Ichimura T, Hashimoto P H
Department of Anatomy, Osaka University Medical School, Japan.
J Neurocytol. 1988 Feb;17(1):3-12. doi: 10.1007/BF01735373.
Structural components in the synaptic cleft were examined in cerebellar excitatory synapses by conventional electron microscopy and by rapid freezing followed by freeze-substitution or deep etching. Two transverse components and one parallel element were identified in the clefts of rapidly frozen and freeze-substituted synapses: (i) bridging fibrils, 4-6 nm in diameter, that span the cleft; (ii) columnar pegs, 4-6 nm wide and 8-15 nm high, projecting from the postsynaptic surface; and (iii) intervening fine fibrils running parallel to the apposed synaptic membranes. These were more clearly visible in deep-etched synapses, although the postsynaptic pegs were difficult to distinguish from intramembrane particles in the cross-fractured postsynaptic membranes. Deep etching also revealed other fibrils on the cytoplasmic surface of the postsynaptic membrane. These appear to contact the membrane surface or the intramembrane particles. Freeze-substituted materials also displayed the fibrillar components in the postsynaptic dense fuzz, but failed to display the presynaptic dense projections typically observed in thin sections or deep-etched replicas of the conventionally fixed materials. The bridging fibrils are likely to play a mechanical role in holding the synapse together, while the short pegs may be integral parts of the receptor molecules.
通过传统电子显微镜以及快速冷冻后进行冷冻置换或深度蚀刻的方法,对小脑兴奋性突触中突触间隙的结构成分进行了研究。在快速冷冻并经冷冻置换处理的突触间隙中,鉴定出了两种横向成分和一种平行成分:(i)桥连纤维,直径为4 - 6纳米,横跨突触间隙;(ii)柱状短桩,宽4 - 6纳米,高8 - 15纳米,从突触后表面突出;(iii)与相对的突触膜平行排列的中间细纤维。这些在深度蚀刻的突触中更清晰可见,尽管在突触后膜的交叉断裂处,突触后短桩难以与膜内颗粒区分开来。深度蚀刻还揭示了突触后膜细胞质表面的其他纤维。这些纤维似乎与膜表面或膜内颗粒接触。冷冻置换材料也显示出突触后致密绒毛中的纤维成分,但未能显示出在传统固定材料的薄切片或深度蚀刻复制品中通常观察到的突触前致密突起。桥连纤维可能在将突触维系在一起方面发挥机械作用,而短桩可能是受体分子的组成部分。