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突触元件形成所需的蛋白质合成

Protein synthesis requirement for the formation of synaptic elements.

作者信息

Burry R W

出版信息

Brain Res. 1985 Sep 30;344(1):109-19. doi: 10.1016/0006-8993(85)91194-1.

Abstract

The formation of synapses in cell cultures of rat cerebellum was examined in the presence of the protein synthesis inhibitor cycloheximide. First, cell survival in the presence of 25 micrograms/ml cycloheximide was determined by phase contrast microscopy, trypan blue exclusion, total protein and uptake of [3H]gamma-aminobutyric acid (GABA). Neurons with 24 h incubation in cycloheximide appeared normal with little cell death, but by 48 h incubation the first signs of cell death were found. Some viable neurons were still found in cultures incubated continuously in cycloheximide for 72 h. Normally, the number of synapses seen in cerebellar cultures with the electron microscope shows an increase during the first several weeks in culture. However, the number of synapses in cultures treated with cycloheximide decreased, indicating that inhibition of protein synthesis at least partially inhibited synaptogenesis. Cycloheximide also inhibited the maintenance of synapses already formed as seen by the decrease in the number of synapses from the time the cycloheximide was added. To determine the sensitivity of the forming presynaptic element to cycloheximide, the development of apparent presynaptic elements was investigated. In cultures treated with polylysine-coated sepharose beads, neurites grew and formed apparent presynaptic elements with the bead taking the position of the postsynaptic element. Cultures pretreated with cycloheximide for 1 h followed by 24 h incubation with both cycloheximide and coated beads showed a normal number of apparent presynaptic elements. The first decrease in numbers was seen after 12 h preincubation and 12 h incubation with both cycloheximide and coated beads. Even after 72 h continuous incubation some apparent presynaptic elements could be formed although at reduced levels. Results presented here suggest that continuous protein synthesis is not necessary for the formation of the presynaptic element, but that active protein synthesis is required for neurons to form and maintain postsynaptic elements.

摘要

在蛋白质合成抑制剂环己酰亚胺存在的情况下,对大鼠小脑细胞培养物中突触的形成进行了研究。首先,通过相差显微镜、台盼蓝排斥法、总蛋白以及[3H]γ-氨基丁酸(GABA)摄取来测定在25微克/毫升环己酰亚胺存在下的细胞存活率。在环己酰亚胺中孵育24小时的神经元看起来正常,几乎没有细胞死亡,但在孵育48小时时发现了细胞死亡的最初迹象。在连续用环己酰亚胺孵育72小时的培养物中仍发现一些存活的神经元。正常情况下,用电镜观察小脑培养物中可见的突触数量在培养的最初几周内会增加。然而,用环己酰亚胺处理的培养物中的突触数量减少,这表明蛋白质合成的抑制至少部分抑制了突触发生。环己酰亚胺还抑制了已形成突触的维持,从添加环己酰亚胺时起突触数量的减少就可以看出这一点。为了确定正在形成的突触前元件对环己酰亚胺的敏感性,研究了明显突触前元件的发育情况。在用聚赖氨酸包被的琼脂糖珠处理的培养物中,神经突生长并形成明显的突触前元件,珠子占据突触后元件的位置。先用环己酰亚胺预处理1小时,然后用环己酰亚胺和包被珠子共同孵育24小时的培养物显示出正常数量的明显突触前元件。在预孵育12小时并与环己酰亚胺和包被珠子共同孵育12小时后,数量首次减少。即使连续孵育72小时,仍可形成一些明显的突触前元件,尽管水平有所降低。此处呈现的结果表明,持续的蛋白质合成对于突触前元件的形成不是必需的,但活跃的蛋白质合成对于神经元形成和维持突触后元件是必需的。

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