Bioprinting of Stem Cell Spheroids Followed by Post‐Printing Chondrogenic Differentiation for Cartilage Tissue Engineering

Author:

Decarli Monize Caiado12,Seijas‐Gamardo Adrián1,Morgan Francis L. C.1,Wieringa Paul1,Baker Matthew B.1,Silva Jorge Vicente L.3,Moraes Ângela Maria2,Moroni Lorenzo1,Mota Carlos1ORCID

Affiliation:

1. MERLN Institute for Technology‐Inspired Regenerative Medicine Department of Complex Tissue Regeneration Maastricht University Universiteitssingel, 40 Maastricht Limburg 6229 ER the Netherlands

2. Department of Engineering of Biomaterials and of Bioprocesses School of Chemical Engineering University of Campinas ‐ UNICAMP Av. Albert Einstein, 500, Cidade Universitária “Zeferino Vaz” Campinas SP 13083‐852 Brazil

3. Three‐Dimensional Technologies Research Group CTI Renato Archer Rodovia Dom Pedro I SP‐65, Km 143,6 ‐ Amarais Campinas SP 13069‐901 Brazil

Abstract

AbstractCartilage tissue presents low self‐repair capability and lesions often undergo irreversible progression. Structures obtained by tissue engineering, such as those based in extrusion bioprinting of constructs loaded with stem cell spheroids may offer valuable alternatives for research and therapeutic purposes. Human mesenchymal stromal cell (hMSC) spheroids can be chondrogenically differentiated faster and more efficiently than single cells. This approach allows obtaining larger tissues in a rapid, controlled and reproducible way. However, it is challenging to control tissue architecture, construct stability, and cell viability during maturation. Herein, this work reports a reproducible bioprinting process followed by a successful post‐bioprinting chondrogenic differentiation procedure using large quantities of hMSC spheroids encapsulated in a xanthan gum‐alginate hydrogel. Multi‐layered constructs are bioprinted, ionically crosslinked, and post chondrogenically differentiated for 28 days. The expression of glycosaminoglycan, collagen II and IV are observed. After 56 days in culture, the bioprinted constructs are still stable and show satisfactory cell metabolic activity with profuse extracellular matrix production. These results show a promising procedure to obtain 3D models for cartilage research and ultimately, an in vitro proof‐of‐concept of their potential use as stable chondral tissue implants.

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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