Simat Marija, Parpan Franziska, Fritschy Jean-Marc
Institute of Pharmacology and Toxicology, University of Zurich, CH-8057 Zurich, Switzerland.
J Comp Neurol. 2007 Jan 1;500(1):71-83. doi: 10.1002/cne.21142.
Interneurons of the cerebellum granule cell layer (GCL) form distinct populations. Golgi cells extend dendrites in the molecular layer (ML) and innervate granule cells. In contrast, Lugaro cells have dendrites confined to the GCL but innervate interneurons in the ML, and globular cells have both their dendrites and axons in the ML. The latter cells were described recently and remain poorly characterized. Although several neurochemical markers have been associated selectively with GCL interneurons, it is unclear how they relate to their morphological classification and neurochemical phenotype (glycinergic and/or gamma-aminobutyric acid [GABA]ergic). Here, we performed a detailed characterization of GCL interneurons in mice expressing enhanced green fluorescent protein (GFP) in glycinergic and GABAergic neurons, respectively. By using immunofluorescence for metabotropic glutamate receptor 2 (mGluR2) and neurogranin as markers, we demonstrate the existence of five non-overlapping subsets of Golgi cells: about 65% are glycinergic/GABAergic and co-express both markers. Two small subsets (5-10%) also contain both neurotransmitters but express only mGluR2; they are distinguished by cell body size and location in the GCL. The fourth subset (15%) is GABAergic only and expresses neurogranin. The fifth subset (5%) is glycinergic only and lacks both markers. Thus, the heterogeneity of Golgi cells suggests that they belong to specific functional circuits and are differentially regulated by mGluRs and Ca(2+)-calmodulin-dependent signaling pathways. In contrast to Golgi cells, Lugaro and globular cells are glycinergic/GABAergic and lack mGluR2 and neurogranin. They each represent at least 15% of GCL interneurons and extensively innervate stellate and basket cells, but not Purkinje cells, emphasizing their contribution to inhibitory control of ML interneurons.
小脑颗粒细胞层(GCL)的中间神经元形成不同的群体。高尔基细胞在分子层(ML)中延伸树突并支配颗粒细胞。相比之下,卢加罗细胞的树突局限于GCL,但支配ML中的中间神经元,而球细胞的树突和轴突都在ML中。后一种细胞是最近才被描述的,其特征仍然不明确。尽管几种神经化学标记已被选择性地与GCL中间神经元相关联,但尚不清楚它们如何与其形态学分类和神经化学表型(甘氨酸能和/或γ-氨基丁酸[GABA]能)相关。在这里,我们对分别在甘氨酸能和GABA能神经元中表达增强型绿色荧光蛋白(GFP)的小鼠的GCL中间神经元进行了详细表征。通过使用代谢型谷氨酸受体2(mGluR2)和神经颗粒素的免疫荧光作为标记,我们证明了高尔基细胞存在五个不重叠的亚群:约65%是甘氨酸能/GABA能,并共表达这两种标记。两个小亚群(5 - 10%)也同时含有这两种神经递质,但只表达mGluR2;它们通过细胞体大小和在GCL中的位置来区分。第四个亚群(15%)仅为GABA能,并表达神经颗粒素。第五个亚群(5%)仅为甘氨酸能,且缺乏这两种标记。因此,高尔基细胞的异质性表明它们属于特定的功能回路,并受到mGluRs和钙调蛋白依赖性信号通路的差异调节。与高尔基细胞不同,卢加罗细胞和球细胞是甘氨酸能/GABA能,且缺乏mGluR2和神经颗粒素。它们各自至少占GCL中间神经元的15%,并广泛支配星状细胞和篮状细胞,但不支配浦肯野细胞,这突出了它们对ML中间神经元抑制性控制的贡献。