Human Umbilical Cord Blood Endothelial Progenitor Cell-Derived Extracellular Vesicles Control Important Endothelial Cell Functions.
Sawssen Ben FrajSina NaserianBileyle LorenziniSylvie GoulinetPhilippe MauduitGeorges UzanHouda HaouasPublished in: International journal of molecular sciences (2023)
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.
Keyphrases
- cell therapy
- endothelial cells
- mesenchymal stem cells
- umbilical cord
- stem cells
- cord blood
- high dose
- high glucose
- nitric oxide
- cell migration
- poor prognosis
- single cell
- oxidative stress
- wound healing
- induced apoptosis
- low dose
- tissue engineering
- gene expression
- mass spectrometry
- cell cycle arrest
- risk assessment
- long non coding rna
- pi k akt
- hydrogen peroxide
- nucleic acid
- nitric oxide synthase
- endoplasmic reticulum stress
- high resolution
- dna methylation