McMurtrey Richard J
1 Institute of Neural Regeneration & Tissue Engineering , Highland, Utah, United States .
2 Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford , Oxford, United Kingdom .
Tissue Eng Part C Methods. 2016 Mar;22(3):221-49. doi: 10.1089/ten.TEC.2015.0375. Epub 2016 Jan 21.
Diffusion models are important in tissue engineering as they enable an understanding of gas, nutrient, and signaling molecule delivery to cells in cell cultures and tissue constructs. As three-dimensional (3D) tissue constructs become larger, more intricate, and more clinically applicable, it will be essential to understand internal dynamics and signaling molecule concentrations throughout the tissue and whether cells are receiving appropriate nutrient delivery. Diffusion characteristics present a significant limitation in many engineered tissues, particularly for avascular tissues and for cells whose viability, differentiation, or function are affected by concentrations of oxygen and nutrients. This article seeks to provide novel analytic solutions for certain cases of steady-state and nonsteady-state diffusion and metabolism in basic 3D construct designs (planar, cylindrical, and spherical forms), solutions that would otherwise require mathematical approximations achieved through numerical methods. This model is applied to cerebral organoids, where it is shown that limitations in diffusion and organoid size can be partially overcome by localizing metabolically active cells to an outer layer in a sphere, a regionalization process that is known to occur through neuroglial precursor migration both in organoids and in early brain development. The given prototypical solutions include a review of metabolic information for many cell types and can be broadly applied to many forms of tissue constructs. This work enables researchers to model oxygen and nutrient delivery to cells, predict cell viability, study dynamics of mass transport in 3D tissue constructs, design constructs with improved diffusion capabilities, and accurately control molecular concentrations in tissue constructs that may be used in studying models of development and disease or for conditioning cells to enhance survival after insults like ischemia or implantation into the body, thereby providing a framework for better understanding and exploring the characteristics and behaviors of engineered tissue constructs.
扩散模型在组织工程中很重要,因为它们有助于理解气体、营养物质和信号分子在细胞培养物和组织构建体中向细胞的传递。随着三维(3D)组织构建体变得更大、更复杂且更具临床适用性,了解整个组织的内部动态、信号分子浓度以及细胞是否获得适当的营养物质传递将至关重要。扩散特性在许多工程组织中构成了重大限制,特别是对于无血管组织以及其活力、分化或功能受氧气和营养物质浓度影响的细胞。本文旨在为基本3D构建体设计(平面、圆柱和球形形式)中的某些稳态和非稳态扩散及代谢情况提供新颖的解析解,这些解若通过数值方法实现则需要数学近似。该模型应用于脑类器官,结果表明通过将代谢活跃细胞定位在球体的外层,可以部分克服扩散和类器官大小的限制,这种区域化过程已知在类器官和早期脑发育中通过神经胶质前体细胞迁移发生。给出的典型解包括对许多细胞类型代谢信息的综述,可广泛应用于多种形式的组织构建体。这项工作使研究人员能够模拟氧气和营养物质向细胞的传递、预测细胞活力、研究3D组织构建体中的质量传输动态、设计具有改善扩散能力的构建体以及精确控制组织构建体中的分子浓度,这些构建体可用于研究发育和疾病模型或使细胞适应以提高缺血或植入体内等损伤后的存活率,从而为更好地理解和探索工程组织构建体的特性和行为提供了一个框架。