Ikeda Kaori, Bekkers John M
Division of Neuroscience, John Curtin School of Medical Research, Australian National University, Canberra, ACT 0200, Australia.
Proc Natl Acad Sci U S A. 2009 Feb 24;106(8):2945-50. doi: 10.1073/pnas.0811017106. Epub 2009 Feb 6.
Synaptic transmission depends on the continued availability of neurotransmitter-filled synaptic vesicles (SVs) for triggered release from presynaptic boutons. Surprisingly, small boutons in the brain, that already contain comparatively few SVs, are thought to retain the majority of these SVs in a "reserve" pool that is not mobilized under physiological conditions. Why such a scarce synaptic resource is normally inaccessible has been a matter of debate. Here, we readdress this issue by developing an electrophysiological approach for counting SVs released from boutons formed by a single, isolated neuron on itself ("autapses"). We show that, after treatment with Bafilomycin A1 to prevent reloading of discharged SVs with glutamate, each SV is counted only once on first-time release. Hence, by integrating all autaptic currents as they run down over time, we can estimate the total number of SVs released by a single neuron. This total can be normalized to the number of boutons on the neuron, giving the mean number of SVs released per bouton. We estimate that up to approximately 130 vesicles can be released per bouton over approximately 10 min of stimulation at 0.2 Hz. This number of vesicles represents a substantial proportion of the total number of SVs (100-200) that have been counted in these boutons by using electron microscopy. Thus, mild electrical stimulation, when maintained for sufficient time, causes the eventual release of many of the SVs in a bouton, including those in the putative reserve pool. This result suggests that SVs are functionally homogeneous in that the majority can contribute to basal synaptic transmission.
突触传递依赖于充满神经递质的突触小泡(SVs)持续存在,以便从突触前终扣触发释放。令人惊讶的是,大脑中那些已经含有相对较少SVs的小终扣,被认为将这些SVs的大部分保留在一个“储备”池中,该储备池在生理条件下不会被动员。为什么这样一种稀缺的突触资源通常无法被利用一直是一个有争议的问题。在这里,我们通过开发一种电生理学方法来重新探讨这个问题,该方法用于计算由单个孤立神经元自身形成的终扣(“自突触”)释放的SVs数量。我们表明,在用巴弗洛霉素A1处理以防止释放的SVs重新装载谷氨酸后,每个SV在首次释放时仅被计数一次。因此,通过整合所有自突触电流随时间的衰减情况,我们可以估计单个神经元释放的SVs总数。这个总数可以相对于神经元上的终扣数量进行归一化,从而得到每个终扣释放的SVs平均数。我们估计,在0.2 Hz的刺激下持续约10分钟,每个终扣最多可释放约130个小泡。这个小泡数量占通过电子显微镜在这些终扣中计数的SVs总数(100 - 200个)的很大比例。因此,温和的电刺激在持续足够长的时间后,会导致终扣中许多SVs最终释放,包括那些在假定储备池中的SVs。这一结果表明,SVs在功能上是同质的,因为大多数SVs都可以参与基础突触传递。