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Microfluidic-driven viral infection on cell cultures: Theoretical and experimental study

机译:细胞培养上的微流控病毒感染:理论和实验研究

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摘要

Advanced cell culture systems creating a controlled and predictable microenvironment together with computational modeling may be useful tools to optimize the efficiency of cell infections. In this paper, we will present a phenomenological study of a virus-host infection system, and the development of a multilayered microfluidic platform used to accurately tune the virus delivery from a diffusive-limited regime to a convective-dominated regime. Mathematical models predicted the convective-diffusive regimes developed within the system itself and determined the dominating mass transport phenomena. Adenoviral vectors carrying the enhanced green fluorescent protein (EGFP) transgene were used at different multiplicities of infection (MOI) to infect multiple cell types, both in standard static and in perfused conditions. Our results validate the mathematical models and demonstrate how the infection processes through perfusion via microfluidic platform led to an enhancement of adenoviral infection efficiency even at low MOIs. This was particularly evident at the longer time points, since the establishment of steady-state condition guaranteed a constant viral concentration close to cells, thus strengthening the efficiency of infection. Finally, we introduced the concept of effective MOI, a more appropriate variable for microfluidic infections that considers the number of adenoviruses in solution per cell at a certain time.
机译:创建可控且可预测的微环境以及计算模型的先进细胞培养系统可能是优化细胞感染效率的有用工具。在本文中,我们将对病毒-宿主感染系统进行现象学研究,并开发一种多层微流控平台,用于精确地调节病毒从扩散受限机制到对流占主导地位的机制。数学模型预测了系统本身内部发展的对流-扩散状态,并确定了主要的物质传输现象。携带增强型绿色荧光蛋白(EGFP)转基因的腺病毒载体可在不同的感染复数(MOI)下使用,以在标准静态和灌注条件下感染多种细胞类型。我们的结果验证了数学模型,并证明了即使在MOI较低的情况下,通过微流控平台灌注引起的感染过程如何也会导致腺病毒感染效率的提高。在更长的时间点上,这一点尤其明显,因为稳态条件的建立保证了靠近细胞的恒定病毒浓度,从而增强了感染效率。最后,我们介绍了有效MOI的概念,它是微流体感染的一个更合适的变量,它考虑了特定时间每个细胞溶液中腺病毒的数量。

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