Sillitoe Roy V, Chung Seung-Hyuk, Fritschy Jean-Marc, Hoy Monica, Hawkes Richard
Department of Cell Biology and Anatomy, Genes and Development Research Group, and Hotchkiss Brain Institute, Faculty of Medicine, The University of Calgary, Calgary, Alberta, Canada.
J Neurosci. 2008 Mar 12;28(11):2820-6. doi: 10.1523/JNEUROSCI.4145-07.2008.
Despite the general uniformity in cellular composition of the adult cerebellar cortex, there is a complex underlying pattern of parasagittal stripes of Purkinje cells with characteristic molecular phenotypes and patterns of connectivity. It is not known whether interneuron processes are restricted at stripe boundaries. To begin to address the issue, three strategies were used to explore how cerebellar Golgi cell dendrites are organized with respect to parasagittal stripes: first, double immunofluorescence staining combining anti-neurogranin to identify Golgi cell dendrites with the Purkinje cell compartmentation antigens zebrin II/aldolase C, HNK-1, and phospholipase Cbeta4; second, zebrin II immunohistochemistry combined with a rapid Golgi-Cox impregnation procedure to reveal Golgi cell dendritic arbors; third, stripe antigen expression was used on sections of a GlyT2-EGFP transgenic mouse in which reporter expression is prominent in Golgi cell dendrites. In each case, the dendritic projections of Golgi cells were studied in the vicinity of Purkinje cell stripe boundaries. The data presented here show that the dendrites of a cerebellar interneuron, the Golgi cell, respect the fundamental cerebellar stripe cytoarchitecture.
尽管成年小脑皮质的细胞组成总体上具有一致性,但浦肯野细胞的矢状旁条纹存在复杂的潜在模式,具有特征性的分子表型和连接模式。目前尚不清楚中间神经元的突起是否在条纹边界处受到限制。为了开始解决这个问题,我们采用了三种策略来探索小脑高尔基细胞的树突相对于矢状旁条纹是如何组织的:第一,双重免疫荧光染色,将抗神经颗粒素与浦肯野细胞分区抗原zebrin II/醛缩酶C、HNK-1和磷脂酶Cβ4结合以识别高尔基细胞的树突;第二,zebrin II免疫组织化学结合快速高尔基-考克斯浸染程序以揭示高尔基细胞的树突分支;第三,在GlyT2-EGFP转基因小鼠的切片上使用条纹抗原表达,其中报告基因在高尔基细胞的树突中显著表达。在每种情况下,都在浦肯野细胞条纹边界附近研究了高尔基细胞的树突投射。此处呈现的数据表明,小脑中间神经元高尔基细胞的树突遵循基本的小脑条纹细胞结构。