Wu L G, Saggau P
Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030.
J Neurosci. 1994 Feb;14(2):645-54. doi: 10.1523/JNEUROSCI.14-02-00645.1994.
We examined the relationship between presynaptic calcium levels and postsynaptic potentials during normal synaptic transmission, paired-pulse facilitation (PPF), and long-term potentiation (LTP) in CA3-CA1 synapses of hippocampus. By selectively loading the presynaptic terminals with the calcium indicator fura-2, we simultaneously recorded a presynaptic calcium (Ca) transient and the corresponding field EPSP evoked by a single stimulus given to the Schaffer collateral-commissural pathway in guinea pig hippocampal slices. A volume average presynaptic Ca influx was obtained by taking the first time derivative of the Ca transient. Our data indicate that the synaptic transmission represented by the initial slope of the field EPSP is approximately proportional to the fourth power of the presynaptic Ca influx, the volume average Ca current. Our results in combination with similar findings at the squid giant synapse (Augustine et al., 1985b; Augustine and Charlton, 1986) suggest that the relationship between Ca influx and transmitter release is well conserved from the molluscan to the mammalian nervous system. A transient increase of the residual Ca level ([Ca]res) is generally thought to be the mechanism underlying PPF (Katz and Miledi, 1968; Charlton et al., 1982); however, the relationship between PPF and the presynaptic [Ca]res had not been examined before. Our results demonstrate that PPF is approximately linearly related to the [Ca]res. This finding further supports the residual Ca hypothesis for PPF. Accumulated evidence from other groups suggests that the presynaptic site contributes to the maintenance of LTP in CA3-CA1 synapses (Bekkers and Stevens, 1990; Malinow and Tsien, 1990); however, our data show that neither an increase of the Ca transient nor a sustained increase of the [Ca]res occurs in the presynaptic terminals during maintenance of LTP. This suggests that the presynaptic mechanism underlying LTP must be downstream to Ca influx.
我们研究了海马体CA3-CA1突触在正常突触传递、双脉冲易化(PPF)和长时程增强(LTP)过程中突触前钙水平与突触后电位之间的关系。通过用钙指示剂fura-2选择性地加载突触前终末,我们同时记录了豚鼠海马切片中施万细胞侧支-联合通路给予单个刺激所诱发的突触前钙(Ca)瞬变和相应的场兴奋性突触后电位(fEPSP)。通过对Ca瞬变进行一阶时间导数运算,获得了体积平均突触前Ca内流。我们的数据表明,由场兴奋性突触后电位初始斜率所代表的突触传递与突触前Ca内流(体积平均Ca电流)的四次方大致成正比。我们的结果与乌贼巨突触的类似发现(Augustine等人,1985b;Augustine和Charlton,1986)相结合,表明从软体动物到哺乳动物神经系统,Ca内流与递质释放之间的关系得到了很好的保留。残余钙水平([Ca]res)的短暂升高通常被认为是双脉冲易化的潜在机制(Katz和Miledi,1968;Charlton等人,1982);然而,双脉冲易化与突触前[Ca]res之间的关系此前尚未得到研究。我们的结果表明,双脉冲易化与[Ca]res大致呈线性关系。这一发现进一步支持了双脉冲易化的残余钙假说。其他研究小组积累的证据表明,突触前位点有助于CA3-CA1突触长时程增强的维持(Bekkers和Stevens,1990;Malinow和Tsien,1990);然而,我们的数据表明,在长时程增强维持期间,突触前终末既没有出现Ca瞬变增加,也没有出现[Ca]res持续增加。这表明长时程增强的突触前机制一定位于Ca内流的下游。