Published June 1, 2017 | Version v1
Journal article

A heuristic computational model of basic cellular processes and oxygenation during spheroid-dependent biofabrication

  • 1. Department of Mechanical Engineering, Indiana University-Purdue University at Indianapolis, IN, United States of America (United States)
  • 2. Department of Computer and Information Science, Indiana University-Purdue University at Indianapolis, IN, United States of America (United States)
  • 3. Department of Biomedical Engineering, Indiana University-Purdue University at Indianapolis, IN, United States of America (United States)

Description

An 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. (paper)

Availability note (English)

Available from http://dx.doi.org/10.1088/1758-5090/aa6ed4

Additional details

Identifiers

Publishing Information

Journal Title
Biofabrication (Online)
Journal Volume
9
Journal Issue
2
Journal Page Range
[12 p.]
ISSN
1758-5090

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
49063139
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ABUNDANCE; ADHESIVES; ANIMAL TISSUES; ANOXIA; APOPTOSIS; CONCENTRATION RATIO; CROSS SECTIONS; FIELD EQUATIONS; METABOLISM; METABOLITES; MINIMIZATION; NUTRIENTS; RANDOMNESS; SIMULATION; SPHEROIDS; STOCHASTIC PROCESSES
Descriptors DEC
BODY; DIMENSIONLESS NUMBERS; EQUATIONS; OPTIMIZATION