Biofabrication of cell-free dual drug-releasing biomimetic scaffolds for meniscal regeneration

• Published in: Biofabrication 2022-01, Vol.14 (1), p.15001
• Main Authors: Hao, Li, Tianyuan, Zhao, Zhen, Yang, Fuyang, Cao, Jiang, Wu, Zineng, Yan, Zhengang, Ding, Shuyun, Liu, Chunxiang, Hao, Zhiguo, Yuan, Quanyi, Guo
• Format: Article
• Language: English
• Subjects: 3D printing; Animals; Becaplermin - pharmacology; biofabrication; Biomimetics; KGN; meniscal regeneration; Meniscus; PDGF-BB; Printing, Three-Dimensional; Rabbits; Regeneration; Tissue Engineering - methods; Tissue Scaffolds
• ISSN: 1758-5082; 1758-5090
• DOI: 10.1088/1758-5090/ac2cd7

Regenerating the meniscus remains challenging because of its avascular, aneural, and alymphatic nature. Three-dimensional (3D) printing technology provides a promising strategy to fabricate biomimetic meniscal scaffolds with an anisotropic architecture, a proper biomechanical microenvironment, and bioactive components. Herein, 3D printing technology is adopted by coencapsulating chemokines (platelet-derived growth factor-BB, PDGF-BB) and small chondroinductive molecules (kartogenin, KGN) within biomimetic polycaprolactone/hydrogel composite scaffolds. The incorporated PDGF-BB is expected to promote endogenous stem cell homing, and KGN in poly(lactic-co-glycolic) acid microspheres is employed to target the chondrogenesis of resident mesenchymal stem cells (MSCs). First, we chose basic bioinks composed of gelatin methacrylamide and hyaluronic acid methacrylate and then incorporated four concentrations (0%, 0.5%, 1.0%, and 2.0%) of meniscal extracellular matrix into the bioink to systematically study the superiority of these combinations and identify the optimally printable bioink. Next, we investigated the scaffold morphology and drug release profile. The effects of releasing the drugs in a sequentially controlled manner from the composite scaffolds on the fate of MSCs were also evaluated. The biofabricated scaffolds, with and without dual drug loading, were further studied in a rabbit model established with a critical-size medial meniscectomy. We found that meniscal scaffolds containing both drugs had combinational advantages in enhancing cell migration and synergistically promoted MSC chondrogenic differentiation. The dual drug-loaded scaffolds also significantly promoted neomeniscal regeneration three and six months after implantation in terms of histological and immunological phenotypes. The results presented herein reveal that this 3D-printed dual drug-releasing meniscal scaffold possesses the potential to act as an off-the-shelf product for the clinical treatment of meniscal injury and related joint degenerative diseases.