Hvalby Øivind, Jensen Vidar, Kao Hung-Teh, Walaas S Ivar
Molecular Neurobiology Research Group, Institute of Basic Medical Sciences, University of Oslo, PO Box 1103 Blindern, 0317 Oslo, Norway.
J Physiol. 2006 Feb 15;571(Pt 1):75-82. doi: 10.1113/jphysiol.2005.100685. Epub 2005 Dec 1.
The effects of synapsin proteins on synaptic transmission from vesicles in the readily releasable vesicle pool have been examined by comparing excitatory synaptic transmission in hippocampal slices from mice devoid of synapsins I and II and from wild-type control animals. Application of stimulus trains at variable frequencies to the CA3-to-CA1 pyramidal cell synapse suggested that, in both genotypes, synaptic responses obtained within 2 s stimulation originated from readily releasable vesicles. Detailed analysis of the responses during this period indicated that stimulus trains at 2-20 Hz enhanced all early synaptic responses in the CA3-to-CA1 pyramidal cell synapse, but depressed all early responses in the medial perforant path-to-granule cell synapse. The synapsin-dependent part of these responses, i.e. the difference between the results obtained in the transgene and the wild-type preparations, showed that in the former synapse, the presence of synapsins I and II minimized the early responses at 2 Hz, but enhanced the early responses at 20 Hz, while in the latter synapse, the presence of synapsins I and II enhanced all responses at both stimulation frequencies. The results indicate that synapsins I and II are necessary for full expression of both enhancing and decreasing modulatory effects on synaptic transmission originating from the readily releasable vesicles in these excitatory synapses.
通过比较缺乏突触结合蛋白I和II的小鼠海马切片与野生型对照动物海马切片中的兴奋性突触传递,研究了突触结合蛋白对来自易释放囊泡池的囊泡突触传递的影响。以可变频率向CA3至CA1锥体细胞突触施加刺激串表明,在两种基因型中,2秒刺激内获得的突触反应均源自易释放囊泡。对这一时期反应的详细分析表明,2-20Hz的刺激串增强了CA3至CA1锥体细胞突触中的所有早期突触反应,但抑制了内侧穿通通路至颗粒细胞突触中的所有早期反应。这些反应中依赖突触结合蛋白的部分,即在转基因制剂和野生型制剂中获得的结果之间的差异,表明在前一种突触中,突触结合蛋白I和II的存在使2Hz时的早期反应最小化,但增强了20Hz时的早期反应,而在后一种突触中,突触结合蛋白I和II的存在增强了两种刺激频率下的所有反应。结果表明,突触结合蛋白I和II对于充分表达对源自这些兴奋性突触中易释放囊泡的突触传递的增强和减弱调节作用是必需的。