Gravel C, Eisenman L M, Sasseville R, Hawkes R
Department of Biochemistry and Laboratory of Neurobiology, Faculty of Medicine, Laval University, Ste-Foy, Quebec, Canada.
J Comp Neurol. 1987 Nov 8;265(2):294-310. doi: 10.1002/cne.902650211.
The Purkinje cells of the cerebellar cortex and the cortical afferent and efferent projections are organized into parallel parasagittal zones. The parasagittal organization is clearly revealed by immunocytochemistry with a monoclonal antibody, mabQ113. The mabQ113 antigen is confined to a subset of Purkinje cells that are clustered together to form an elaborate, highly reproducible pattern of bands and patches, interspersed with similar mabQ113- regions. The mabQ113+ territories have been classified into seven parasagittal bands (P1+-P7+) in each hemicerebellum. The degree of correspondence between the compartments revealed by the anterograde labeling of the olivocerebellar projection and by mabQ113 immunocytochemistry has been explored in the adult rat. Horseradish peroxide-wheat germ agglutinin conjugate was injected as an anterograde tracer into the inferior olivary complex. When the injection site did not encompass all the olive, an incomplete, patchy labeling of the molecular layer was seen in the cerebellar cortex. Labeled zones of the molecular layer were interrupted by unlabeled regions to give a pattern of parasagittal cortical bands. The positions of these bands were compared with the distribution of the mabQ113+ antigenic bands as seen on the two adjacent sections. Labeled climbing fibers were found to terminate on both mabQ113+ and mabQ113- Purkinje cell zones. The mabQ113+/mabQ113- boundaries and the bands of climbing fibers seen by using the anterograde tracer typically coincide. The one consistent exception is the midline band of mabQ113+ Purkinje cells, P1+. The normal olivocerebellar projection is exclusively contralateral and the climbing fiber projection to the paramedian vermis splits P1+ down the middle, implying that it consists of two adjacent mabQ113+ bands not separated by mabQ113-territory. It is likely that the climbing fiber projection to the cerebellar cortex and the distribution of the two Purkinje cell phenotypes share a common compartmental organization.
小脑皮质的浦肯野细胞以及皮质传入和传出投射被组织成平行的矢状旁区。用单克隆抗体mabQ113进行免疫细胞化学可清楚地显示矢状旁组织。mabQ113抗原局限于浦肯野细胞的一个亚群,这些细胞聚集在一起形成一种精细的、高度可重复的条带和斑块模式,其间散布着类似的mabQ113阴性区域。在每个小脑半球中,mabQ113阳性区域已被分为七个矢状旁带(P1 + -P7 +)。在成年大鼠中,研究了橄榄小脑投射的顺行标记和mabQ113免疫细胞化学所揭示的区室之间的对应程度。将辣根过氧化物酶-小麦胚凝集素结合物作为顺行示踪剂注入下橄榄复合体。当注射部位未涵盖整个橄榄时,在小脑皮质的分子层中可见不完全的、斑块状的标记。分子层的标记区被未标记区域中断,形成矢状旁皮质带的模式。将这些带的位置与在相邻的两个切片上看到的mabQ113阳性抗原带的分布进行比较。发现标记的攀缘纤维终止于mabQ113阳性和mabQ113阴性浦肯野细胞区。使用顺行示踪剂看到的mabQ113阳性/mabQ113阴性边界和攀缘纤维带通常是一致的。唯一一致的例外是mabQ113阳性浦肯野细胞的中线带,即P1 +。正常的橄榄小脑投射完全是对侧的,并且向旁正中蚓部的攀缘纤维投射将P1 +从中间分开,这意味着它由两个相邻的mabQ113阳性带组成,中间没有被mabQ113阴性区域隔开。很可能向小脑皮质的攀缘纤维投射和两种浦肯野细胞表型的分布共享一个共同的区室组织。