Evidence map›Paper›PMID 32059013›Full record

ArticlePLoS computational biology2020

From whole-organ imaging to in-silico blood flow modeling: A new multi-scale network analysis for revisiting tissue functional anatomy.

Pol Kennel, Jules Dichamp, Corinne Barreau, Christophe Guissard, Lise Teyssedre, Jacques Rouquette, Julien Colombelli, Anne Lorsignol, Louis Casteilla, Franck Plouraboué

Abstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Molecular Mediated Angiogenesis and Vasculogenesis Networks.International journal of molecular sciences · 2025
    Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. 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

10 authors.

Pol KennelInstitute of Fluid Mechanics of Toulouse (IMFT), Toulouse University, CNRS, INPT, UPS, Toulouse, France.
Jules DichampInstitute of Fluid Mechanics of Toulouse (IMFT), Toulouse University, CNRS, INPT, UPS, Toulouse, France.
Corinne BarreauCNRS 5273; UMR STROMALab, BP 84225, F-31 432 Toulouse Cedex 4, France.
Christophe GuissardCNRS 5273; UMR STROMALab, BP 84225, F-31 432 Toulouse Cedex 4, France.
Lise TeyssedreITAV, Université de Toulouse, CNRS, UPS, France.
Jacques RouquetteITAV, Université de Toulouse, CNRS, UPS, France.
Julien ColombelliAdvanced Digital Microscopy Core Facility, Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology. C. Baldiri Reixac, 10. E-08028 Barcelona, Spain.
Anne LorsignolCNRS 5273; UMR STROMALab, BP 84225, F-31 432 Toulouse Cedex 4, France.
Louis CasteillaCNRS 5273; UMR STROMALab, BP 84225, F-31 432 Toulouse Cedex 4, France.
Franck PlourabouéInstitute of Fluid Mechanics of Toulouse (IMFT), Toulouse University, CNRS, INPT, UPS, Toulouse, France.ORCID 0000-0003-0349-4221

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a multi-disciplinary image-based blood flow perfusion modeling of a whole organ vascular network for analyzing both its structural and functional properties. We show how the use of Light-Sheet Fluorescence Microscopy (LSFM) permits whole-organ micro-vascular imaging, analysis and modelling. By using adapted image post-treatment workflow, we could segment, vectorize and reconstruct the entire micro-vascular network composed of 1.7 million vessels, from the tissue-scale, inside a ∼ 25 × 5 × 1 = 125mm3 volume of the mouse fat pad, hundreds of times larger than previous studies, down to the cellular scale at micron resolution, with the entire blood perfusion modeled. Adapted network analysis revealed the structural and functional organization of meso-scale tissue as strongly connected communities of vessels. These communities share a distinct heterogeneous core region and a more homogeneous peripheral region, consistently with known biological functions of fat tissue. Graph clustering analysis also revealed two distinct robust meso-scale typical sizes (from 10 to several hundred times the cellular size), revealing, for the first time, strongly connected functional vascular communities. These community networks support heterogeneous micro-environments. This work provides the proof of concept that in-silico all-tissue perfusion modeling can reveal new structural and functional exchanges between micro-regions in tissues, found from community clusters in the vascular graph.

Indexed as

Blood CirculationModels, BiologicalAnimalsComputer SimulationMaleMiceMice, Inbred C57BL

Identifiers

PMID32059013
PMCPMC7062279

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.