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钙在去极化-分泌偶联中的作用:利用水母发光蛋白对鱿鱼巨大突触的研究

Calcium role in depolarization-secretion coupling: an aequorin study in squid giant synapse.

作者信息

Llinás R, Nicholson C

出版信息

Proc Natl Acad Sci U S A. 1975 Jan;72(1):187-90. doi: 10.1073/pnas.72.1.187.

Abstract

Aequorin, a protein that emits light in the presence of calcium, was injected in the presynaptic terminal of the squid giant synapse. This injection was preceded by intracellular tetraethylammonium administration, which prolonged the duration of the presynaptic action potential. After this procedure light emission was evoked by single presynaptic spikes capable of releasing synaptic transmitter. In a second set of experiments, presynaptic tetraethylammonium injection was followed by the administration of tetrodotoxin extracellularly, which abolished the presynaptic action potential. Under these conditions artificial depolarization of the presynaptic terminal triggered the release of synaptic transmitter, in a graded manner. However, as previously reported by other authors, membrane potential steps to an internal positive value of approximately plus 90 mV (the suppression potential) produced a blockage of transmitter release for the duration of the imposed potential. Synaptic transmission recurred, nevertheless, as the current injection was terminated. A similar set of experiments, performed after the intracellular injection of aequorin in the presynaptic fiber, demonstrated that the aequorin light response was evoked by membrane potential steps capable of releasing synaptic transmitter. If the membrane potential was made positive to the "suppression" level, no light response was evoked but the light emission appeared, as did transmitter release, at the end of the current pulse. These experiments demonstrate that release of transmitter is directly correlated with intracellular calcium concentration and that the suppression potential is compatible with the existence of a calcium equilibrium potential at the presynaptic terminal.

摘要

水母发光蛋白是一种在钙存在时会发光的蛋白质,被注射到枪乌贼巨大突触的突触前终末。在进行这种注射之前,先进行了细胞内注射四乙铵,这延长了突触前动作电位的持续时间。在此操作之后,能够释放突触递质的单个突触前尖峰诱发了发光。在第二组实验中,在突触前注射四乙铵之后,在细胞外施加河豚毒素,这消除了突触前动作电位。在这些条件下,突触前终末的人工去极化以分级方式触发了突触递质的释放。然而,正如其他作者先前报道的那样,膜电位跃升至约 +90 mV 的内部正值(抑制电位)会在施加电位的持续时间内导致递质释放受阻。不过,随着电流注射的终止,突触传递再次出现。在突触前纤维中进行水母发光蛋白的细胞内注射后进行的一组类似实验表明,能够释放突触递质的膜电位跃变诱发了水母发光蛋白的光反应。如果膜电位变为正值达到“抑制”水平,则不会诱发光反应,但在电流脉冲结束时会出现发光现象,递质释放也是如此。这些实验表明,递质的释放与细胞内钙浓度直接相关,并且抑制电位与突触前终末存在钙平衡电位是相符的。

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