4.3 Article

Ex Vivo Maturation of 3D-Printed, Chondrocyte-Laden, Polycaprolactone-Based Scaffolds Prior to Transplantation Improves Engineered Cartilage Substitute Properties and Integration

Journal

CARTILAGE
Volume 13, Issue 4, Pages 105-118

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/19476035221127638

Keywords

3D bioprinting; additive manufacturing; cartilage; chondrogenic differentiation; scaffold maturation

Categories

Funding

  1. Instituto de Salud Carlos III (ISCIII) [PI16/01430, PI19/01621, PT20/00030]
  2. European Union (EU)
  3. Department of Health [17BU207, 19BU203, 20BU206, 20BU210, 2020111004, 21BU203]
  4. Department of Economy and Competitiveness of the Basque Government [KK-2020/00010, KK-2019/00006, KK-2019/00093]
  5. Diputacion Foral de Gipuzkoa
  6. ISCIII Platform Biobanks and Biomodels [PT20/00030]
  7. EU

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In this study, the in vitro maturation of 3D-printed cell-laden polycaprolactone (PCL) scaffolds was improved, and their in vivo performance was tested in a rabbit auricular cartilage model. The results showed that scaffolds matured in vitro under prochondrogenic hypoxic conditions exhibited better mechanical properties and patterns of cartilage matrix deposition. This suggests that in vitro maturation can improve the functional properties of tissue-engineered grafts.
Objective The surgical management of nasal septal defects due to perforations, malformations, congenital cartilage absence, traumatic defects, or tumors would benefit from availability of optimally matured septal cartilage substitutes. Here, we aimed to improve in vitro maturation of 3-dimensional (3D)-printed, cell-laden polycaprolactone (PCL)-based scaffolds and test their in vivo performance in a rabbit auricular cartilage model. Design Rabbit auricular chondrocytes were isolated, cultured, and seeded on 3D-printed PCL scaffolds. The scaffolds were cultured for 21 days in vitro under standard culture media and normoxia or in prochondrogenic and hypoxia conditions, respectively. Cell-laden scaffolds (as well as acellular controls) were implanted into perichondrium pockets of New Zealand white rabbit ears (N = 5 per group) and followed up for 12 weeks. At study end point, the tissue-engineered scaffolds were extracted and tested by histological, immunohistochemical, mechanical, and biochemical assays. Results Scaffolds previously matured in vitro under prochondrogenic hypoxic conditions showed superior mechanical properties as well as improved patterns of cartilage matrix deposition, chondrogenic gene expression (COL1A1, COL2A1, ACAN, SOX9, COL10A1), and proteoglycan production in vivo, compared with scaffolds cultured in standard conditions. Conclusions In vitro maturation of engineered cartilage scaffolds under prochondrogenic conditions that better mimic the in vivo environment may be beneficial to improve functional properties of the engineered grafts. The proposed maturation strategy may also be of use for other tissue-engineered constructs and may ultimately impact survival and integration of the grafts in the damaged tissue microenvironment.

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