Evidence map›Paper›PMID 39530646›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2025

High-Yield Bioproduction of Extracellular Vesicles from Stem Cell Spheroids via Millifluidic Vortex Transport.

Elliot Thouvenot, Laura Charnay, Noa Burshtein, Jean-Michel Guigner, Léonie Dec, Damarys Loew, Amanda K A Silva, Anke Lindner, Claire Wilhelm

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Multiphysics-Driven Assembly of Biomimetic Vesicles.Advanced materials (Deerfield Beach, Fla.) · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. 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

9 authors.

Elliot ThouvenotLaboratoire Physique des Cellules et Cancer, PCC, CNRS UMR168, Institut Curie, Sorbonne Université, PSL Research University, Paris, 75005, France.ORCID https://orcid.org/0000-0003-2931-3249
Laura CharnayLaboratoire Physique des Cellules et Cancer, PCC, CNRS UMR168, Institut Curie, Sorbonne Université, PSL Research University, Paris, 75005, France.ORCID https://orcid.org/0000-0002-2896-1773
Noa BurshteinLaboratoire de Physique et Mécanique des Milieux Hétérogènes, PMMH, CNRS UMR7636, ESPCI Paris, PSL Research University, Sorbonne Université, Université Paris Cité, Paris, 75005, France.ORCID https://orcid.org/0000-0003-2910-6493
Jean-Michel GuignerInstitut de Minéralogie, de Physique des Matériaux et de Cosmochimie (IMPMC), UMR CNRS 7590, MNHN, IRD UR 206, Campus Jussieu, Sorbonne Université, Case courrier 115, 4 Place Jussieu, 75252, Paris, Cedex 05, France.
Léonie DecInstitut Curie, CurieCoreTech Mass Spectrometry Proteomics, PSL Research University, Paris, France.ORCID https://orcid.org/0009-0008-2475-0275
Damarys LoewInstitut Curie, CurieCoreTech Mass Spectrometry Proteomics, PSL Research University, Paris, France.ORCID https://orcid.org/0000-0002-9111-8842
Amanda K A SilvaLaboratoire Matière et Systèmes Complexes, MSC, CNRS UMR7057, Université Paris Cité, Paris, 75006, France.ORCID https://orcid.org/0000-0002-7713-1813
Anke LindnerLaboratoire de Physique et Mécanique des Milieux Hétérogènes, PMMH, CNRS UMR7636, ESPCI Paris, PSL Research University, Sorbonne Université, Université Paris Cité, Paris, 75005, France.ORCID https://orcid.org/0000-0002-5007-9568
Claire WilhelmLaboratoire Physique des Cellules et Cancer, PCC, CNRS UMR168, Institut Curie, Sorbonne Université, PSL Research University, Paris, 75005, France.ORCID https://orcid.org/0000-0001-7024-9627

Funding

ERC Consolidator Grant PaDyFlow 682367HORIZON EUROPE European Research Council ERC-2019-CoG project NanoBioMade 865629Inserm 21CQ016-00ITMO Cancer of Aviesanla Région Île-de-France N°EX061034
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are emerging as novel therapeutics, particularly in cancer and degenerative diseases. Nevertheless, from both market and clinical viewpoints, high-yield production methods using minimal cell materials are still needed. Herein, a millifluidic cross-slot chip is proposed to induce high-yield release of biologically active EVs from less than three million cells. Depending on the flow rate, a single vortex forms in the outlet channels, exposing transported cellular material to high viscous stresses. Importantly, the chip accommodates producer cells within their physiological environment, such as human mesenchymal stem cells (hMSCs) spheroids, while facilitating their visualization and individual tracking within the vortex. This precise control of viscous stresses at the spheroid level allows for the release of up to 30000 EVs per cell at a Reynolds number of ≈400, without compromising cellular integrity. Additionally, it reveals a threshold initiating EV production, providing evidence for a stress-dependent mechanism governing vesicle secretion. EVs mass-produced at high Reynolds displayed pro-angiogenic and wound healing capabilities, as confirmed by proteomic and cytometric analysis of their cargo. These distinct molecular signatures of these EVs, compared to those derived from monolayers, underscore the critical roles of the production method and the 3D cellular environment in EV generation.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsSpheroids, CellularHumansbioproductioncross‐slot chipextracellular vesiclesstem cell spheroidsvortex dynamics

Identifiers

PMID39530646
PMCPMC12087746

What OpenQuestion holds

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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.