Department of Physiology, University of Pavia, Pavia, Italy.
J Physiol. 2010 Oct 1;588(Pt 19):3639-55. doi: 10.1113/jphysiol.2010.189605.
When Camillo Golgi invented the black reaction in 1873 and first described the fine anatomical structure of the nervous system, he described a ‘big nerve cell’ that later took his name, the Golgi cell of cerebellum (‘Golgi’schen Zellen’, Gustaf Retzius, 1892). The Golgi cell was then proposed as the prototype of type-II interneurons, which form complex connections and exert their actions exclusively within the local network. Santiago Ramón y Cajal (who received the Nobel Prize with Golgi in 1906) proceeded to a detailed description of Golgi cell morphological characteristics, but functional insight remained very limited for many years. The first rediscovery happened in the 1960s, when neurophysiological analysis in vivo revealed that Golgi cells are inhibitory interneurons. This finding promoted the development of two major cerebellar theories, the ‘beam theory’ of John Eccles and the ‘motor learning theory’ of David Marr, in which the Golgi cells regulate the spatial organisation and the gain of input signals to be processed and learned by the cerebellar circuit. However, the matter was not set and a series of pioneering observations using single unit recordings and electronmicroscopy raised new issues that could not be fully explored until the 1990s. Then, the advent of new electrophysiological and imaging techniques in vitro and in vivo demonstrated the cellular and network activities of these neurons. Now we know that Golgi cells, through complex systems of chemical and electrical synapses, effectively control the spatio-temporal organisation of cerebellar responses. The Golgi cells regulate the timing and number of spikes emitted by granule cells and coordinate their coherent activity. Moreover, the Golgi cells regulate the induction of long-term synaptic plasticity along the mossy fibre pathway. Eventually, the Golgi cells transform the granular layer of cerebellum into an adaptable spatio-temporal filter capable of performing several kinds of logical operation. After more than a century, Golgi’s intuition that the Golgi cell had to generate under a new perspective complex ensemble effects at the network level has finally been demonstrated.
当 Camillo Golgi 于 1873 年发明黑反应并首次描述神经系统的精细解剖结构时,他描述了一种后来以他的名字命名的“大神经细胞”,即小脑的 Golgi 细胞(“Golgi’schen Zellen”,Gustaf Retzius,1892)。随后,Golgi 细胞被提议为 II 型中间神经元的原型,这些神经元形成复杂的连接,并仅在局部网络中发挥作用。Santiago Ramón y Cajal(他与 Golgi 一起于 1906 年获得诺贝尔奖)对 Golgi 细胞形态特征进行了详细描述,但多年来,功能见解仍然非常有限。第一个重新发现发生在 20 世纪 60 年代,当时体内神经生理学分析表明,Golgi 细胞是抑制性中间神经元。这一发现促进了两大小脑理论的发展,即 John Eccles 的“梁理论”和 David Marr 的“运动学习理论”,其中 Golgi 细胞调节输入信号的空间组织和增益,以便小脑回路进行处理和学习。然而,事情并没有解决,一系列使用单细胞记录和电子显微镜的开创性观察提出了一些新问题,直到 20 世纪 90 年代才能得到充分探讨。然后,体外和体内新的电生理和成像技术的出现证明了这些神经元的细胞和网络活动。现在我们知道,Golgi 细胞通过化学和电突触的复杂系统,有效地控制小脑反应的时空组织。Golgi 细胞调节颗粒细胞发射尖峰的时间和数量,并协调它们的相干活动。此外,Golgi 细胞调节苔藓纤维途径中长时程突触可塑性的诱导。最终,Golgi 细胞将小脑的颗粒层转化为能够执行多种逻辑运算的自适应时空滤波器。一个多世纪后,Golgi 的直觉——Golgi 细胞必须在网络层面产生新的视角下的复杂集合效应——终于得到了证明。