Nunzi M G, Mugnaini E
Institute of Neuroscience, Northwestern University, Chicago, Illinois 60611, USA.
J Comp Neurol. 2000 Jun 19;422(1):55-65. doi: 10.1002/(sici)1096-9861(20000619)422:1<55::aid-cne4>3.0.co;2-9.
The unipolar brush cells (UBCs), a class of neurons recently identified in the granular layer of the vestibulocerebellum, receive excitatory synaptic input from mossy fibers (MFs) in the form of a giant glutamatergic synapse. UBCs are provided with axons that bear synaptic endings situated at the center of glomeruli, similar to cerebellar MF afferents. A single MF stimulus evokes a prolonged train of action potentials in the UBC (Rossi et al., 1995), which is presumably distributed to postsynaptic targets. Knowledge of the synaptic connections of UBC axons is essential to define the role of these cells in the integration of vestibular signals in the cerebellar circuitry. To evaluate these connections, the nodulus (folium X) was isolated from vermal slices of postnatal day 8 mice, cultured for 2-4 or 15-30 days in vitro, and studied by electron and fluorescence microscopy. The peak of degeneration of extrinsic MF terminals, which have been severed from the parent cell bodies, was observed at 2 days in vitro (DIV). Quantification of degenerating and nondegenerating (e.g., intrinsic) MF terminals indicated that about half of the MF terminals were provided by local UBC axons synapsing on dendrites of granule cells and other UBCs. The proportion of nondegenerating vs. degenerating MF terminals terminating on UBCs also indicated that approximately two-thirds of the intrinsic MFs are involved in UBC-UBC connections. In long-term cultures, the granular layer appeared well preserved and the UBC axons formed an extensive system of MF collaterals. It is suggested that UBCs may act by spatially amplifying vestibular inputs carried by extrinsic MFs.
单极刷细胞(UBCs)是最近在前庭小脑颗粒层中发现的一类神经元,它们通过巨大的谷氨酸能突触形式从苔藓纤维(MFs)接收兴奋性突触输入。UBCs具有轴突,其突触末梢位于小球中心,类似于小脑MF传入纤维。单个MF刺激可在UBC中引发一系列持续的动作电位(Rossi等人,1995年),这些动作电位可能会传递到突触后靶点。了解UBC轴突的突触连接对于确定这些细胞在小脑回路中前庭信号整合中的作用至关重要。为了评估这些连接,从出生后第8天小鼠的蚓部切片中分离出小结(小叶X),在体外培养2 - 4天或15 - 30天,然后通过电子显微镜和荧光显微镜进行研究。从母细胞体切断的外在MF终末的退化高峰期在体外培养2天(DIV)时观察到。对退化和未退化(例如,内在的)MF终末的定量分析表明,大约一半的MF终末由突触连接在颗粒细胞和其他UBC树突上的局部UBC轴突提供。终止于UBCs的未退化与退化MF终末的比例也表明,大约三分之二的内在MF参与了UBC - UBC连接。在长期培养中,颗粒层看起来保存良好,UBC轴突形成了一个广泛的MF侧支系统。有人提出,UBCs可能通过在空间上放大由外在MF携带的前庭输入而起作用。