Msghina M, Millar A G, Charlton M P, Govind C K, Atwood H L
Department of Physiology, Medical Research Council Neural Group, University of Toronto, Toronto, Ontario, Canada M5S 1A8.
J Neurosci. 1999 Oct 1;19(19):8419-34. doi: 10.1523/JNEUROSCI.19-19-08419.1999.
Synaptic functional differentiation of crayfish phasic and tonic motor neurons is large. For one impulse, quantal release of neurotransmitter is typically 100-1000 times higher for phasic synapses. We tested the hypothesis that differences in synaptic strength are determined by differences in synaptic calcium entry. Calcium signals were measured with the injected calcium indicator dyes Calcium Green-1 and fura-2. Estimated Ca(2+) entry increased almost linearly with frequency for both axons and was two to three times larger in phasic terminals. Tonic terminal Ca(2+) at 10 Hz exceeded phasic terminal Ca(2+) at 1 Hz, yet transmitter release was much higher for phasic terminals at these frequencies. Freeze-fracture images of synapses revealed on average similar numbers of prominent presynaptic active zone particles (putative ion channels) for both neurons and a two- to fourfold phasic/tonic ratio of active zones per terminal volume. This can account for the larger calcium signals seen in phasic terminals. Thus, differences in synaptic strength are less closely linked to differences in synaptic channel properties and calcium entry than to differences in calcium sensitivity of transmitter release.
小龙虾相位性和紧张性运动神经元的突触功能分化程度很大。对于单个冲动,相位性突触中神经递质的量子释放通常要高出100 - 1000倍。我们检验了这样一个假说,即突触强度的差异是由突触钙内流的差异所决定的。使用注射的钙指示剂染料钙黄绿素 - 1和fura - 2来测量钙信号。估计的Ca(2+)内流对于轴突来说几乎随频率呈线性增加,并且在相位性终末中要大两到三倍。10Hz时紧张性终末的Ca(2+)超过了1Hz时相位性终末的Ca(2+),然而在这些频率下相位性终末的递质释放要高得多。突触的冷冻蚀刻图像显示,这两种神经元的突触前活跃区颗粒(假定的离子通道)平均数量相似,并且每个终末体积的活跃区相位性/紧张性比例为两到四倍。这可以解释在相位性终末中看到的更大的钙信号。因此,突触强度的差异与突触通道特性和钙内流的差异的关联程度,低于与递质释放的钙敏感性差异的关联程度。