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钙在突触前神经末梢中的定位。超微结构和电子微探针分析。

Localization of calcium in presynaptic nerve terminals. An ultrastructural and electron microprobe analysis.

作者信息

McGraw C F, Somlyo A V, Blaustein M P

出版信息

J Cell Biol. 1980 May;85(2):228-41. doi: 10.1083/jcb.85.2.228.

Abstract

Ultrastructural techniques and electron probe microanalysis were used to determine whether or not the smooth endoplasmic reticulum (SER) within presynaptic nerve terminals is a Ca-sequestering site. The three-dimensional structure of the SER was determined from serial sections of synaptosomes. The SER consists of flattened cisterns that may branch and are frequently juxtaposed to mitochondria. To investigate intraterminal Ca sequestration, synaptosomes were treated with saponin to disrupt the plasmalemmal permeability barrier. When these synaptosomes were incubated in solutions containing Ca, ATP, and oxalate, electrondense Ca oxalate deposits were found in intraterminal mitochondria, SER cisterns, and large vesicular profiles. Saponin-treated synaptosomes that were incubated in the presence of mitochondrial poisons contained electron-dense deposits within SER cisterns and large vesicular profiles, but very rarely in mitochondria. Similar deposits were observed within saponin-treated synaptosomes that were not post-fixed with OSO4, and within saponin-treated synaptosomes that were prepared for analysis by freeze-substitution. Electron-probe microanalyses of these deposits confirmed the presence of large concentrations of Ca. When oxalate was omitted from the incubation solutions, no electron-dense deposits were present in saponin-treated synaptosomes. In other control experiments, either the Ca ionophore A23187 or the Ca chelator EGTA was added to the incubation media; electron-dense deposits were very rarely observed within the intraterminal organelles of these saponin-treated synaptosomes. The data indicate that presynaptic nerve terminal SER is indeed a Ca-sequestering organelle.

摘要

运用超微结构技术和电子探针微量分析来确定突触前神经终末内的滑面内质网(SER)是否为钙螯合位点。SER的三维结构由突触体的连续切片确定。SER由扁平的池组成,这些池可能分支并经常与线粒体并列。为了研究终末内的钙螯合,用皂角苷处理突触体以破坏质膜通透性屏障。当这些突触体在含有钙、ATP和草酸盐的溶液中孵育时,在终末内的线粒体、SER池和大泡状结构中发现了电子致密的草酸钙沉淀。在存在线粒体毒物的情况下孵育的经皂角苷处理的突触体,其SER池和大泡状结构内含有电子致密沉淀,但线粒体中很少见。在未用四氧化锇后固定的经皂角苷处理的突触体中,以及在通过冷冻置换制备用于分析的经皂角苷处理的突触体中,观察到了类似的沉淀。对这些沉淀的电子探针微量分析证实了大量钙的存在。当孵育溶液中省略草酸盐时,经皂角苷处理的突触体中不存在电子致密沉淀。在其他对照实验中,将钙离子载体A23187或钙螯合剂乙二醇双乙醚二胺四乙酸(EGTA)添加到孵育培养基中;在这些经皂角苷处理的突触体的终末内细胞器中很少观察到电子致密沉淀。数据表明突触前神经终末SER确实是一种钙螯合细胞器。

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