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Review
. 2020 Jan 9:7:353.
doi: 10.3389/fcell.2019.00353. eCollection 2019.

Exosomes in the Regulation of Vascular Endothelial Cell Regeneration

Affiliations
Review

Exosomes in the Regulation of Vascular Endothelial Cell Regeneration

Jugajyoti Baruah et al. Front Cell Dev Biol. .

Abstract

Exosomes have been described as nanoscale membranous extracellular vesicles that emerge from a variety of cells and tissues and are enriched with biologically active genomic and non-genomic biomolecules capable of transducing cell to cell communication. Exosome release, and exosome mediated signaling and cross-talks have been reported in several pathophysiological states. Therefore, exosomes have the potential to become suitable for the diagnosis, prognosis and treatment of specific diseases, including endothelial cell (EC) dysfunction and regeneration. The role of EC-derived exosomes in the mechanisms of cardiovascular tissue regenerative processes represents currently an area of intense research activity. Recent studies have described the potential of exosomes to influence the pathophysiology of immune signaling, tumor metastasis, and angiogenesis. In this review, we briefly discuss progress made in our understanding of the composition and the roles of exosomes in relation to EC regeneration as well as revascularization of ischemic tissues.

Keywords: angiogenesis; endothelial cells; exosomes; regeneration; rejuvenation.

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Figures

FIGURE 1
FIGURE 1
Schematic representation of an exosome and its cargo carrying growth factors, cytokines, and signaling molecules that have been implicated in EC regeneration. PDGFR, platelet derived growth factor receptor; Hsp, heat shock protein; MMP, matrix metalloprotease; SDF, stromal derived factor; HIF, hypoxia inducible factor.
FIGURE 2
FIGURE 2
Schematic representation of a generic exosome and its cargo carrying miRNAs that mediate EC regeneration. Abbreviation: miRNA, microRNA.

References

    1. Abid Hussein M. N., Böing A. N., Sturk A., Hau C. M., Nieuwland R. (2017). Inhibition of microparticle release triggers endothelial cell apoptosis and detachment. Thromb. Haemost. 98 1096–1107. 10.1160/TH05-04-0231 - DOI - PubMed
    1. Adamiak M., Sahoo S. (2018). Exosomes in myocardial repair: advances and challenges in the development of next-generation therapeutics. Mol. Ther. 26 1635–1643. 10.1016/j.ymthe.2018.04.024 - DOI - PMC - PubMed
    1. Adams R. H., Alitalo K. (2007). Molecular regulation of angiogenesis and lymphangiogenesis. Nat. Rev. Mol. Cell Biol. 8 464–478. 10.1038/nrm2183 - DOI - PubMed
    1. Agarwal U., George A., Bhutani S., Ghosh-Choudhary S., Maxwell J. T., Brown M. E., et al. (2017). Experimental, systems, and computational approaches to understanding the MicroRNA-mediated reparative potential of cardiac progenitor cell-derived exosomes from pediatric patients. Circ. Res. 120 701–712. 10.1161/CIRCRESAHA.116.309935 - DOI - PMC - PubMed
    1. Asahara T., Murohara T., Sullivan A., Silver M., van der Zee R., Li T., et al. (1997). Isolation of putative progenitor endothelial cells for angiogenesis. Science 275 964–967. - PubMed

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