A Heuristic Computational Model of Basic Cellular Processes and Oxygenation during Spheroid-Dependent Biofabrication

dc.contributor.authorSego, T. J.
dc.contributor.authorKasacheuski, Uladzimir
dc.contributor.authorHauersperger, Daniel
dc.contributor.authorTovar, Andres
dc.contributor.authorMoldovan, Nicanor I.
dc.contributor.departmentBiomedical Engineering, School of Engineering and Technologyen_US
dc.date.accessioned2018-02-28T15:36:08Z
dc.date.available2018-02-28T15:36:08Z
dc.date.issued2017
dc.description.abstractAn emerging approach in biofabrication is the creation of 3D tissue constructs through scaffold-free, cell spheroid-only methods. The basic mechanism in this technology is spheroid fusion, which is driven by the minimization of energy, the same biophysical mechanism that governs spheroid formation. However, other factors such as oxygen and metabolite accessibility within spheroids impact on spheroid properties and their ability to form larger-scale structures. The goal of our work is to develop a simulation platform eventually capable of predicting the conditions that minimize metabolism-related cell loss within spheroids. To describe the behavior and dynamic properties of the cells in response to their neighbors and to transient nutrient concentration fields, we developed a hybrid discrete-continuous heuristic model, combining a cellular Potts-type approach with field equations applied to a randomly populated spheroid cross-section of prescribed cell-type constituency. This model allows for the description of: (i) cellular adhesiveness and motility; (ii) interactions with concentration fields, including diffusivity and oxygen consumption; and (iii) concentration-dependent, stochastic cell dynamics, driven by metabolite-dependent cell death. Our model readily captured the basic steps of spheroid-based biofabrication (as specifically dedicated to scaffold-free bioprinting), including intra-spheroid cell sorting (both in 2D and 3D implementations), spheroid defect closure, and inter-spheroid fusion. Moreover, we found that when hypoxia occurring at the core of the spheroid was set to trigger cell death, this was amplified upon spheroid fusion, but could be mitigated by external oxygen supplementation. In conclusion, optimization and further development of scaffold-free bioprinting techniques could benefit from our computational model which is able to simultaneously account for both cellular dynamics and metabolism in constructs obtained by scaffold-free biofabrication.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationSego, T. J., Kasacheuski, U., Hauersperger, D., Tovar, A., & Moldovan, N. I. (2017). A heuristic computational model of basic cellular processes and oxygenation during spheroid-dependent biofabrication. Biofabrication, 9(2), 024104. https://doi.org/10.1088/1758-5090/aa6ed4en_US
dc.identifier.urihttps://hdl.handle.net/1805/15303
dc.language.isoenen_US
dc.publisherIOPen_US
dc.relation.isversionof10.1088/1758-5090/aa6ed4en_US
dc.relation.journalBiofabricationen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectbiofabricationen_US
dc.subjectoxygenationen_US
dc.subjectspheroid-dependenten_US
dc.titleA Heuristic Computational Model of Basic Cellular Processes and Oxygenation during Spheroid-Dependent Biofabricationen_US
dc.typeArticleen_US
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