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3D 细胞聚集体放大扩散信号。

3D cell aggregates amplify diffusion signals.

机构信息

Department of Cancer and Genomic Sciences, College of Medicine and Health, University of Birmingham, Birmingham, United Kingdom.

Drug Metabolism and Pharmacokinetics, Research and Early Development, Cardiovascular, Renal and Metabolism (CVRM), AstraZeneca, Gothenburg, Sweden.

出版信息

PLoS One. 2024 Sep 12;19(9):e0310109. doi: 10.1371/journal.pone.0310109. eCollection 2024.

Abstract

Biophysical models can predict the behavior of cell cultures including 3D cell aggregates (3DCAs), thereby reducing the need for costly and time-consuming experiments. Specifically, mass transfer models enable studying the transport of nutrients, oxygen, signaling molecules, and drugs in 3DCA. These models require the defining of boundary conditions (BC) between the 3DCA and surrounding medium. However, accurately modeling the BC that relates the inner and outer boundary concentrations at the border between the 3DCA and the medium remains a challenge that this paper addresses using both theoretical and experimental methods. The provided biophysical analysis indicates that the concentration of molecules inside boundary is higher than that at the outer boundary, revealing an amplification factor that is confirmed by a particle-based simulator (PBS). Due to the amplification factor, the PBS confirms that when a 3DCA with a low concentration of target molecules is introduced to a culture medium with a higher concentration, the molecule concentration in the medium rapidly decreases. The theoretical model and PBS simulations were used to design a pilot experiment with liver spheroids as the 3DCA and glucose as the target molecule. Experimental results agree with the proposed theory and derived properties.

摘要

生物物理模型可以预测细胞培养物的行为,包括 3D 细胞聚集体(3DCA),从而减少昂贵且耗时的实验的需求。具体来说,质量传递模型能够研究 3DCA 中营养物质、氧气、信号分子和药物的传输。这些模型需要定义 3DCA 和周围介质之间的边界条件(BC)。然而,准确地模拟与 3DCA 和介质之间边界的内部和外部边界浓度相关的 BC 仍然是一个挑战,本文使用理论和实验方法来解决这个问题。提供的生物物理分析表明,边界内分子的浓度高于外部边界的浓度,揭示了一个放大因子,这一点被基于粒子的模拟器(PBS)所证实。由于放大因子,PBS 证实了当一个目标分子浓度较低的 3DCA 被引入到一个分子浓度较高的培养基中时,培养基中的分子浓度会迅速下降。理论模型和 PBS 模拟被用于设计一个带有肝球体作为 3DCA 和葡萄糖作为目标分子的初步实验。实验结果与所提出的理论和推导的特性一致。

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