Abstract

Successful osteochondral defect repair requires regenerating the subchondral bone whilst simultaneously promoting the development of an overlying layer of articular cartilage that is resistant to vascularization and endochondral ossification. During skeletal development articular cartilage also functions as a surface growth plate, which postnatally is replaced by a more spatially complex bone-cartilage interface. Motivated by this developmental process, the hypothesis of this study is that bi-phasic, fibre-reinforced cartilaginous templates can regenerate both the articular cartilage and subchondral bone within osteochondral defects created in caprine joints. To engineer mechanically competent implants, we first compared a range of 3D printed fibre networks (PCL, PLA and PLGA) for their capacity to mechanically reinforce alginate hydrogels whilst simultaneously supporting mesenchymal stem cell (MSC) chondrogenesis in vitro. These mechanically reinforced, MSC-laden alginate hydrogels were then used to engineer the endochondral bone forming phase of bi-phasic osteochondral constructs, with the overlying chondral phase consisting of cartilage tissue engineered using a co-culture of infrapatellar fat pad derived stem/stromal cells (FPSCs) and chondrocytes. Following chondrogenic priming and subcutaneous implantation in nude mice, these bi-phasic cartilaginous constructs were found to support the development of vascularised endochondral bone overlaid by phenotypically stable cartilage. These fibre-reinforced, bi-phasic cartilaginous templates were then evaluated in clinically relevant, large animal (caprine) model of osteochondral defect repair. Although the quality of repair was variable from animal-to-animal, in general more hyaline-like cartilage repair was observed after 6 months in animals treated with bi-phasic constructs compared to animals treated with commercial control scaffolds. This variability in the quality of repair points to the need for further improvements in the design of 3D bioprinted implants for joint regeneration. Statement of SignificanceSuccessful osteochondral defect repair requires regenerating the subchondral bone whilst simultaneously promoting the development of an overlying layer of articular cartilage. In this study, we hypothesised that bi-phasic, fibre-reinforced cartilaginous templates could be leveraged to regenerate both the articular cartilage and subchondral bone within osteochondral defects. To this end we used 3D printed fibre networks to mechanically reinforce engineered transient cartilage, which also contained an overlying layer of phenotypically stable cartilage engineered using a co-culture of chondrocytes and stem cells. When chondrogenically primed and implanted into caprine osteochondral defects, these fibre-reinforced bi-phasic cartilaginous grafts were shown to spatially direct tissue development during joint repair. Such developmentally inspired tissue engineering strategies, enabled by advances in biofabrication and 3D printing, could form the basis of new classes of regenerative implants in orthopaedic medicine.

Highlights

  • Treating osteochondral (OC) defects requires supporting subchondral bone repair whilst simultaneously regenerating articular cartilage that is resistant to vascularisation and endochondral ossification

  • The ‘chondral’ region of these engineered tissues consisted of a co-culture of mesenchymal stem cells (MSCs) and chondrocytes, which we and others have shown can promote the development of a cartilage tissue resistant to hypertrophy and mineralisation [19,26,27,28], while the osseous region was generated using bone marrow MSC-laden hydrogels primed for chondrogenesis and endochondral ossification

  • The overall aim of this study was to engineer fibre-reinforced cartilage templates for osteochondral defect repair, whereby the osseous region of the implant is designed to undergo endochondral ossification, whilst the overlying chondral layer is designed to support the development of stable hyaline cartilage

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Summary

Introduction

Treating osteochondral (OC) defects requires supporting subchondral bone repair whilst simultaneously regenerating articular cartilage that is resistant to vascularisation and endochondral ossification. The ‘chondral’ region of these engineered tissues consisted of a co-culture of mesenchymal stem cells (MSCs) and chondrocytes, which we and others have shown can promote the development of a cartilage tissue resistant to hypertrophy and mineralisation [19,26,27,28], while the osseous region was generated using bone marrow MSC-laden hydrogels primed for chondrogenesis and endochondral ossification This proof-of-principle study was performed in a subcutaneous environment and, the engineered constructs were not subjected to the high levels of mechanical load they will experience upon implantation into a damaged or diseased joint. New biofabrication strategies are required to develop mechanically reinforced hydrogels that have bulk mechanical properties compatible with implantation into load bearing defects, but which provides a cellular environment compatible with differentiation and matrix synthesis

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