Sotelo Constantino
Sorbonne Universités, UPMC Université Paris 06, INSERM, CNRS, Institut de la Vision, 17, rue Moreau, 75012 Paris, France; Instituto de Neurociencias de Alicante, UMH-CSIC, Universidad Miguel Hernández de Elche, Alicante, Spain.
Neuroscience. 2021 May 10;462:56-69. doi: 10.1016/j.neuroscience.2020.01.019. Epub 2020 Jan 23.
In the last 50 years, our vision of the cerebellum has vastly evolved starting with Voogd's (1967) description of extracerebellar projections' terminations and how the projection maps transformed the presumptive homogeneity of the cerebellar cortex into a more complex center subdivided into transverse and longitudinal distinct functional zones. The picture became still more complex with Richard Hawkes and colleagues' (Gravel et al., 1987) discovery of the biochemical heterogeneity of Purkinje cells (PCs), by screening their molecular identities with monoclonal antibodies. Antigens were expressed in a parasagittal pattern with subsets of PCs either possessing or lacking the respective antigens, which divided the cerebellar cortex into precise longitudinal compartments that are congruent with the projection maps. The correlation of these two maps in adult cerebellum shows a perfect matching of developmental mechanisms. This review discusses a series of arguments in favor of the essential role played by PCs in organizing the microzonation of the cerebellum during development (the "matching" hypothesis).
在过去的50年里,我们对小脑的认识有了巨大的发展,始于沃格德(1967年)对小脑外投射终止的描述,以及投射图谱如何将小脑皮质假定的同质性转变为一个更复杂的中心,该中心细分为横向和纵向不同的功能区。随着理查德·霍克斯及其同事(格拉韦尔等人,1987年)通过用单克隆抗体筛选浦肯野细胞(PCs)的分子身份,发现了浦肯野细胞的生化异质性,情况变得更加复杂。抗原以矢状旁模式表达,部分浦肯野细胞拥有或缺乏相应抗原,这将小脑皮质划分为与投射图谱一致的精确纵向区室。这两张图谱在成年小脑中的相关性显示出发育机制的完美匹配。本综述讨论了一系列论据,支持浦肯野细胞在发育过程中组织小脑微区划方面所起的重要作用(“匹配”假说)。