Evidence map›Paper›PMID 38510433›Full record

ArticleBiological imaging2022

3D cell morphology detection by association for embryo heart morphogenesis.

Rituparna Sarkar, Daniel Darby, Sigolène Meilhac, Jean-Christophe Olivo-Marin

Abstract read
In one paragraph

Article in Biological imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

4 authors.

Rituparna SarkarBioImage Analysis Unit, Institut Pasteur, Paris, France.ORCID https://orcid.org/0000-0001-7828-1816
Daniel DarbyUnit of Heart Morphogenesis, Imagine-Institut Pasteur, Paris, France.
Sigolène MeilhacUnit of Heart Morphogenesis, Imagine-Institut Pasteur, Paris, France.
Jean-Christophe Olivo-MarinBioImage Analysis Unit, Institut Pasteur, Paris, France.ORCID https://orcid.org/0000-0001-6796-0696

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advances in tissue engineering for cardiac regenerative medicine require cellular-level understanding of the mechanism of cardiac muscle growth during embryonic developmental stage. Computational methods to automatize cell segmentation in 3D and deliver accurate, quantitative morphology of cardiomyocytes, are imperative to provide insight into cell behavior underlying cardiac tissue growth. Detecting individual cells from volumetric images of dense tissue, poised with low signal-to-noise ratio and severe intensity in homogeneity, is a challenging task. In this article, we develop a robust segmentation tool capable of extracting cellular morphological parameters from 3D multifluorescence images of murine heart, captured via light-sheet microscopy. The proposed pipeline incorporates a neural network for 2D detection of nuclei and cell membranes. A graph-based global association employs the 2D nuclei detections to reconstruct 3D nuclei. A novel optimization embedding the network flow algorithm in an alternating direction method of multipliers is proposed to solve the global object association problem. The associated 3D nuclei serve as the initialization of an active mesh model to obtain the 3D segmentation of individual myocardial cells. The efficiency of our method over the state-of-the-art methods is observed via various qualitative and quantitative evaluation.

Indexed as

3D cell segmentationdata associationdevelopmental biologylight-sheet microscopymin-cost network flowmouse embryo

Identifiers

PMID38510433
PMCPMC10951799

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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.