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突触形成对培养的水蛭神经元钙电流和神经突生长的顺行和逆行影响。

Anterograde and retrograde effects of synapse formation on calcium currents and neurite outgrowth in cultured leech neurons.

作者信息

Cooper R L, Fernández-de-Miguel F, Adams W B, Nicholls J G

机构信息

Department of Pharmacology, Biocenter, University of Basle, Switzerland.

出版信息

Proc Biol Sci. 1992 Aug 22;249(1325):217-22. doi: 10.1098/rspb.1992.0107.

Abstract

The aim of our experiments has been to analyse how formation of chemical synapses affects the distribution of calcium (Ca2+) currents and neurite outgrowth of leech Retzius cells. Previous results showed that Ca2+ currents measured in the initial process or 'stump' of postsynaptic cells were significantly smaller than those in corresponding sites on presynaptic neurons. In the present experiments, neurons were plated together in close apposition as pairs or as triads, with the tip of one Retzius cell touching the soma of another. Ca2+ currents from selected areas of the neuronal surfaces were measured by loose-patch recording before and after the formation of chemically mediated synaptic connections, which developed in about 8 h. With three cells arranged in a row, the last of the series, which was purely postsynaptic (i.e. with no target), also showed a dramatic reduction in Ca2+ currents in its initial segment, compared with the currents seen in either the first cell (purely presynaptic) or the second cell of the chain (which was both postsynaptic to the first cell and presynaptic to the third). This suggests that retrograde as well as anterograde effects on Ca2+ currents occurred as a result of synapse formation: the Ca2+ currents in the middle cell did not decrease although a synapse had been formed on it. To test for additional consequences of synapse formation, neurite outgrowth was measured in postsynaptic cells and in single cells plated on an extract of extracellular matrix containing laminin (ECM-laminin). After 48 h, the total length of neuritic outgrowth in postsynaptic cells was only about one third of that in single cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们实验的目的是分析化学突触的形成如何影响钙(Ca2+)电流的分布以及水蛭雷特修斯细胞的神经突生长。先前的结果表明,在突触后细胞的初始过程或“残端”中测量到的Ca2+电流明显小于突触前神经元相应部位的电流。在本实验中,神经元成对或成三联体紧密并列培养,一个雷特修斯细胞的尖端接触另一个细胞的胞体。在化学介导的突触连接形成前后(约8小时形成),通过松散膜片钳记录测量神经元表面选定区域的Ca2+电流。当三个细胞排成一排时,系列中的最后一个细胞,即纯粹的突触后细胞(即没有靶细胞),与第一个细胞(纯粹的突触前细胞)或链中的第二个细胞(既是第一个细胞的突触后细胞,又是第三个细胞的突触前细胞)相比,其初始段的Ca2+电流也显著降低。这表明突触形成导致了对Ca2+电流的逆行和顺行效应:中间细胞上虽然形成了突触,但其Ca2+电流并未降低。为了测试突触形成的其他后果,在突触后细胞和接种在含有层粘连蛋白的细胞外基质提取物(ECM-层粘连蛋白)上的单细胞中测量神经突生长。48小时后,突触后细胞中神经突生长的总长度仅约为单细胞中的三分之一。(摘要截短至250字)

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