Zampighi G, Kreman M, Ramón F, Moreno A L, Simon S A
Department of Anatomy, Jerry Lewis Neuromuscular Research Center, UCLA School of Medicine 90024.
J Cell Biol. 1988 May;106(5):1667-78. doi: 10.1083/jcb.106.5.1667.
Gap junctions between crayfish lateral axons were studied by combining anatomical and electrophysiological measurements to determine structural changes associated during uncoupling by axoplasmic acidification. In basal conditions, the junctional resistance, Rj, was approximately 60-80 k omega and the synapses appeared as two adhering membranes; 18-20-nm overall thickness, containing transverse densities (channels) spanning both membranes and the narrow extracellular gap (4-6 nm). In freeze-fracture replicas, the synapses contained greater than 3 X 10(3) gap junction plaques having a total of approximately 3.5 X 10(5) intramembrane particles. "Single" gap junction particles represented approximately 10% of the total number of gap junction particles present in the synapse. Therefore, in basal conditions, most of the gap junction particles were organized in plaques. Moreover, correlations of the total number of gap junction particles with Rj suggested that most of the junctional particles in plaques corresponded to conducting channels. Upon acidification of the axoplasm to pH 6.7-6.8, the junctional resistance increased to approximately 300 k omega and action potentials failed to propagate across the septum. Morphological measurements showed that the total number of gap junction particles in plaques decreased approximately 11-fold to 3.1 X 10(4) whereas the number of single particles dispersed in the axolemmae increased significantly. Thin sections of these synapses showed that the width of the extracellular gap increased from 4-6 nm in basal conditions to 10-20 nm under conditions where axoplasmic pH was 6.7-6.8. These observations suggest that single gap junction particles dispersed in the synapse most likely represent hemi-channels produced by the dissasembly of channels previously arranged in plaques.
通过结合解剖学和电生理学测量方法,研究小龙虾侧轴突之间的缝隙连接,以确定轴浆酸化解偶联过程中相关的结构变化。在基础条件下,连接电阻Rj约为60 - 80 kΩ,突触表现为两个紧密相连的膜;总厚度为18 - 20nm,包含横跨两层膜和狭窄细胞外间隙(4 - 6nm)的横向致密结构(通道)。在冷冻蚀刻复制品中,突触含有超过3×10³个缝隙连接斑块,总共约有3.5×10⁵个膜内颗粒。“单个”缝隙连接颗粒约占突触中缝隙连接颗粒总数的10%。因此,在基础条件下,大多数缝隙连接颗粒排列成斑块。此外,缝隙连接颗粒总数与Rj的相关性表明,斑块中的大多数连接颗粒对应于传导通道。当轴浆酸化至pH 6.7 -