Presynaptic Ca2+ requirements and developmental regulation of posttetanic Potentiation at the calyx of Held

被引:79
作者
Korogod, N
Lou, XL
Schneggenburger, R
机构
[1] Max Planck Inst Biophys Chem, AG Synapt Dynam & Modulat, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Abt Membranbiophys, D-37077 Gottingen, Germany
关键词
synaptic plasticity; nerve terminal; transmitter release; release probability; calcium; imaging;
D O I
10.1523/JNEUROSCI.1295-05.2005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Large excitatory synapses in the auditory system, such as the calyx of Held, faithfully transmit trains of action potentials up to a frequency of a few hundred hertz, and these synapses are thought to display a limited repertoire of synaptic plasticity. Here, we show that brief trains of 100 Hz stimulation induce posttetanic potentiation (PTP) of transmitter release at the calyx of Held. In young rats [ postnatal day 4 (P4) to P6], PTP could be induced with shorter 100 Hz trains compared with older age groups (P8 - P10 and P12 - P14), but the maximal amount of PTP was similar, with similar to 200% of control EPSC amplitude. The size of the readily releasable pool of vesicles was not increased significantly during PTP. Bath application of the membrane-permeable Ca2+ chelator EGTA-AM suppressed PTP, indicating a role for presynaptic Ca2+ in PTP at the calyx of Held. Presynaptic Ca2+ imaging showed that the intracellular Ca2+ concentration, [Ca2+](i), was increased by 40 - 120 nM at the peak of PTP, and this "residual" [Ca2+](i) decayed in parallel with PTP, with time constants in the range of 10 - 60 s. During whole-cell recording of the presynaptic calyx of Held, PTP was absent, and the decay of residual [Ca2+](i) was strongly accelerated. The data show that the calyx of Held expresses a mechanism of transmitter release potentiation in which a small, sustained elevation of basal [Ca2+](i) increases the transmitter release probability after trains of high-frequency stimulation.
引用
收藏
页码:5127 / 5137
页数:11
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