Abstract

BackgroundDecellularized animal organs have been used as scaffolds for tissue engineering. To make a properly functioning scaffolds, the extracellular matrix (ECM) components must be preserved after decellularization. Because pulsatile flow is known to be beneficial for tissue perfusion, pulsatile perfusion of a detergent might decrease the exposure time of the tissues to the detergent used for decellularization. Using Energy Equivalent Pressure (EEP) as a pulsatility parameter, the effect of pulsatile flow in decellularization process is studied.ResultsTwelve rat hearts were decellularization with 1% sodium dodecyl sulfate (SDS) solution for 2 h. They are divided into two groups, one with pulsatile perfusion (n = 6), the other with non-pulsatile perfusion (n = 6) of SDS. The initial mean perfusion pressures were same in both group. The result indicated that the EEP and the perfusion flow were increased significantly in the pulsatile group compared to the non-pulsatile group. Photographs taken during the decellularization showed more profound decellularization in the pulsatile group. The residual DNA content in the scaffolds was significantly lower in the pulsatile group. However, the level of ECM components, collagen and GAG showed no significant differences between the groups.ConclusionsDecellularization is more efficient in pulsatile flow than in non-pulsatile flow but still preserves the ECM molecules.

Highlights

  • Decellularized animal organs have been used as scaffolds for tissue engineering

  • The Equivalent Pressure (EEP) increased as pulsatile perfusion began in the pulsatile group (101 ± 17 mmHg), while it remained nearly constant in the non-pulsatile group (80 ± 0.3 mmHg)

  • The results of our study show that pulsatile perfusion can reduce decellularization time and preserve extracellular matrix (ECM) structures

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Summary

Introduction

To make a properly functioning scaffolds, the extracellular matrix (ECM) components must be preserved after decellularization. Results: Twelve rat hearts were decellularization with 1% sodium dodecyl sulfate (SDS) solution for 2 h They are divided into two groups, one with pulsatile perfusion (n = 6), the other with non-pulsatile perfusion (n = 6) of SDS. The result indicated that the EEP and the perfusion flow were increased significantly in the pulsatile group compared to the non-pulsatile group. Removing cells from a tissue leaves the extracellular matrix (ECM), which is well tolerated, even by xenogeneic recipients [1]. The detergent breaks down cell membranes, and the intracellular components are freely washed out by the solution, leaving the ECM, which is relatively resistant to detergent extraction.

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