Temporal Enzymatic Treatment to Enhance the Remodeling of Multiple Cartilage Microtissues into a Structurally Organized Tissue

Author:

Burdis Ross123ORCID,Gallostra Xavier Barceló123,Kelly Daniel J.1234ORCID

Affiliation:

1. Trinity Centre for Biomedical Engineering Trinity Biomedical Sciences Institute Trinity College Dublin Dublin D02 PN40 Ireland

2. Department of Mechanical Manufacturing and Biomedical Engineering School of Engineering Trinity College Dublin Dublin D02 PN40 Ireland

3. Advanced Materials and Bioengineering Research Centre (AMBER) Royal College of Surgeons in Ireland and Trinity College Dublin Dublin D02 PN40 Ireland

4. Department of Anatomy and Regenerative Medicine Royal College of Surgeons in Ireland Dublin D02 YN77 Ireland

Abstract

AbstractScaffold‐free tissue engineering aims to recapitulate key aspects of normal developmental processes to generate biomimetic grafts. Although functional cartilaginous tissues are engineered using such approaches, considerable challenges remain. Herein, the benefits of engineering cartilage via the fusion of multiple cartilage microtissues compared to using (millions of) individual cells to generate a cartilaginous graft are demonstrated. Key advantages include the generation of a richer extracellular matrix, more hyaline‐like cartilage phenotype, and superior shape fidelity. A major drawback of aggregate engineering is that individual microtissues do not completely (re)model and remnants of their initial architectures remain throughout the macrotissue. To address this, a temporal enzymatic (chondroitinase‐ABC) treatment is implemented to accelerate structural (re)modeling and shown to support robust fusion between adjacent microtissues, enhance microtissue (re)modeling, and enable the development of a more biomimetic tissue with a zonally organized collagen network. Additionally, enzymatic treatment is shown to modulate matrix composition, tissue phenotype, and to a lesser extent, tissue mechanics. This work demonstrates that microtissue self‐organization is an effective method for engineering scaled‐up cartilage grafts with a predefined geometry and near‐native levels of matrix accumulation. Importantly, key limitations associated with using biological building blocks can be alleviated by temporal enzymatic treatment during graft development.

Funder

Science Foundation Ireland

European Regional Development Fund

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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