Capability of human umbilical cord blood progenitor-derived endothelial cells to form an efficient lining on a polyester vascular graft in vitro

• Published in: Acta biomaterialia 2009-05, Vol.5 (4), p.1147-1157
• Main Authors: Bérard, Xavier, Rémy-Zolghadri, Murielle, Bourget, Chantal, Turner, Neill, Bareille, Reine, Daculsi, Richard, Bordenave, Laurence
• Format: Article
• Language: English
• Subjects: Biocompatibility evaluation; Blood Vessels - cytology; Cell Proliferation; Cells, Cultured; Endothelial Cells - cytology; Endothelial Cells - metabolism; Fetal Blood - cytology; Fetal Blood - metabolism; Gene Expression Regulation; Gene regulation; Hematopoietic Stem Cells - cytology; Hematopoietic Stem Cells - metabolism; Humans; Polyesters; Progenitor-derived endothelial cells; Shear stress; Vascular grafts
• ISSN: 1742-7061; 1878-7568
• DOI: 10.1016/j.actbio.2008.10.002

One of the goals of vascular tissue engineering is to create functional conduits for small-diameter bypass grafting. The present biocompatibility study was undertaken to check the ability of cord blood progenitor-derived endothelial cells (PDECs) to take the place of endothelial cells in vascular tissue engineering. After isolation, culture and characterization of endothelial progenitor cells, the following parameters were explored, with a commercial knitted polyester prosthesis (Polymaille ® C, Laboratoires Pérouse, France) impregnated with collagen: cell adhesion and proliferation, colonization, cell retention on exposure to flow, and the ability of PDECs to be regulated by arterial shear stress via mRNA levels. PDECs were able to adhere to commercial collagen-coated vascular grafts in serum-free conditions, and were maintained but did not proliferate when seeded at 2.0 × 10 5 cm −2. Cellularized conduits were analyzed by histology and histochemical staining, demonstrating collagen impregnation and the endothelial characteristics of the colonizing cells. Thirty-six hours after cell seeding the grafts were maintained for 6 h of either static conditions (controls) or application of pulsatile laminar shear stress, which restored the integrity of the monolayer. Finally, quantitative real-time RT-PCR analysis performed at 4 and 8 h from cells lining grafts showed that MMP1 mRNA only was increased at 4 h whereas vWF, VE-cadherin and KDR were not significantly modified at 4 and 8 h. Our results show that human cord blood PDECs are capable of forming an efficient lining and to withstand shear stress.