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Optimizing bioink composition for human chondrocyte expression of lubricin

Kari Martyniak, Sean Kennedy, Maria A. Cruz, Makan Karimzadeh, Oju Jeon, Eben Alsberg, View ORCID ProfileThomas J. Kean
doi: https://doi.org/10.1101/2022.11.14.516490
Kari Martyniak
1Biionix Cluster, Internal Medicine, College of Medicine, University of Central Florida, Orlando, FL, United States
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Sean Kennedy
1Biionix Cluster, Internal Medicine, College of Medicine, University of Central Florida, Orlando, FL, United States
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Maria A. Cruz
1Biionix Cluster, Internal Medicine, College of Medicine, University of Central Florida, Orlando, FL, United States
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Makan Karimzadeh
1Biionix Cluster, Internal Medicine, College of Medicine, University of Central Florida, Orlando, FL, United States
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Oju Jeon
2Department of Biomedical Engineering, University of Illinois, Chicago, IL, United States
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Eben Alsberg
2Department of Biomedical Engineering, University of Illinois, Chicago, IL, United States
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Thomas J. Kean
1Biionix Cluster, Internal Medicine, College of Medicine, University of Central Florida, Orlando, FL, United States
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  • ORCID record for Thomas J. Kean
  • For correspondence: Thomas.kean@ucf.edu
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Abstract

The surface zone of articular cartilage is the first area impacted by cartilage defects, commonly resulting in osteoarthritis. Chondrocytes in the surface zone of articular cartilage synthesize and secrete lubricin, a proteoglycan that functions as a lubricant protecting the deeper layers from shear stress. 3D bioprinting is a tissue engineering technique that uses cells encapsulated in biomaterials to fabricate 3D constructs. Gelatin methacrylate (GelMA) is a frequently used biomaterial for 3D bioprinting cartilage. Oxidized methacrylated alginate (OMA) is a chemically modified alginate designed for its tunable degradation rate and mechanical properties. To determine an optimal combination of GelMA and OMA for lubricin expression, we used our novel high-throughput human articular chondrocyte reporter system. Primary human chondrocytes were transduced with PRG4 (lubricin) promoter-driven Gaussia luciferase, allowing for temporal assessment of lubricin expression. A lubricin expression driven Design of Experiment screen and subsequent validation identified 14% GelMA/2% OMA for further study. Therefore, 14% GelMA/2% OMA, 14% GelMA and 16% GelMA were 3D bioprinted. The combination of lubricin protein expression and shape retention over the 22 days in culture, determined the 14% GelMA/2%OMA to be the optimal formulation for lubricin secretion.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted November 16, 2022.
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Optimizing bioink composition for human chondrocyte expression of lubricin
Kari Martyniak, Sean Kennedy, Maria A. Cruz, Makan Karimzadeh, Oju Jeon, Eben Alsberg, Thomas J. Kean
bioRxiv 2022.11.14.516490; doi: https://doi.org/10.1101/2022.11.14.516490
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Optimizing bioink composition for human chondrocyte expression of lubricin
Kari Martyniak, Sean Kennedy, Maria A. Cruz, Makan Karimzadeh, Oju Jeon, Eben Alsberg, Thomas J. Kean
bioRxiv 2022.11.14.516490; doi: https://doi.org/10.1101/2022.11.14.516490

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