首页> 外文期刊>The Journal of Physiology >A limited contribution of Ca2+ current facilitation to paired-pulse facilitation of transmitter release at the rat calyx of Held.
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A limited contribution of Ca2+ current facilitation to paired-pulse facilitation of transmitter release at the rat calyx of Held.

机译:Ca2 +电流促进对Held大鼠花萼中的发射器释放的成对脉冲促进的有限贡献。

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摘要

Recent studies have suggested that transmitter release facilitation at synapses is largely mediated by presynaptic Ca(2+) current facilitation, but the exact contribution of Ca(2+) current facilitation has not been determined quantitatively. Here, we determine the contribution of Ca(2+) current facilitation, and of an increase in the residual free Ca(2+) concentration ([Ca(2+)](i)) in the nerve terminal, to paired-pulse facilitation of transmitter release at the calyx of Held. Under conditions of low release probability imposed by brief presynaptic voltage-clamp steps, transmitter release facilitation at short interstimulus intervals (4 ms) was 227 +/- 31% of control, Ca(2+) current facilitation was 113 +/- 4% of control, and the peak residual [Ca(2+)](i) was 252 +/- 18 nm over baseline. By inferring the 'local' [Ca(2+)](i) transients that drive transmitter release during these voltage-clamp stimuli with the help of a kinetic release model, we estimate that Ca(2+) current facilitation contributes to approximately 40% to paired-pulse facilitation of transmitter release. The remaining component of facilitation strongly depends on the build-up, and on the decay of the residual free [Ca(2+)](i), but cannot be explained by linear summation of the residual free [Ca(2+)](i), and the back-calculated 'local' [Ca(2+)](i) signal, which only accounts for approximately 10% of the total release facilitation. Further voltage-clamp experiments designed to compensate for Ca(2+) current facilitation demonstrated that about half of the observed transmitter release facilitation remains in the absence of Ca(2+) current facilitation. Our results indicate that paired-pulse facilitation of transmitter release at the calyx of Held is driven by at least two distinct mechanisms: Ca(2+) current facilitation, and a mechanism independent of Ca(2+) current facilitation that closely tracks the time course of residual free [Ca(2+)](i).
机译:最近的研究表明,突触前递质释放的促进主要是由突触前的Ca(2+)电流促进介导的,但尚未定量确定Ca(2+)电流促进的确切作用。在这里,我们确定了Ca(2+)电流促进的作用以及神经末梢对成对脉冲的残余游离Ca(2+)浓度([Ca(2 +)](i))的增加。促进变送器在Held的花萼中释放。在短暂的突触前电压钳制步骤所造成的释放概率较低的情况下,在较短的刺激间隔(4毫秒)内,发射器释放的促进作用是对照组的227 +/- 31%,Ca(2+)电流的促进作用是113 +/- 4%对照,并且峰残留[Ca(2 +)](i)比基线高252 +/- 18 nm。通过推断“局部” [Ca(2 +)](i)瞬变,借助动力学释放模型在这些电压钳刺激中驱动变送器释放,我们估计Ca(2+)的电流促进作用约占40%。 %表示配对脉冲便于发射器释放。促进的剩余部分在很大程度上取决于积累,以及剩余自由[Ca(2 +)](i)的衰减,但不能通过剩余自由[Ca(2+)]的线性求和来解释。 (i),以及反向计算的“本地” [Ca(2 +)](i)信号,该信号仅占总释放促进作用的约10%。设计用于补偿Ca(2+)电流便利性的其他电压钳实验表明,在没有Ca(2+)电流便利性的情况下,大约一半的发射器释放释放便利性仍然存在。我们的结果表明,成对脉冲促进发射器释放在Held的花萼中是由至少两个不同的机制驱动的:Ca(2+)电流促进和独立于Ca(2+)电流促进的机制密切跟踪时间残余[Ca(2 +)](i)的过程。

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