Annals of biomedical engineering · 2026
Generation of Fibrin-Based Aortic Vessels with Layer-Specific Cell Architecture Under Pulsatile Perfusion in a Clinical Organ Care System.
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Käding Celina Delia, Glomb Clara-Sophie, Stadler Patrick, Becker Imke, Klingenberg Melanie, Höffler Hans-Klaus, Pflaum Michael, Ruhparwar Arjang, Wilhelmi Mathias, Helms Florian
Аннотация
PURPOSE: Overcoming the limitations of synthetic vascular grafts in the development of biocompatible and regenerative vessels remains a long-term objective in tissue engineering. In this study, we engineered large-diameter fibrin-based vascular grafts with a target inner diameter of 21 mm replicating all three layers of the native human vessel wall in vitro.
METHODS: The Tunica media was reconstructed using a compressed high-density (25 mg/mL) fibrin matrix seeded with smooth muscle cells expressing α-SMA and calponin, differentiated from adipose-derived mesenchymal stem cells (ASCs). The Adventitia-equivalent was formed in a 5 mg/mL fibrin gel containing ASCs, human umbilical vein endothelial cells (HUVECs), and normal human dermal fibroblasts (NHDFs) to enable the formation of a capillary-like network resembling the native adventitial Vasa vasorum. The luminal surface was endothelialized with HUVECs to replicate the Tunica intima. While controls were cultured statically for 7 days, other grafts were evaluated under pulsatile perfusion at physiological pressures using the TransMedics® "Organ Care System Heart™".
RESULTS: The stepwise fabrication technique resulted in three-layered bioartificial vessel equivalents with a mean inner diameter of 21 mm. All constructed vessels (n = 3) maintained sufficient biomechanical stability to withstand physiological pressure (120.9 ± 1.2 to 61.4 ± 12.5 mmHg) at 60 bpm throughout the perfusion period. The aortic grafts exhibited a cyclic stretch (8.95 ± 2.03%) within the physiological range of native vessels. Mechanical stimulation induced a layer-specific physiological cell morphology and alignment across all three layers of the vascular wall. Endothelial coverage was high on static grafts (81.39 ± 2.37%) and on one of three dynamic grafts. Shear stress during perfusion (0.38 ± 0.03 dyn cm-2) remained below physiological levels, and further evaluation under prolonged perfusion (> 21 days) is required to assess long-term biomechanical stability and vascular functionality.
CONCLUSION: This approach may be considered a proof of concept and constitutes a first step toward the development of biometric and functional large-diameter vessel replacements.
METHODS: The Tunica media was reconstructed using a compressed high-density (25 mg/mL) fibrin matrix seeded with smooth muscle cells expressing α-SMA and calponin, differentiated from adipose-derived mesenchymal stem cells (ASCs). The Adventitia-equivalent was formed in a 5 mg/mL fibrin gel containing ASCs, human umbilical vein endothelial cells (HUVECs), and normal human dermal fibroblasts (NHDFs) to enable the formation of a capillary-like network resembling the native adventitial Vasa vasorum. The luminal surface was endothelialized with HUVECs to replicate the Tunica intima. While controls were cultured statically for 7 days, other grafts were evaluated under pulsatile perfusion at physiological pressures using the TransMedics® "Organ Care System Heart™".
RESULTS: The stepwise fabrication technique resulted in three-layered bioartificial vessel equivalents with a mean inner diameter of 21 mm. All constructed vessels (n = 3) maintained sufficient biomechanical stability to withstand physiological pressure (120.9 ± 1.2 to 61.4 ± 12.5 mmHg) at 60 bpm throughout the perfusion period. The aortic grafts exhibited a cyclic stretch (8.95 ± 2.03%) within the physiological range of native vessels. Mechanical stimulation induced a layer-specific physiological cell morphology and alignment across all three layers of the vascular wall. Endothelial coverage was high on static grafts (81.39 ± 2.37%) and on one of three dynamic grafts. Shear stress during perfusion (0.38 ± 0.03 dyn cm-2) remained below physiological levels, and further evaluation under prolonged perfusion (> 21 days) is required to assess long-term biomechanical stability and vascular functionality.
CONCLUSION: This approach may be considered a proof of concept and constitutes a first step toward the development of biometric and functional large-diameter vessel replacements.