Human Umbilical Cord Blood Endothelial Progenitor Cell-Derived Extracellular Vesicles Control Important Endothelial Cell Functions.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
07 Jun 2023
Historique:
received: 05 05 2023
revised: 02 06 2023
accepted: 05 06 2023
medline: 29 6 2023
pubmed: 28 6 2023
entrez: 28 6 2023
Statut: epublish

Résumé

Circulating endothelial progenitor cells (EPCs) play a pivotal role in the repair of diseases in which angiogenesis is required. Although they are a potentially valuable cell therapy tool, their clinical use remains limited due to suboptimal storage conditions and, especially, long-term immune rejection. EPC-derived extracellular vesicles (EPC-EVs) may be an alternative to EPCs given their key role in cell-cell communication and expression of the same parental markers. Here, we investigated the regenerative effects of umbilical cord blood (CB) EPC-EVs on CB-EPCs in vitro. After amplification, EPCs were cultured in a medium containing an EVs-depleted serum (EV-free medium). Then, EVs were isolated from the conditioned medium with tangential flow filtration (TFF). The regenerative effects of EVs on cells were investigated by analyzing cell migration, wound healing, and tube formation. We also analyzed their effects on endothelial cell inflammation and Nitric Oxide (NO) production. We showed that adding different doses of EPC-EVs on EPCs does not alter the basal expression of the endothelial cell markers nor change their proliferative potential and NO production level. Furthermore, we demonstrated that EPC-EVs, when used at a higher dose than the physiological dose, create a mild inflammatory condition that activates EPCs and boosts their regenerative features. Our results reveal for the first time that EPC-EVs, when used at a high dose, enhance EPC regenerative functions without altering their endothelial identity.

Identifiants

pubmed: 37373015
pii: ijms24129866
doi: 10.3390/ijms24129866
pmc: PMC10297996
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Sawssen Ben Fraj (S)

National Institute of Applied Sciences and Technology (INSAT), Carthage University, Tunis 1080, Tunisia.
INSERM UMR-S-MD 1197, Hôpital Paul Brousse, 94800 Villejuif, France.
LR18ES40, Inflammation, Environment and Signalization Pathologies, Faculty of Medicine, University of Monastir, Monastir 5000, Tunisia.

Sina Naserian (S)

INSERM UMR-S-MD 1197, Hôpital Paul Brousse, 94800 Villejuif, France.
CellMedEx, 94100 Saint Maur Des Fossés, France.

Bileyle Lorenzini (B)

INSERM UMR-S-MD 1197, Hôpital Paul Brousse, 94800 Villejuif, France.

Sylvie Goulinet (S)

INSERM UMR-S-MD 1197, Hôpital Paul Brousse, 94800 Villejuif, France.

Philippe Mauduit (P)

INSERM UMR-S-MD 1197, Hôpital Paul Brousse, 94800 Villejuif, France.

Georges Uzan (G)

INSERM UMR-S-MD 1197, Hôpital Paul Brousse, 94800 Villejuif, France.

Houda Haouas (H)

National Institute of Applied Sciences and Technology (INSAT), Carthage University, Tunis 1080, Tunisia.
LR18ES40, Inflammation, Environment and Signalization Pathologies, Faculty of Medicine, University of Monastir, Monastir 5000, Tunisia.

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