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Method for manufacture and cryopreservation of cartilage microtissues.

Authors :
Shajib MS
Futrega K
Franco RAG
McKenna E
Guillesser B
Klein TJ
Crawford RW
Doran MR
Source :
Journal of tissue engineering [J Tissue Eng] 2023 Jul 26; Vol. 14, pp. 20417314231176901. Date of Electronic Publication: 2023 Jul 26 (Print Publication: 2023).
Publication Year :
2023

Abstract

The financial viability of a cell and tissue-engineered therapy may depend on the compatibility of the therapy with mass production and cryopreservation. Herein, we developed a method for the mass production and cryopreservation of 3D cartilage microtissues. Cartilage microtissues were assembled from either 5000 human bone marrow-derived stromal cells (BMSC) or 5000 human articular chondrocytes (ACh) each using a customized microwell platform (the Microwell-mesh). Microtissues rapidly accumulate homogenous cartilage-like extracellular matrix (ECM), making them potentially useful building blocks for cartilage defect repair. Cartilage microtissues were cultured for 5 or 10 days and then cryopreserved in 90% serum plus 10% dimethylsulfoxide (DMSO) or commercial serum-free cryopreservation media. Cell viability was maximized during thawing by incremental dilution of serum to reduce oncotic shock, followed by washing and further culture in serum-free medium. When assessed with live/dead viability dyes, thawed microtissues demonstrated high viability but reduced immediate metabolic activity relative to unfrozen control microtissues. To further assess the functionality of the freeze-thawed microtissues, their capacity to amalgamate into a continuous tissue was assess over a 14 day culture. The amalgamation of microtissues cultured for 5 days was superior to those that had been cultured for 10 days. Critically, the capacity of cryopreserved microtissues to amalgamate into a continuous tissue in a subsequent 14-day culture was not compromised, suggesting that cryopreserved microtissues could amalgamate within a cartilage defect site. The quality ECM was superior when amalgamation was performed in a 2% O <subscript>2</subscript> atmosphere than a 20% O <subscript>2</subscript> atmosphere, suggesting that this process may benefit from the limited oxygen microenvironment within a joint. In summary, cryopreservation of cartilage microtissues is a viable option, and this manipulation can be performed without compromising tissue function.<br />Competing Interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: MRD and KF founded a company that seeks to commercialize the Microwell-mesh.<br /> (© The Author(s) 2023.)

Details

Language :
English
ISSN :
2041-7314
Volume :
14
Database :
MEDLINE
Journal :
Journal of tissue engineering
Publication Type :
Academic Journal
Accession number :
37529249
Full Text :
https://doi.org/10.1177/20417314231176901