Evidence map›Paper›PMID 39400522›Full record

ArticleJournal of extracellular vesicles2024

Low fluid shear stress stimulates the uptake of noxious endothelial extracellular vesicles via MCAM and PECAM-1 cell adhesion molecules.

Pierre-Michaël Coly, Shruti Chatterjee, Fariza Mezine, Christelle El Jekmek, Cécile Devue, Thomas Nipoti, Stephane Mazlan, Maribel Lara Corona, Florent Dingli, Damarys Loew and 3 more

Abstract read
In one paragraph

Article in Journal of extracellular vesicles, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Vascular Mechanobiology: From Membrane to Nucleus.Advances in experimental medicine and biology · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. 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

13 authors.

Pierre-Michaël ColyUniversité Paris-Cité, PARCC, INSERM, Paris, France.ORCID 0000-0002-4425-8375
Shruti ChatterjeeUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Fariza MezineUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Christelle El JekmekUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Cécile DevueUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Thomas NipotiUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Stephane MazlanUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Maribel Lara CoronaInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM, Paris, France.
Florent DingliInstitut Curie, PSL Research University, Centre de Recherche, CurieCoreTech Spectrométrie de Masse Protéomique, Paris, France.
Damarys LoewInstitut Curie, PSL Research University, Centre de Recherche, CurieCoreTech Spectrométrie de Masse Protéomique, Paris, France.ORCID 0000-0002-9111-8842
Guillaume van NielInstitute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM, Paris, France.
Xavier LoyerUniversité Paris-Cité, PARCC, INSERM, Paris, France.
Chantal M BoulangerUniversité Paris-Cité, PARCC, INSERM, Paris, France.

Funding

Agence Nationale de la Recherche ANR-16-CE14-0015-01Agence Nationale de la Recherche ANR-16-CE92-0032-02Agence Nationale de la Recherche ANR-20-CE18-0026-01Fondation pour la Recherche Médicale EQU202003010767H2020 Marie Skłodowska-Curie Actions 665850Institut National Du Cancer INCA-PLBIO19-059
6 · The paper itself

Abstract

Atherosclerotic lesions mainly form in arterial areas exposed to low shear stress (LSS), where endothelial cells express a senescent and inflammatory phenotype. Conversely, areas exposed to high shear stress (HSS) are protected from plaque development. Endothelial extracellular vesicles (EVs) have been shown to regulate inflammation and senescence, and therefore play a crucial role in vascular homeostasis. Whilst previous studies have shown links between hemodynamic forces and EV release, the effects of shear stress on the release and uptake of endothelial EVs remains elusive. We aim to decipher the interplay between these processes in endothelial cells exposed to atheroprone or atheroprotective shear stress. Confluent HUVECs were exposed to LSS or HSS for 24 h. Large and small EVs were isolated from conditioned medium by centrifugation and size exclusion chromatography. They were characterised by TEM, Western blot, tunable resistive pulse sensing, flow cytometry and proteomics. Uptake experiments were performed using fluorescently-labelled EVs and differences between groups were assessed by flow cytometry and confocal microscopy. We found that levels of large and small EVs in conditioned media were fifty and five times higher in HSS than in LSS conditions, respectively. In vivo and in vitro uptake experiments revealed greater EV incorporation by cells exposed to LSS conditions. Additionally, endothelial LSS-EVs have a greater affinity for HUVECs than HSS-EVs or EVs derived from platelets, erythrocytes and leukocytes. Proteomic analysis revealed that LSS-EVs were enriched in adhesion proteins (PECAM1, MCAM), participating in EV uptake by endothelial cells. LSS-EVs also carried mitochondrial material, which may be implicated in elevating ROS levels in recipient cells. These findings suggest that shear stress influences EV biogenesis and uptake. Given the major role of EVs and shear stress in vascular health, deciphering the relation between these processes may yield innovative strategies for the early detection and treatment of endothelial dysfunction.

Indexed as

Extracellular VesiclesHuman Umbilical Vein Endothelial CellsPlatelet Endothelial Cell Adhesion Molecule-1Stress, MechanicalEndothelial CellsHumansPECAM1 protein, humanPlatelet Endothelial Cell Adhesion Molecule-1endothelial cellsextracellular vesiclesMCAMmitochondriaPECAM1shear stressuptake

Identifiers

PMID39400522
PMCPMC11472237

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.