Spatial patterning of phenotypically distinct microtissues to engineer osteochondral grafts for biological joint resurfacing. (October 2022)

• Record Type: Journal Article
• Authors: Burdis, Ross; Chariyev-Prinz, Farhad; Browe, David C.; Freeman, Fiona E.; Nulty, Jessica; McDonnell, Emily E.; Eichholz, Kian F.; Wang, Bin; Brama, Pieter; Kelly, Daniel J.
• Is Part Of: Biomaterials. Volume 289(2022)
• Publication Date: 2022-10
• Subjects: Osteochondral -- Developmental engineering -- Microtissues -- Modular biofabrication -- Self-organisation; Biomedical materials -- Periodicals; Biocompatible Materials -- Periodicals; Biomatériaux -- Périodiques; 610.28
• DOI: 10.1016/j.biomaterials.2022.121750
• Languages: English
• ISSNs: 0142-9612

Abstract

Abstract: Modular biofabrication strategies using microtissues or organoids as biological building blocks have great potential for engineering replacement tissues and organs at scale. Here we describe the development of a biofabrication strategy to engineer osteochondral tissues by spatially localising phenotypically distinct cartilage microtissues within an instructive 3D printed polymer framework. We first demonstrate that immature cartilage microtissues can spontaneously fuse to form homogeneous macrotissues, and that combining less cellular microtissues results in superior fusion and the generation of a more hyaline-like cartilage containing higher levels of sulphated glycosaminoglycans and type II collagen. Furthermore, temporally exposing developing microtissues to transforming growth factor-β accelerates their volumetric growth and subsequent capacity to fuse into larger hyaline cartilage grafts. Next, 3D printed polymeric frameworks are used to further guide microtissue fusion and the subsequent self-organisation process, resulting in the development of a macroscale tissue with zonal collagen organisation analogous to the structure seen in native articular cartilage. To engineer osteochondral grafts, hypertrophic cartilage microtissues are engineered as bone precursor tissues and spatially localised below phenotypically stable cartilage microtissues. Implantation of these engineered grafts into critically-sized caprine osteochondral defects results in effective defect stabilisation and histologically supports the restoration of a more normal articular surface after 6 months in vivo . These findings support the use of such modular biofabrication strategies for biological joint resurfacing.