Overstreet Linda S, Westbrook Gary L
Vollum Institute, Oregon Health & Science University, Portland, Oregon 97201, USA.
J Neurosci. 2003 Apr 1;23(7):2618-26. doi: 10.1523/JNEUROSCI.23-07-02618.2003.
Neurotransmitter transporters may promote synapse specificity by limiting spillover between release sites. At GABAergic synapses, transport block prolongs synaptic responses when many inputs are activated, yet it is unclear whether transporters alter signaling by single axons. We found that unitary IPSCs generated by paired recordings between hippocampal interneurons and granule cells could be either prolonged or totally unaffected by block of GABA transporters. This variability was explained by the density of active release sites rather than the number of active sites. Prolongation by transport block required release from multiple sites and was enhanced by repetitive activation. Furthermore, transport-sensitive unitary IPSCs were accelerated when the release probability was reduced, indicating that cross talk prolonged the time course of IPSCs even when transport was intact. Our results suggest that the release site density regulates the degree of cross talk as well as the contribution of transporters to GABA clearance. Thus, interplay between release site density and transporter action determines the independence of unitary inhibitory synapses.
神经递质转运体可能通过限制释放位点之间的递质外溢来促进突触特异性。在GABA能突触中,当多个输入被激活时,转运体阻断会延长突触反应,但目前尚不清楚转运体是否会改变单个轴突的信号传递。我们发现,海马中间神经元与颗粒细胞之间通过配对记录产生的单位IPSC,可能会因GABA转运体的阻断而延长,也可能完全不受影响。这种变异性可以用活跃释放位点的密度而非活跃位点的数量来解释。转运体阻断导致的延长需要多个位点释放递质,并且通过重复激活会增强。此外,当释放概率降低时,对转运体敏感的单位IPSC会加速,这表明即使转运体功能正常,串扰也会延长IPSC的时间进程。我们的结果表明,释放位点密度调节串扰程度以及转运体对GABA清除的贡献。因此,释放位点密度与转运体作用之间的相互作用决定了单位抑制性突触的独立性。