Evidence map›Paper›PMID 33863936›Full record

ArticleScientific reports2021

Self-organization and culture of Mesenchymal Stem Cell spheroids in acoustic levitation.

Nathan Jeger-Madiot, Lousineh Arakelian, Niclas Setterblad, Patrick Bruneval, Mauricio Hoyos, Jérôme Larghero, Jean-Luc Aider

Erratum issuedAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
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  4. Review
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  6. Article
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  8. Article
  9. 3D Culture of MSCs for Clinical Application.Bioengineering (Basel, Switzerland) · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. AnMaterials today. Bio · 2023
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Active matter in space.NPJ microgravity · 2022
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Nathan Jeger-MadiotLaboratoire de Physique et Mécanique des Milieux Hétérogènes (PMMH), UMR 7636 CNRS, ESPCI Paris, PSL, Paris Sciences et Lettres University, Sorbonne Université, Université de Paris 1, Paris, 75005, France. nathan.jeger-madiot@espci.fr.
Lousineh ArakelianUnité de Thérapie Cellulaire, APHP, Hôpital Saint-Louis, 1 avenue Claude Vellefaux, 75010, Paris, France. lousineh.arakelian@aphp.fr.
Niclas SetterbladTechnological Core facility of the Institut de Recherche Saint-Louis, Université Paris-Diderot and Inserm, Hôpital Saint-Louis, Paris, France.
Patrick BrunevalINSERM U970-PARCC, Paris, France.
Mauricio HoyosLaboratoire de Physique et Mécanique des Milieux Hétérogènes (PMMH), UMR 7636 CNRS, ESPCI Paris, PSL, Paris Sciences et Lettres University, Sorbonne Université, Université de Paris 1, Paris, 75005, France.
Jérôme LargheroUnité de Thérapie Cellulaire, APHP, Hôpital Saint-Louis, 1 avenue Claude Vellefaux, 75010, Paris, France.
Jean-Luc AiderLaboratoire de Physique et Mécanique des Milieux Hétérogènes (PMMH), UMR 7636 CNRS, ESPCI Paris, PSL, Paris Sciences et Lettres University, Sorbonne Université, Université de Paris 1, Paris, 75005, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, 3D cell culture models such as spheroid or organoid technologies have known important developments. Many studies have shown that 3D cultures exhibit better biomimetic properties compared to 2D cultures. These properties are important for in-vitro modeling systems, as well as for in-vivo cell therapies and tissue engineering approaches. A reliable use of 3D cellular models still requires standardized protocols with well-controlled and reproducible parameters. To address this challenge, a robust and scaffold-free approach is proposed, which relies on multi-trap acoustic levitation. This technology is successfully applied to Mesenchymal Stem Cells (MSCs) maintained in acoustic levitation over a 24-h period. During the culture, MSCs spontaneously self-organized from cell sheets to cell spheroids with a characteristic time of about 10 h. Each acoustofluidic chip could contain up to 30 spheroids in acoustic levitation and four chips could be ran in parallel, leading to the production of 120 spheroids per experiment. Various biological characterizations showed that the cells inside the spheroids were viable, maintained the expression of their cell surface markers and had a higher differentiation capacity compared to standard 2D culture conditions. These results open the path to long-time cell culture in acoustic levitation of cell sheets or spheroids for any type of cells.

Indexed as

AcousticsCell DifferentiationSpheroids, CellularCell Culture TechniquesCell ProliferationCells, CulturedCell SurvivalFluoresceinsHumansMesenchymal Stem CellsPropidiumTime FactorsTissue EngineeringFluoresceinsfluorexonPropidium

Identifiers

PMID33863936
PMCPMC8052426

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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.