Wojtowicz J M, Marin L, Atwood H L
Department of Physiology, University of Toronto, Ontario, Canada.
J Neurosci. 1994 Jun;14(6):3688-703. doi: 10.1523/JNEUROSCI.14-06-03688.1994.
Crustacean motor axons provide a model in which activity-dependent changes in synaptic physiology and synaptic structure can be concurrently observed in single identifiable neurons. In response to a train of stimulation, crustacean neuromuscular junctions undergo pronounced facilitation of transmitter release. The effects of maintained high-frequency stimulation may persist for at least several hours ("long-term facilitation"). Electrophysiological studies suggest that the number of "active" synapses contributing transmitter quanta at low frequencies of stimulation increases during and after a train of high-frequency stimulation. However, at different terminal recording sites the effect of stimulation varies, and it was observed that not all released quanta produce a voltage change in the postsynaptic muscle cell. Electron microscopic examinations of serial sections from nerve terminals subjected to stimulation were made to determine whether changes in synaptic structure could be correlated with activity-induced long-lasting enhancement of transmission. A procedure was introduced for marking a recorded terminal with fluorescent polystyrene microspheres, which are visible in electron micrographs of the recording site. Crustacean nerve terminals possess a large number of discrete synapses, a small fraction of which have multiple presynaptic "active zones" (dense bodies with clustered synaptic vesicles, thought to represent sites of evoked transmitter release). In terminals previously stimulated, the proportion of synapses with multiple "active zones" is greater than in control unstimulated terminals. Total synaptic vesicle counts and readily releasable vesicles at synapses are not significantly different in previously stimulated terminals and controls. In terminals fixed during stimulation a few synapses show evidence of division in "active zones," and synaptic vesicle counts are lower than in controls.(ABSTRACT TRUNCATED AT 250 WORDS)
甲壳类动物的运动轴突提供了一个模型,在这个模型中,可以在单个可识别的神经元中同时观察到突触生理学和突触结构中依赖于活动的变化。响应一连串的刺激,甲壳类动物的神经肌肉接头会经历递质释放的显著易化。持续高频刺激的影响可能会持续至少几个小时(“长期易化”)。电生理学研究表明,在一连串高频刺激期间及之后,在低频刺激时贡献递质量子的“活跃”突触数量会增加。然而,在不同的终末记录部位,刺激的效果有所不同,并且观察到并非所有释放的量子都会在突触后肌肉细胞中产生电压变化。对受刺激神经终末的连续切片进行电子显微镜检查,以确定突触结构的变化是否与活动诱导的持久传递增强相关。引入了一种用荧光聚苯乙烯微球标记记录终末的方法,这些微球在记录部位的电子显微照片中可见。甲壳类动物的神经终末拥有大量离散的突触,其中一小部分具有多个突触前“活跃区”(带有成簇突触小泡的致密体,被认为代表诱发递质释放的部位)。在先前受刺激的终末中,具有多个“活跃区”的突触比例高于未受刺激的对照终末。在先前受刺激的终末和对照终末中,突触小泡总数和突触处易于释放的小泡数量没有显著差异。在刺激期间固定的终末中,一些突触显示出“活跃区”分裂的迹象,并且突触小泡数量低于对照终末。(摘要截取自250字)