Dudman, J.; Ferreira, A.M.; Gentile, P.; Wang, X.; Dalgarno, K. Microvalve Bioprinting of MSC-Chondrocyte Co-Cultures. Cells2021, 10, 3329.
Dudman, J.; Ferreira, A.M.; Gentile, P.; Wang, X.; Dalgarno, K. Microvalve Bioprinting of MSC-Chondrocyte Co-Cultures. Cells 2021, 10, 3329.
Dudman, J.; Ferreira, A.M.; Gentile, P.; Wang, X.; Dalgarno, K. Microvalve Bioprinting of MSC-Chondrocyte Co-Cultures. Cells2021, 10, 3329.
Dudman, J.; Ferreira, A.M.; Gentile, P.; Wang, X.; Dalgarno, K. Microvalve Bioprinting of MSC-Chondrocyte Co-Cultures. Cells 2021, 10, 3329.
Abstract
Recent improvements within the fields of high-throughput screening and 3D tissue culture have provided the possibility of developing in vitro micro-tissue models that can be used to study diseases and screen potential new therapies. This paper reports a proof of concept study on the use of microvalve-based bioprinting to create laminar MSC-chondrocyte co-cultures as an in vitro model of autologous chondrocyte implantation (ACI), an established cellular therapy for osteoarthritis. Microvalve-based bioprinting uses microvalves to deposit cells suspended in a liquid in a consistent and repeatable manner. In this case MSCs and chondrocytes have been sequentially deposited into an insert based transwell system in order to create a laminar co-culture, with variations in the ratios of the cell types used to investigate the potential for MSCs to stimulate improved repair. Histological and indirect immunofluorescence staining revealed the formation of dense tissue structures within the chondrocyte and MSC-chondrocyte cell co-cultures, alongside the establishment of a proliferative region at the base of the tissue. No stimulatory or inhibitory effect in terms of ECM production was observed through the introduction of MSCs, although the potential for an immunomodulatory benefit remains. This proof-of-concept study therefore provides a novel method to enable the scalable production of therapeutically relevant micro-tissue models that can be used for in vitro research to optimise ACI procedures.
Biology and Life Sciences, Cell and Developmental Biology
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