Key result
Bioreactor preconditioning of valve scaffolds seeded with EPC-derived ECs improves anti-thrombotic properties versus unseeded scaffolds.
Why the study?
Calcification and tissue deterioration leading to thromboembolism remain clinical concerns after bioprosthetic heart valve replacement, motivating strategies to prevent thrombosis such as endothelialization.
Does endothelialization using EPC-derived ECs in a pulsatile bioreactor improve the anti-thrombotic properties of decellularized porcine heart valves?
Does endothelialization using EPC-derived ECs in a pulsatile bioreactor improve the anti-thrombotic properties of decellularized porcine heart valves?
Preconditioning endothelial cells on decellularized valve matrices using a pulsatile bioreactor improves anti-thrombotic properties, potentially reducing thrombosis after bioprosthetic valve implantation.
Stepwise bioreactor preconditioning up to 2 L/min supports uniform endothelialization and anti-thrombotic effects in vitro; leaves open in vivo translation.
Although calcification remains as the main clinical concern associated with bioprosthetic heart valve replacement surgery, there is evidence that tissue deterioration leads to thromboembolism. In such instances, measures that prevent thrombosis may be beneficial. To minimize thrombosis, endothelialization of the valve surface before implantation has been proposed to facilitate coverage. In this study we aimed to define the optimal flow parameters for the endothelialization of decellularized heart valves using endothelial progenitor cell (EPC)-derived endothelial cells (ECs). We assessed the thrombogenic characteristics of the endothelialized heart valve surface using a bioreactor. EPC-derived ECs were seeded on decellularized porcine valve scaffolds. A computer-controlled bioreactor system was used to determine the optimal flow rates. Successful endothelialization was achieved by preconditioning the cell-seeded valves with stepwise increases in volume flow rate up to 2 L/min for 7 days. We show that decellularized valve scaffolds seeded with EPC-derived ECs improved the anti-thrombotic properties of the valve, whereas the scaffolds without ECs escalated the coagulation process. This study demonstrates that preconditioning of ECs seeded on valve matrices using a bioreactor system is necessary for achieving uniform endothelialization of valve scaffolds, which may reduce thrombotic activity after implantation in vivo.
No takes yet. Share an insight, caveat, or question.
Lee et al. (2009) studied Bioprosthetic heart valve thrombosis. Endothelialization using EPC-derived ECs preconditioned in a bioreactor vs. Decellularized valve scaffolds without ECs was evaluated on Thrombogenic characteristics. Preconditioning decellularized valve scaffolds seeded with EPC-derived ECs in a bioreactor up to 2 L/min for 7 days improved anti-thrombotic properties compared to scaffolds without ECs.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: