Buckmaster P S, Wenzel H J, Kunkel D D, Schwartzkroin P A
Department of Neurological Surgery, University of Washington, Seattle 98195, USA.
J Comp Neurol. 1996 Mar 4;366(2):271-92. doi: 10.1002/(sici)1096-9861(19960304)366:2<270::aid-cne7>3.0.co;2-2.
The axon collateralization patterns and synaptic connections of intracellularly labeled and electrophysiologically identified mossy cells were studied in rat hippocampus. Light microscopic analysis of 11 biocytin-filled cells showed that mossy cell axon arbors extended through an average of 57% of the total septotemporal length of the hippocampus (summated two-dimensional length, not adjusted for tissue shrinkage). Axon collaterals were densest in distant lamellae rather than in lamellae near the soma. Most of the axon was concentrated in the inner one-third of the molecular layer, with the hilus containing an average of only 26% of total axon length and the granule cell layer containing an average of only 7%. Ultrastructural analysis was carried out on three additional intracellularly stained mossy cells, in which axon collaterals and synaptic targets were examined in serial sections of chosen axon segments. In the central and subgranular regions of the hilus, mossy cell axons established a low density of synaptic contacts onto dendritic shafts, neuronal somata, and occasional dendritic spines. Most hilar synapses were made relatively close to the mossy cell somata. At greater distances from the labeled mossy cell (1-2 mm along the septotemporal axis), the axon collaterals ramified predominantly within the inner molecular layer and made a high density of asymmetric synaptic contacts almost exclusively onto dendritic spines. Quantitative measurements indicated that more than 90% of mossy cell synaptic contacts in the ipsilateral hippocampus are onto spines of proximal dendrites of presumed granule cells. These results are consistent with a primary mossy cell role in an excitatory associational network with granule cells of the dentate gyrus.
在大鼠海马体中研究了细胞内标记和电生理鉴定的苔藓细胞的轴突侧支模式和突触连接。对11个生物素填充细胞的光学显微镜分析表明,苔藓细胞轴突分支平均延伸穿过海马体总隔颞长度的57%(二维总长度,未针对组织收缩进行调整)。轴突侧支在远处的板层中最密集,而不是在胞体附近的板层中。大部分轴突集中在分子层的内三分之一,海马体包含的轴突总长度平均仅为26%,颗粒细胞层平均仅为7%。对另外三个细胞内染色的苔藓细胞进行了超微结构分析,在选定轴突段的连续切片中检查了轴突侧支和突触靶点。在海马体的中央和颗粒下区域,苔藓细胞轴突在树突干、神经元胞体和偶尔的树突棘上建立了低密度的突触联系。大多数海马体突触相对靠近苔藓细胞胞体形成。在距标记的苔藓细胞更远的距离(沿隔颞轴1-2毫米),轴突侧支主要在分子层内侧分支,并几乎专门在树突棘上形成高密度的不对称突触联系。定量测量表明,同侧海马体中超过90%的苔藓细胞突触联系位于假定颗粒细胞近端树突的棘上。这些结果与苔藓细胞在与齿状回颗粒细胞的兴奋性联合网络中的主要作用一致。