Geurts F J, Timmermans J, Shigemoto R, De Schutter E
Laboratory of Cell Biology and Histology, University of Antwerp, Groenenborgerlaan 171, B-2020, Antwerp, Belgium.
Neuroscience. 2001;104(2):499-512. doi: 10.1016/s0306-4522(01)00058-6.
The granular layer of the cerebellar cortex consists of densely packed neuronal cells, classified into granule cells and large interneurons. In this study, we provide a comparative survey of large granular layer interneurons in the adult rat cerebellum based on both morphological and neurochemical criteria. To this end, double immunofluorescence histochemistry was performed by combining antibodies against the cytoplasmic antigen Rat-303, calretinin, the metabotropic glutamate receptor mGluR2 and somatostatin. Based on Rat-303/calretinin double immunohistochemistry, three distinct populations of large granular layer interneurons could be discerned: cells immunopositive for Rat-303, calretinin or both. Rat-303 or calretinin single-labeled cells represented Golgi cells and unipolar brush cells, respectively. Rat-303/calretinin double-labeled cells located just underneath the Purkinje cell layer represented Lugaro cells. Morphometrical analysis distinguished two populations of Rat-303-positive Golgi cells according to their location: vermis versus hemisphere. Immunostaining for the metabotropic glutamate receptor mGluR2 combined with Rat-303 or calretinin revealed that the majority of Golgi cells (about 90%) appeared to be mGluR2 positive. Lugaro cells were mGluR2 negative. In addition, a limited population of large polymorphous interneurons in the depth of the granular layer with morphological features resembling Golgi cells also displayed Rat-303/calretinin immunoreactivity and were mGluR2 negative. Double immunohistochemistry for Rat-303 and somatostatin revealed three populations of labeled cells in the depth of the granular layer. Besides double-labeled Golgi cells, Rat-303 or somatostatin single-labeled cells were present. Based on mGluR2/somatostatin and calretinin/somatostatin double immunostainings, Rat-303 single-labeled cells were found to correspond to Rat-303/calretinin-positive, mGluR2-negative Golgi-like cells, while the identity of somatostatin single-labeled cells remained unclear. The data presented in this article elaborate previous reports on the morphological and neurochemical differentiation of large interneurons in the rat cerebellar granular layer. In addition, they indicate that the current classification of these cells into Golgi cells, Lugaro cells and unipolar brush cells does not describe the observed neurochemical heterogeneity.
小脑皮质颗粒层由紧密排列的神经元细胞组成,可分为颗粒细胞和大型中间神经元。在本研究中,我们基于形态学和神经化学标准,对成年大鼠小脑的大型颗粒层中间神经元进行了比较研究。为此,通过将针对细胞质抗原Rat-303、钙视网膜蛋白、代谢型谷氨酸受体mGluR2和生长抑素的抗体相结合,进行了双重免疫荧光组织化学实验。基于Rat-303/钙视网膜蛋白双重免疫组织化学,可识别出大型颗粒层中间神经元的三个不同群体:对Rat-303、钙视网膜蛋白或两者呈免疫阳性的细胞。Rat-303或钙视网膜蛋白单标记细胞分别代表高尔基细胞和单极刷细胞。位于浦肯野细胞层正下方的Rat-303/钙视网膜蛋白双标记细胞代表卢加罗细胞。形态计量分析根据其位置区分出两种Rat-303阳性高尔基细胞群体:蚓部与半球。将代谢型谷氨酸受体mGluR2与Rat-303或钙视网膜蛋白结合进行免疫染色显示,大多数高尔基细胞(约90%)似乎为mGluR2阳性。卢加罗细胞为mGluR2阴性。此外,颗粒层深处一群形态特征类似于高尔基细胞的大型多形中间神经元也显示出Rat-303/钙视网膜蛋白免疫反应性,且为mGluR2阴性。Rat-303和生长抑素的双重免疫组织化学显示颗粒层深处有三个标记细胞群体。除了双标记的高尔基细胞外,还存在Rat-303或生长抑素单标记细胞。基于mGluR2/生长抑素和钙视网膜蛋白/生长抑素双重免疫染色,发现Rat-303单标记细胞对应于Rat-303/钙视网膜蛋白阳性、mGluR2阴性的高尔基样细胞,而生长抑素单标记细胞的身份仍不清楚。本文所呈现的数据详细阐述了先前关于大鼠小脑颗粒层大型中间神经元形态学和神经化学分化的报道。此外,这些数据表明,目前将这些细胞分为高尔基细胞、卢加罗细胞和单极刷细胞的分类方法并不能描述所观察到的神经化学异质性。