Gouzé J L, Lasry J M, Changeux J P
Biol Cybern. 1983;46(3):207-15. doi: 10.1007/BF00336802.
The biochemical model presented concerns a critical step of the development of skeletal muscle innervation. After invasion of the muscle by exploratory motor axons, several nerve terminals converge from different motoneurons onto each muscle fibre at a single endplate. During the following weeks the redundant innervation disappears: a single nerve ending per muscle fibre becomes stabilized. The model is based on the assumption that the numbers of motoneurons and of muscle fibres remain constant during this evolution and that the selective stabilization of the adult connectivity results from the competition of the active nerve terminals for a postsynaptic retrograde factor mu. At the peak of the multiple innervation, the synthesis of mu by the muscle fiber stops, possibly as a consequence of muscle electrical and/or mechanical activity. The stock of mu becomes limited; a retrograde trans-synaptic diffusion of mu from the muscle to the nerve endings takes place. Within each nerve ending, mu enters into a chemical autocatalytic reaction which results in the production of a presynaptic stabilization factor s. The nerve impulses reaching the nerve terminal initiate this reaction. Any given nerve terminal become stabilized when the concentration of s reaches a threshold value. The mathematical analysis of the model shows that there exists a unique solution which is physically acceptable. Its application and computer simulation predict that only one nerve terminal becomes stabilized per muscle fibre. The model accounts for the experimental observations that the reduction in size of the motor units is not necessarily accompanied by a reduction in the variability of their size. The model also accounts for the acceleration or delay in regression which follows modifications of the chronic activity of the nerve endings and for the variability of the pattern of innervation observed in isogenic organisms. Plausible biochemical hypotheses concerning the factors engaged in the "selective stabilization" of the nerve-endings are discussed.
所提出的生化模型涉及骨骼肌神经支配发育的一个关键步骤。在探索性运动轴突侵入肌肉后,几个神经末梢从不同的运动神经元汇聚到每个肌纤维的单个终板上。在接下来的几周里,多余的神经支配消失:每个肌纤维的单个神经末梢趋于稳定。该模型基于这样的假设,即在这一进化过程中运动神经元和肌纤维的数量保持不变,并且成年连接的选择性稳定是由活跃神经末梢对突触后逆行因子μ的竞争导致的。在多重神经支配的高峰期,肌纤维合成μ可能由于肌肉电活动和/或机械活动而停止。μ的储备变得有限;μ从肌肉向神经末梢发生逆行跨突触扩散。在每个神经末梢内,μ进入一个化学自催化反应,该反应导致产生突触前稳定因子s。到达神经末梢的神经冲动引发此反应。当s的浓度达到阈值时,任何给定的神经末梢就会稳定下来。对该模型的数学分析表明存在一个唯一的、符合实际情况的解。其应用和计算机模拟预测每个肌纤维只有一个神经末梢会稳定下来。该模型解释了实验观察结果,即运动单位大小的减小不一定伴随着其大小变异性的减小。该模型还解释了神经末梢慢性活动改变后回归的加速或延迟以及在同基因生物体中观察到的神经支配模式的变异性。文中还讨论了关于参与神经末梢“选择性稳定”的因素的合理生化假设。