Biofabrication of a shape-stable auricular structure for the reconstruction of ear deformities
Otto, I A; Capendale, P E; Garcia, J P; de Ruijter, M; van Doremalen, R F M; Castilho, M; Lawson, T; Grinstaff, M W; Breugem, C C; Kon, M; Levato, R; Malda, J
(2021) Materials Today Bio, volume 9, pp. 1 - 11
(Article)
Abstract
Bioengineering of the human auricle remains a significant challenge, where the complex and unique shape, the generation of high-quality neocartilage, and shape preservation are key factors. Future regenerative medicine-based approaches for auricular cartilage reconstruction will benefit from a smart combination of various strategies. Our approach to fabrication of an ear-shaped
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construct uses hybrid bioprinting techniques, a recently identified progenitor cell population, previously validated biomaterials, and a smart scaffold design. Specifically, we generated a 3D-printed polycaprolactone (PCL) scaffold via fused deposition modeling, photocrosslinked a human auricular cartilage progenitor cell-laden gelatin methacryloyl (gelMA) hydrogel within the scaffold, and cultured the bioengineered structure in vitro in chondrogenic media for 30 days. Our results show that the fabrication process maintains the viability and chondrogenic phenotype of the cells, that the compressive properties of the combined PCL and gelMA hybrid auricular constructs are similar to native auricular cartilage, and that biofabricated hybrid auricular structures exhibit excellent shape fidelity compared with the 3D digital model along with deposition of cartilage-like matrix in both peripheral and central areas of the auricular structure. Our strategy affords an anatomically enhanced auricular structure with appropriate mechanical properties, ensures adequate preservation of the auricular shape during a dynamic in vitro culture period, and enables chondrogenically potent progenitor cells to produce abundant cartilage-like matrix throughout the auricular construct. The combination of smart scaffold design with 3D bioprinting and cartilage progenitor cells holds promise for the development of clinically translatable regenerative medicine strategies for auricular reconstruction.
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Keywords: Auricular cartilage, Bioprinting, Cartilage progenitor cells, Mechanical reinforcement, Shape preservation, Biomaterials, Biomedical Engineering, Cell Biology, Molecular Biology, Bioengineering, Biotechnology
ISSN: 2590-0064
Publisher: Elsevier BV
Note: Funding Information: The authors declare that there is no conflict of interest. The research was supported by the Netherlands Organization for Scientific Research (Graduate Program Grant 022.005.018 ), the Dutch Arthritis Foundation ( CO-14-001 , LLP-12 and LLP-22 ), and the European Research Council under grant agreement No. 647426 (3D-JOINT). The authors would like to thank prof. R.L.A.W. Bleys and S. Plomp of the Department of Anatomy and dr. L.N.A. van Adrichem of the Department of Plastic, Reconstructive and Hand Surgery of the University Medical Center Utrecht for kindly providing tissues from deceased donors and otoplasty remnants, respectively. The authors kindly acknowledge Mattie van Rijen for helping with histology. The authors thank Nasim Golafshan for drawing the elements of the graphical abstract. The antibody against collagen type II, developed by T.F. Linsenmayer, was obtained from the Developmental Studies Hybridoma Bank, created by the NICHD and maintained at The University of Iowa, Department of Biology, Iowa City, IA 52242, USA. Funding Information: The authors declare that there is no conflict of interest. The research was supported by the Netherlands Organization for Scientific Research (Graduate Program Grant 022.005.018), the Dutch Arthritis Foundation (CO-14-001, LLP-12 and LLP-22), and the European Research Council under grant agreement No. 647426 (3D-JOINT). The authors would like to thank prof. R.L.A.W. Bleys and S. Plomp of the Department of Anatomy and dr. L.N.A. van Adrichem of the Department of Plastic, Reconstructive and Hand Surgery of the University Medical Center Utrecht for kindly providing tissues from deceased donors and otoplasty remnants, respectively. The authors kindly acknowledge Mattie van Rijen for helping with histology. The authors thank Nasim Golafshan for drawing the elements of the graphical abstract. The antibody against collagen type II, developed by T.F. Linsenmayer, was obtained from the Developmental Studies Hybridoma Bank, created by the NICHD and maintained at The University of Iowa, Department of Biology, Iowa City, IA 52242, USA. Publisher Copyright: © 2021 The Author(s)
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