Nguyen Hien, Song Mingzhou
Department of Computer Science, New Mexico State University, Las Cruces, NM 88003, USA.
Int J Comput Biol Drug Des. 2011;4(4):361-72. doi: 10.1504/IJCBDD.2011.044444. Epub 2011 Dec 24.
Cellular behaviour depends on and also modifies protein concentration and activity. An integrated cellular and gene interaction model is proposed to reveal this relationship. In this model, protein activity varies spatiotemporally with cellular location, gene interaction, and diffusion. In the meanwhile, cellular behaviour can vary spatially, driven by cell-cell signalling and inhomogeneous protein distribution across cells. This model integrates two components. The first component adopts a variation of the reaction-diffusion mechanism at the gene expression level. The second component is a lattice cellular model based on the Differential Adhesion Hypothesis (DAH) for cell sorting at the cellular level. Cell sorting and tumour invasion were simulated to illustrate the model. This model approximates cellular pattern formation more closely than existing models based on cell density.
细胞行为取决于蛋白质浓度和活性,同时也会对其进行调节。本文提出了一个整合的细胞与基因相互作用模型来揭示这种关系。在该模型中,蛋白质活性随细胞位置、基因相互作用和扩散在时空上发生变化。与此同时,细胞行为会在细胞间信号传导以及细胞间蛋白质分布不均一性的驱动下发生空间变化。该模型整合了两个部分。第一部分在基因表达水平采用了反应扩散机制的变体。第二部分是基于细胞分选的微分粘附假说(DAH)在细胞水平构建的晶格细胞模型。通过模拟细胞分选和肿瘤侵袭来阐释该模型。与现有的基于细胞密度的模型相比,该模型能更精确地模拟细胞模式形成。