Whitelaw V A, Cowan J D
J Neurosci. 1981 Dec;1(12):1369-87. doi: 10.1523/JNEUROSCI.01-12-01369.1981.
A computational model is presented which simulates the development and regeneration of orderly connections between retinal fibers and tectal cells in frogs and goldfish. The model distinguishes two aspects of retinotectal connectivity: (1) the contact adhesion between retinal fibers and tectal cells as mediated by fixed chemospecific markers and (2) the formation of modifiable synapses between them. Chemospecificity is assumed to be an intrinsic property of both the retina and tectum and is modeled as a graded distribution of a binding determinant or marker. Synapse formation depends upon the timing of neural activity as well as on the intinsic chemospecificity of retinotectal contacts. In addition to the normal development and regeneration of the retinotectal map, the model simulates the compressed, expanded, translocated, and rotated maps that have been found in surgically manipulated contexts. There examples of plasticity in the retinotectal map can be simulated without assuming any changes in the marker distributions. Moreover, the model demonstrates that a very shallow gradient of a single marker suffices to organize retinotectal connections in a variety of contexts.
本文提出了一个计算模型,该模型模拟了青蛙和金鱼视网膜纤维与顶盖细胞之间有序连接的发育和再生过程。该模型区分了视网膜-顶盖连接的两个方面:(1)由固定化学特异性标记介导的视网膜纤维与顶盖细胞之间的接触黏附;(2)它们之间可修饰突触的形成。化学特异性被认为是视网膜和顶盖的固有属性,并被建模为结合决定因素或标记的分级分布。突触的形成取决于神经活动的时间以及视网膜-顶盖接触的固有化学特异性。除了视网膜-顶盖图谱的正常发育和再生外,该模型还模拟了在手术操作情况下发现的压缩、扩展、移位和旋转图谱。视网膜-顶盖图谱中的这些可塑性实例可以在不假设标记分布有任何变化的情况下进行模拟。此外,该模型表明,单个标记的非常浅的梯度足以在各种情况下组织视网膜-顶盖连接。