Evidence map›Paper›PMID 32314312›Full record

ArticleTissue engineering and regenerative medicine2020

Channeling Effect and Tissue Morphology in a Perfusion Bioreactor Imaged by X-Ray Microtomography.

Claire C Beauchesne, Morgan Chabanon, Benjamin Smaniotto, Benoît Ladoux, Benoît Goyeau, Bertrand David

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering and regenerative medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 62% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 3 institutions in 2 countries.

Claire C BeauchesneLab. EM2C, UPR CNRS 288, CentraleSupélec, Université Paris-Saclay, 3 rue Joliot-Curie, 91192, Gif-sur-Yvette Cedex, France.
Morgan ChabanonSingle Molecule Biophotonics Lab. ICFO, The Institute of Photonic Sciences, av. Carl Friedrich Gauss, 3, 08860, Castelldefels, Barcelona, Spain.
Benjamin SmaniottoENS Paris Saclay, LMT, CNRS, UMR 8535, 61 avenue du Président Wilson, 94230, Cachan, France.
Benoît LadouxInstitut Jacques Monod (IJM), UMR CNRS 7592, Université Paris Diderot, 15 rue Hélène Brion, 75013, Paris, France.
Benoît GoyeauLab. EM2C, UPR CNRS 288, CentraleSupélec, Université Paris-Saclay, 3 rue Joliot-Curie, 91192, Gif-sur-Yvette Cedex, France. benoit.goyeau@centralesupelec.fr.ORCID http://orcid.org/0000-0003-1642-1558
Bertrand DavidLab. MSSMat, UMR CNRS 8579, CentraleSupélec, Université Paris-Saclay, 3 rue Joliot-Curie, 91192, Gif-sur-Yvette Cedex, France.
Centre National de la Recherche Scientifique · FRÉcole Normale Supérieure Paris-Saclay · FRInstitute of Photonic Sciences · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPerfusion bioreactors for tissue engineering hold great promises. Indeed, the perfusion of culture medium enhances species transport and mechanically stimulates the cells, thereby increasing cell proliferation and tissue formation. Nonetheless, their development is still hampered by a lack of understanding of the relationship between mechanical cues and tissue growth.

methodsCombining tissue engineering, three-dimensional visualization and numerical simulations, we analyze the morphological evolution of neo-tissue in a model bioreactor with respect to the local flow pattern. NIH-3T3 cells were grown under perfusion for one, two and three weeks on a stack of 2 mm polyacetal beads. The model bioreactor was then imaged by X-ray micro-tomography and local tissue morphology was analyzed. To relate experimental observations and mechanical stimulii, a computational fluid dynamics model of flow around spheres in a canal was developed and solved using the finite element method.

resultsWe observe a preferential tissue formation at the bioreactor periphery, and relate it to a channeling effect leading to regions of higher flow intensity. Additionally, we find that circular crater-like tissue patterns form in narrow channel regions at early culture times. Using computational fluid dynamic simulations, we show that the location and morphology of these patterns match those of shear stress maxima. Finally, the morphology of the tissue is qualitatively described as the tissue grows and reorganizes itself.

conclusionAltogether, our study points out the key role of local flow conditions on the tissue morphology developed on a stack of beads in perfusion bioreactors and provides new insights for effective design of hydrodynamic bioreactors for tissue engineering using bead packings.

Indexed as

BioreactorsPerfusionAnimalsCell Culture TechniquesCell ProliferationHydrodynamicsImaging, Three-DimensionalMiceNIH 3T3 CellsStress, MechanicalTissue EngineeringX-Ray MicrotomographyChanneling effectPerfusion bioreactorTissue engineeringTissue morphologyX-ray microtomography

Identifiers

PMID32314312
PMCPMC7260345
OpenAlexW3016709701

What OpenQuestion holds

Textmetadata
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.