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通过E-PTA染色和重酶解肌球蛋白标记对大鼠脑微丝进行的超微结构研究。II. 突触。

An ultrastructural study of the microfilaments in rat brain by means of E-PTA staining and heavy meromyosin labeling. II. The synapses.

作者信息

LeBeux Y J, Willemot J

出版信息

Cell Tissue Res. 1975 Jun 27;160(1):37-68. doi: 10.1007/BF00219841.

Abstract

To identify structures involved in the translocation of the synaptic vesicles towards the presynaptic membrane, an ultrastructural study has been undertaken by means of (1) the E-PTA stain and (2) the HMM-labeling procedure. Using serial sections of E-PTA stained nervous tissue, especially those made in transversal and tangential planes, the geometric order of the presynaptic grid and of its constituents has been described in detail. It consisted of dense projections having the shape of small truncated pyramids cut parallel to their hexagonal bases which rested on the electron-lucent presynaptic membrane. The dense projections were arranged at the points of equilateral triangles. Around each dense projection, six asymmetric hexagonal holes were seen to be arrayed in an hexagonal pattern, forming thus the presynaptic sieve. From the spiny tops of the dense projections, which appeared as specialized structures of the dense material coating the inner surface of the plasma membrane at the level of the synaptic cleft, fine filaments, 40--60 A in diameter, radiated and formed a three-dimensional meshwork pervading the presynaptic bag. The dense cytoplasmic coating delineating the plasma membrane served as anchor points for these microfilaments. Upon incubation with rabbit skeletal muscle HMM the microfilaments underwent specific structural changes, consisting of: (1) a striking increase in diameter; (2) the association of periodic and polarized substructures with their surfaces. The synaptic vesicles and mitochondria were seen to be attached to the numerous HMM-decorated filaments or enmeshed in the network formed by these filaments. The actin-like filaments were anchored to the plasma membrane at many points and to the presynaptic dense projections. Following incubation in the buffer alone or in buffer HMM solutions containing Na+ pyrophosphate or ATP, no arrowheaded structures were observed. Thus, a network consisting of actin-like filaments was demonstrated in the presynaptic bag. Of particular interest was the structural relation of the actin-like filaments with the occasional, tapered myosin-like filaments. The role of the presynaptic actin-like network in the transport of synaptic vesicles towards the presynaptic membrane by a mechanism of chemomechanical transduction is discussed. In the postsynaptic dendrite or dendritic spine, a filamentous network was observed to be attached to the subsynaptic web by means of the E-PTA stain and of the HMM-labeling procedure. The occurrence of an actin-like meshwork in the postsynaptic region is suggested to produce changes in the macromolecular configuration of the postsynaptic membrane by a "mechanoenzyme" system similar to that described in the mitochondrial membrane.

摘要

为了确定参与突触小泡向突触前膜转运的结构,我们通过(1)E-PTA染色和(2)HMM标记程序进行了超微结构研究。利用E-PTA染色的神经组织连续切片,特别是横切和纵切平面的切片,详细描述了突触前网格及其组成成分的几何排列。它由密集的突起组成,这些突起呈小截顶金字塔形,平行于其六边形底面切割,位于电子透明的突触前膜上。密集的突起排列在等边三角形的顶点处。在每个密集突起周围,可以看到六个不对称的六边形孔以六边形模式排列,从而形成突触前筛。从密集突起的棘状顶端,即在突触间隙水平覆盖质膜内表面的致密物质的特化结构,直径为40 - 60埃的细丝辐射出来,形成一个贯穿突触前囊泡的三维网络。勾勒质膜的致密细胞质涂层作为这些微丝的锚定点。用兔骨骼肌HMM孵育后,微丝发生了特定的结构变化,包括:(1)直径显著增加;(2)其表面出现周期性和极化的亚结构。可以看到突触小泡和线粒体附着在许多被HMM标记的细丝上,或陷入由这些细丝形成的网络中。肌动蛋白样细丝在许多点上锚定在质膜上,并与突触前致密突起相连。在单独的缓冲液中或在含有焦磷酸钠或ATP的缓冲液HMM溶液中孵育后,未观察到箭头状结构。因此,在突触前囊中证明了一个由肌动蛋白样细丝组成的网络。特别有趣的是肌动蛋白样细丝与偶尔出现的、逐渐变细的肌球蛋白样细丝的结构关系。讨论了突触前肌动蛋白样网络在通过化学机械转导机制将突触小泡向突触前膜转运中的作用。在突触后树突或树突棘中,通过E-PTA染色和HMM标记程序观察到一个丝状网络附着在突触下网。突触后区域中肌动蛋白样网络的出现被认为通过类似于线粒体膜中描述的“机械酶”系统,使突触后膜的大分子构型发生变化。

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