Streffing-Hellhake P, Luft A R, Hosp J A
Clinic of Neurology and Neurophysiology, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Germany.
Division of Vascular Neurology and Neurorehabilitation, Department of Neurology, University Hospital of Zurich, Zurich, Switzerland; cereneo, Center for Neurology and Rehabilitation, Vitznau, Switzerland.
Neuroscience. 2020 Aug 21;442:17-28. doi: 10.1016/j.neuroscience.2020.06.039. Epub 2020 Jul 4.
Motor learning depends on plastic reorganization of neural networks within the primary motor cortex (M1). In the circuitry of M1, integration and processing of afferent inputs is executed by pyramidal neurons of layer II/III. Thus, an involvement of these layer II/III pyramids in learning-induced changes is highly plausible. We therefore analyzed dendritic plasticity in layer II/III pyramidal cells on Golgi-Cox silver-impregnated sections after training of a forelimb reaching task. Based on their location within layer II/III, neurons were assigned to either a superficial or a deep population. After training, morphological changes occurred in both superficial and deep layer II/III pyramids. Overall, a decrease in dendritic length could be observed. In detail, superficial cells showed a significant reduction in the length of the apical dendrite after training ended in contrast to deep layer II/III pyramids, where dendritic length initially remained stable. Both types of neurons showed a transient increment in complexity of the distal apical dendrite 30 days after training. Findings were different in basal dendrites: length and complexity continuously decreased in superficial and deep layer II/III pyramids. Spine density increased in apical and basal dendrites of both superficial and deep layer II/III neurons, likely an effect of ageing that occurred independently from motor learning. This increase in spine density was accompanied with a morphological change towards stubby- and mushroom-like spines. Thus, profound but delayed changes occurred within the dendritic compartment of layer II/III pyramidal cells.
运动学习依赖于初级运动皮层(M1)内神经网络的可塑性重组。在M1的神经回路中,传入输入的整合和处理由第II/III层的锥体神经元执行。因此,这些第II/III层锥体神经元参与学习诱导的变化是非常合理的。因此,我们在训练前肢够物任务后,分析了高尔基-考克斯银浸染切片上第II/III层锥体细胞的树突可塑性。根据它们在第II/III层内的位置,神经元被分为浅层或深层群体。训练后,浅层和深层第II/III层锥体均发生形态变化。总体而言,可以观察到树突长度减少。具体而言,与深层第II/III层锥体相反,浅层细胞在训练结束后顶树突长度显著减少,而深层第II/III层锥体的树突长度最初保持稳定。两种类型的神经元在训练后30天,远端顶树突的复杂性均出现短暂增加。基树突的结果不同:浅层和深层第II/III层锥体的基树突长度和复杂性持续下降。浅层和深层第II/III层神经元的顶树突和基树突棘密度均增加,这可能是与运动学习无关的衰老效应。这种棘密度的增加伴随着向短粗状和蘑菇状棘的形态变化。因此,第II/III层锥体细胞的树突区发生了深刻但延迟的变化。