Meinhardt H
Differentiation. 1983;24(3):191-202. doi: 10.1111/j.1432-0436.1983.tb01319.x.
We propose that the prestalk/prespore pattern in Dictyostelium is generated in two steps: In a first process, an intermingled, non-position dependent prestalk/prespore pattern is generated by a cell-restricted autocatalysis and the antagonistic action of a long-ranging substrate which becomes depleted during this autocatalysis. By computer simulations we show that the assumed interaction accounts for several experimentally observed features of the prestalk/prespore pattern: The size-independent ratio of both cell types, the pattern regulation after removal of one cell type, the development towards one or the other pathway before the slug obtains its final shape or even before aggregation is completed. Our hypothetical substrate may be identical with an experimentally found differentiation-inducing factor (DIF). Alternative molecular realizations of the basic mechanism are discussed. A second process leads to the aggregation of the prestalk cells in a particular region of the aggregate, the future tip region. Interactions which enable tip formation and the coupling between the prestalk/prespore and the tip-forming system are discussed. Our model shows that the formation of a single large patch of differentiated cells and its size regulation requires conflicting parameters. By a separation into a mechanism which determines the position and a second one which determines the size of a structure, each mechanism can be optimized individually without requiring compromises for the other. Such a separation also seems to occur in other developmental systems.
我们提出,盘基网柄菌中的前柄细胞/前孢子细胞模式是分两步形成的:在第一步过程中,一种由细胞限制的自催化作用以及一种在自催化过程中会耗尽的远距离底物的拮抗作用,产生了一种混合的、不依赖位置的前柄细胞/前孢子细胞模式。通过计算机模拟,我们表明所假设的相互作用解释了前柄细胞/前孢子细胞模式的几个实验观察特征:两种细胞类型与大小无关的比例、去除一种细胞类型后的模式调节、在蛞蝓获得最终形状之前甚至在聚集完成之前向一种或另一种途径的发育。我们假设的底物可能与实验发现的分化诱导因子(DIF)相同。还讨论了基本机制的其他分子实现方式。第二步过程导致前柄细胞在聚集体的特定区域,即未来的顶端区域聚集。讨论了促成顶端形成的相互作用以及前柄细胞/前孢子细胞与顶端形成系统之间的耦合。我们的模型表明,形成单个大的分化细胞斑块及其大小调节需要相互冲突的参数。通过将其分离为决定位置的机制和决定结构大小的第二个机制,每个机制都可以单独优化,而无需为另一个机制做出妥协。这种分离似乎也发生在其他发育系统中。