cell and a living cell, in order to visualize the potential changes induced by the fixation protocol in cellular architecture. Next, with the aim of assessing more precisely the sensitivity of our approach, we study HEK293 living cells overexpressing tropomyosin-related kinase B (TrkB), a cancer-related membrane receptor, depending on the presence of its ligand, brain-derived neurotrophic factor (BDNF). Finally, the segmentation capability of the approach is evaluated in the case of a single cell and also by considering cell clusters of various sizes.

Indexed as

cell imagingcell segmentationcoherent anti-Stokes Raman scatteringcoherent Raman imaginglabel-free imagingmultivariate curve resolutionsupercontinuumunsupervised data analysis

Identifiers

PMID36051442
PMCPMC9424763
OpenAlexW4291938955

What OpenQuestion holds

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Registered trials

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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.