首页> 外文期刊>Journal of the Royal Society Interface >Multi-scale modelling of the dynamics of cell colonies: insights into cell-adhesion forces and cancer invasion from in silico simulations
【24h】

Multi-scale modelling of the dynamics of cell colonies: insights into cell-adhesion forces and cancer invasion from in silico simulations

机译:细胞殖民动力学的多规模建模:硅模拟中细胞 - 粘附力和癌症侵袭的见解

获取原文
获取原文并翻译 | 示例
           

摘要

Studying the biophysical interactions between cells is crucial to understanding how normal tissue develops, how it is structured and also when malfunctions occur. Traditional experiments try to infer events at the tissue level after observing the behaviour of and interactions between individual cells. This approach assumes that cells behave in the same biophysical manner in isolated experiments as they do within colonies and tissues. In this paper, we develop a multi-scale multi-compartment mathematical model that accounts for the principal biophysical interactions and adhesion pathways not only at a cell-cell level but also at the level of cell colonies (in contrast to the traditional approach). Our results suggest that adhesion/separation forces between cells may be lower in cell colonies than traditional isolated single-cell experiments infer. As a consequence, isolated single-cell experiments may be insufficient to deduce important biological processes such as single-cell invasion after detachment from a solid tumour. The simulations further show that kinetic rates and cell biophysical characteristics such as pressure-related cell-cycle arrest have a major influence on cell colony patterns and can allow for the development of protrusive cellular structures as seen in invasive cancer cell lines independent of expression levels of pro-invasion molecules.
机译:研究细胞间的生物物理相互作用对于理解正常组织如何发育、结构如何以及故障何时发生至关重要。传统实验试图在观察单个细胞的行为和相互作用后,在组织水平上推断事件。这种方法假设细胞在孤立实验中的行为与在菌落和组织中的行为相同。在本文中,我们开发了一个多尺度多室数学模型,该模型不仅在细胞水平上,而且在细胞集落水平上(与传统方法相比)解释了主要的生物物理相互作用和粘附途径。我们的结果表明,细胞集落中细胞间的粘附力/分离力可能比传统的单细胞实验推断的要低。因此,孤立的单细胞实验可能不足以推断出重要的生物学过程,例如从实体肿瘤分离后的单细胞侵袭。模拟进一步表明,动力学速率和细胞生物物理特性(如压力相关的细胞周期阻滞)对细胞集落模式有重大影响,并可使侵袭性癌细胞系中出现的突入性细胞结构的发育独立于促侵袭分子的表达水平。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号