Meyer A C, Neher E, Schneggenburger R
Max-Planck-Institut für biophysikalische Chemie, Abteilung Membranbiophysik, D-37077 Göttingen, Germany.
J Neurosci. 2001 Oct 15;21(20):7889-900. doi: 10.1523/JNEUROSCI.21-20-07889.2001.
At the large excitatory calyx of Held synapse, the quantal size during an evoked EPSC and the number of active zones contributing to transmission are not known. We developed a nonstationary variant of EPSC fluctuation analysis to determine these quantal parameters. AMPA receptor-mediated EPSCs were recorded in slices of young (postnatal 8-10 d) rats after afferent fiber stimulation, delivered in trains to induce synaptic depression. The means and the variances of EPSC amplitudes were calculated across trains for each stimulus number. During 10 Hz trains at 2 mm Ca(2+) concentration ([Ca(2+)]), we found linear EPSC variance-mean relationships, with a slope that was in good agreement with the quantal size obtained from amplitude distributions of spontaneous miniature EPSCs. At high release probability with 10 or 15 mm [Ca(2+)], competitive antagonists were used to partially block EPSCs. Under these conditions, the EPSC variance-mean plots could be fitted with parabolas, giving estimates of quantal size and of the binomial parameter N. With the rapidly dissociating antagonist kynurenic acid, quantal sizes were larger than with a slowly dissociating antagonist, suggesting that the effective glutamate concentration was increased at high release probability. Considering the possibility of multivesicular release and moderate saturation of postsynaptic AMPA receptors, we conclude that the binomial parameter N (637 +/- 117; mean +/- SEM) represents an upper limit estimate of the number of functional active zones. We estimate that during normal synaptic transmission, the probability of vesicle fusion at single active zones is in the range of 0.25-0.4.
在大型兴奋性海氏突触中,诱发的兴奋性突触后电流(EPSC)期间的量子大小以及对传递有贡献的活性区数量尚不清楚。我们开发了一种EPSC波动分析的非平稳变体来确定这些量子参数。在传入纤维刺激后,记录幼龄(出生后8 - 10天)大鼠脑片上由α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体介导的EPSC,以串刺激诱发突触抑制。计算每个刺激次数下各串EPSC幅度的均值和方差。在2 mM钙离子浓度([Ca²⁺])下以10 Hz串刺激时,我们发现EPSC方差-均值呈线性关系,其斜率与从自发微小EPSC幅度分布获得的量子大小高度一致。在10或15 mM [Ca²⁺]的高释放概率条件下,使用竞争性拮抗剂部分阻断EPSC。在这些条件下,EPSC方差-均值图可拟合为抛物线,从而得到量子大小和二项式参数N的估计值。使用快速解离的拮抗剂犬尿氨酸时,量子大小比使用缓慢解离的拮抗剂时更大,这表明在高释放概率下有效谷氨酸浓度增加。考虑到多泡释放的可能性以及突触后AMPA受体的适度饱和,我们得出结论,二项式参数N(637 ± 117;均值 ± 标准误)代表功能性活性区数量的上限估计值。我们估计在正常突触传递过程中,单个活性区囊泡融合的概率在0.25 - 0.4范围内。