TY - JOUR
T1 - Tissue engineered in-vitro vascular patch fabrication using hybrid 3D printing and electrospinning
AU - Mayoral, Isabel
AU - Bevilacqua, Elisa
AU - Gómez, Gorka
AU - Hmadcha, Abdelkrim
AU - González-Loscertales, Ignacio
AU - Reina, Esther
AU - Sotelo, Julio
AU - Domínguez, Antonia
AU - Pérez-Alcántara, Pedro
AU - Smani, Younes
AU - González-Puertas, Patricia
AU - Mendez, Ana
AU - Uribe, Sergio
AU - Smani, Tarik
AU - Ordoñez, Antonio
AU - Valverde, Israel
N1 - Funding Information:
This research was funded by Instituto de Salud Carlos III through the projects PI17/01409 , PT20/00069 (Plataforma ISCIII de Biobancos y Biomodelos) and PI20/00467 (Co-funded by European Regional Development Fund/European Social Fund “A way to make Europe"/"Investing in your future”) and by the Foundation ‘Menudos Corazones to help children with heart disease' and the Spanish Society of Paediatric Cardiology and Congenital Heart Disease (SECPCC) , grant number ‘Menudos Corazones 2020’ . This work was also supported by the Spanish Ministry of Economy and Competitiveness ( PID2019-104084GB-C22 ) and ANID – Millennium Science Initiative Program – ICN2021_004 and ANID – Millennium Science Initiative Program – NCN17_129 , ANID FONDECYT de Iniciación en Investigación #11200481 , ANID FONDECYT #1181057 .
Publisher Copyright:
© 2022 The Authors
PY - 2022/3
Y1 - 2022/3
N2 - Three-dimensional (3D) engineered cardiovascular tissues have shown great promise to replace damaged structures. Specifically, tissue engineering vascular grafts (TEVG) have the potential to replace biological and synthetic grafts. We aimed to design an in-vitro patient-specific patch based on a hybrid 3D print combined with vascular smooth muscle cells (VSMC) differentiation. Based on the medical images of a 2 months-old girl with aortic arch hypoplasia and using computational modelling, we evaluated the most hemodynamically efficient aortic patch surgical repair. Using the designed 3D patch geometry, the scaffold was printed using a hybrid fused deposition modelling (FDM) and electrospinning techniques. The scaffold was seeded with multipotent mesenchymal stem cells (MSC) for later maturation to derived VSMC (dVSMC). The graft showed adequate resistance to physiological aortic pressure (burst pressure 101 ± 15 mmHg) and a porosity gradient ranging from 80 to 10 μm allowing cells to infiltrate through the entire thickness of the patch. The bio-scaffolds showed good cell viability at days 4 and 12 and adequate functional vasoactive response to endothelin-1. In summary, we have shown that our method of generating patient-specific patch shows adequate hemodynamic profile, mechanical properties, dVSMC infiltration, viability and functionality. This innovative 3D biotechnology has the potential for broad application in regenerative medicine and potentially in heart disease prevention.
AB - Three-dimensional (3D) engineered cardiovascular tissues have shown great promise to replace damaged structures. Specifically, tissue engineering vascular grafts (TEVG) have the potential to replace biological and synthetic grafts. We aimed to design an in-vitro patient-specific patch based on a hybrid 3D print combined with vascular smooth muscle cells (VSMC) differentiation. Based on the medical images of a 2 months-old girl with aortic arch hypoplasia and using computational modelling, we evaluated the most hemodynamically efficient aortic patch surgical repair. Using the designed 3D patch geometry, the scaffold was printed using a hybrid fused deposition modelling (FDM) and electrospinning techniques. The scaffold was seeded with multipotent mesenchymal stem cells (MSC) for later maturation to derived VSMC (dVSMC). The graft showed adequate resistance to physiological aortic pressure (burst pressure 101 ± 15 mmHg) and a porosity gradient ranging from 80 to 10 μm allowing cells to infiltrate through the entire thickness of the patch. The bio-scaffolds showed good cell viability at days 4 and 12 and adequate functional vasoactive response to endothelin-1. In summary, we have shown that our method of generating patient-specific patch shows adequate hemodynamic profile, mechanical properties, dVSMC infiltration, viability and functionality. This innovative 3D biotechnology has the potential for broad application in regenerative medicine and potentially in heart disease prevention.
KW - 3D printing
KW - Electrospinning
KW - Mesenchymal stem cells
KW - Tissue engineering
KW - Vascular graft
UR - https://www.scopus.com/pages/publications/85129054892
U2 - 10.1016/j.mtbio.2022.100252
DO - 10.1016/j.mtbio.2022.100252
M3 - Article
C2 - 35509864
AN - SCOPUS:85129054892
SN - 2590-0064
VL - 14
JO - Materials Today Bio
JF - Materials Today Bio
M1 - 100252
ER -