Tissue Eng Regen Med.  2023 Aug;20(5):695-704. 10.1007/s13770-023-00546-9.

Platelet-Derived Growth Factor-BB Priming Enhances Vasculogenic Capacity of Bone Marrow-Derived Endothelial Precursor Like Cells

Affiliations
  • 1Department of Genetic Engineering, College of Life Science and Graduate School of Biotechnology, Kyung Hee University, Yongin 17104, South Korea
  • 2Department of Biomedical Science and Technology, Graduated School, Kyung Hee University, Seoul, Korea
  • 3KHU Institute of Regenerative Medicine, KHU Hospital, Seoul, Korea
  • 4Elphis Cell Therapeutics Inc, Yongin, Korea

Abstract

BACKGROUND
Human endothelial progenitor cells (EPCs) were first identified in the peripheral blood and later in the cord blood and bone marrow (BM) with different vascularization capacity and different surface marker profiles. However, their identity and functional roles in neovascularization have not been clearly demonstrated in vivo and in vitro.
METHODS
Characterization of BM-EPC like cells were performed by fluorescence-activated cell sorting, immunofluorescence staining, enzyme-linked immunosorbent assay, Matrigel tube formation assay, and western blot analysis.
RESULTS
BM-EPC like cells were identified by selective adhesion to fibronectin and collagen from BM mononuclear cells, which generate fast-growing colonies with spindle morphology, express surface markers of CD105, vWF, UEA-I lectin binding, secrete HGF, VEGF, TGF-beta1 but can be distinguished from circulating EPC and endothelial cells by no expression of surface markers such as CD31, CD309, CD45, and CD34. These BM-EPC like cells shared many cell surface markers of BM-mesenchymal stem cells (MSC) but also can be distinguished by their vasculogenic property and other unique surface markers. Furthermore, the vasculogenic capacity of BM-EPC like cells were enhanced by co-culture of BMMSC or PDGF-BB priming. PDGF-BB stimulated cell migration, proliferation, and secretion of laminin b-1, which was proposed as one of the mechanisms involved in the better vascularization of BM-EPC like cells.
CONCLUSION
PDGF-BB priming may be applied to improve the potency and function of BM-EPC like cells as vasculogenic cell therapy for the ischemic vascular repair.

Keyword

EPC; Angiogenesis; PDGF-BB; PDGF receptor; Vasculogenesis
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