Tranquillo R T, Alt W
Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis 55455, USA.
J Math Biol. 1996;34(4):361-412. doi: 10.1007/BF00167941.
The proposed mathematical model investigates the simplified cytomechanics of cell shape change driven by stochastic stimulation from chemosensory receptors. The cytomechanical component of our model describes the dynamical distribution of F-actin and associated forces in an idealized cortical actin network around the cell periphery. The chemosensory component describes the distribution of chemotactic receptors in the cell membrane surrounding the cortex, where bound receptors give rise to an intracellular signal which modulates some property of the cortical network. As in our earlier models, an account is made for (1) the reactive, contractive properties of cortical actin, but here also for a stress induced by curvature of the cortex-membrane complex which carries an effective surface tension, and (2) statistical fluctuations in receptor binding, but generalized here to include statistical fluctuations in the spatial distribution of receptors, entirely determined by the additional prescription of membrane diffusion coefficients along with total receptor number, receptor binding rate constants and the local concentration field of chemotactic factor. We simplify the analysis by restricting the model to a prototype in which viscous stresses in the cortical network are negligible and the radial extension of the cell cortex is a prescribed function of the cortical actin concentration. We assume in particular that the assembly rate of cortical actin depends on the local density of bound receptors. These assumptions lead to a 4th-order parabolic differential equation on the unit circle coupled to a system of stochastic differential equations. We characterize via bifurcation analysis, stochastic simulations, and analytical correlation functions the spatial-temporal pattern of cell morphology under the influence of fluctuations in the bound receptor distribution for the case of a uniform concentration field of chemotactic factor. In addition to addressing the biological significance of our model, we remark on its relevance to the generic problem of the influence of correlated stochastic perturbations on spatial patterns in morphogenetic media.
所提出的数学模型研究了由化学感应受体的随机刺激驱动的细胞形状变化的简化细胞力学。我们模型的细胞力学部分描述了围绕细胞周边的理想化皮质肌动蛋白网络中F-肌动蛋白和相关力的动态分布。化学感应部分描述了皮质周围细胞膜中趋化受体的分布,其中结合的受体产生细胞内信号,该信号调节皮质网络的某些特性。与我们早期的模型一样,考虑了(1)皮质肌动蛋白的反应性、收缩性,但这里还考虑了携带有效表面张力的皮质-膜复合体曲率所诱导的应力,以及(2)受体结合的统计波动,但这里进行了推广,以包括受体空间分布的统计波动,这完全由膜扩散系数的额外规定以及总受体数量、受体结合速率常数和趋化因子的局部浓度场决定。我们通过将模型限制为一种原型来简化分析,在该原型中皮质网络中的粘性应力可忽略不计,并且细胞皮质的径向延伸是皮质肌动蛋白浓度的规定函数。我们特别假设皮质肌动蛋白的组装速率取决于结合受体的局部密度。这些假设导致单位圆上的一个四阶抛物型微分方程与一个随机微分方程组耦合。对于趋化因子均匀浓度场的情况,我们通过分岔分析、随机模拟和解析相关函数来表征结合受体分布波动影响下细胞形态的时空模式。除了阐述我们模型的生物学意义外,我们还评论了它与形态发生介质中相关随机扰动对空间模式影响的一般问题的相关性。