Paired-pulse plasticity at the single release site level: An experimental and computational study

被引:55
作者
Hanse, E [1 ]
Gustafsson, B [1 ]
机构
[1] Univ Gothenburg, Inst Physiol & Pharmacol, SE-40530 Gothenburg, Sweden
关键词
paired pulse; release probability; hippocampus; CA1; synaptic plasticity; development;
D O I
10.1523/JNEUROSCI.21-21-08362.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
CA3-CA1 glutamatergic synapses in the hippocampus exhibit a large heterogeneity in release probability (p) and paired-pulse (PP) plasticity, established already in the early neonatal period when the CA3-CA1 connections consist of only a single release site. At such a site two factors decide initial release probability: the number of immediately releasable vesicles (preprimed pool) and the vesicle release probability (P-ves1). Depletion and replenishment of this pool, an alteration in P-ves, and desensitization of postsynaptic receptors may contribute to PP plasticity. A model based on data from single neonatal CA3-CA1 synapses has been used to address the relative importance of these factors for the heterogeneity in PP plasticity. At a 20 msec PP interval, the PP ratio (P-2/P-1) varied from 0.1 to 4.5 among the synapses. At this interval desensitization and replenishment were of little importance. The heterogeneity was explained mostly by the variation in P-ves1, whereas the preprimed pool size was of minor importance. P-ves altered from the first to the second stimulus such that P-ves2 was rather uniform among the synapses. Its variation thus contributed little to the heterogeneity in PP ratio. The model also shows that the relationship between alterations in release probability and PP ratio is complex. Thus, an increase in release probability can be associated with an increase, a decrease, or no change at all in PP ratio, depending on the original values of P-ves1 and the preprimed pool and on which one of these factors is altered to produce the increase in release probability.
引用
收藏
页码:8362 / 8369
页数:8
相关论文
共 27 条
[21]   TRANSMISSION AT A CENTRAL INHIBITORY SYNAPSE .3. ULTRASTRUCTURE OF PHYSIOLOGICALLY IDENTIFIED AND STAINED TERMINALS [J].
TRILLER, A ;
KORN, H .
JOURNAL OF NEUROPHYSIOLOGY, 1982, 48 (03) :708-736
[22]   Dissection of three Ca2+-dependent steps leading to secretion in chromaffin cells from mouse adrenal slices [J].
Voets, T .
NEURON, 2000, 28 (02) :537-545
[23]   Properties and plasticity of paired-pulse depression at a central synapse [J].
Waldeck, RF ;
Pereda, A ;
Faber, DS .
JOURNAL OF NEUROSCIENCE, 2000, 20 (14) :5312-5320
[24]   The reduced release probability of releasable vesicles during recovery from short-term synaptic depression [J].
Wu, LG ;
Borst, JGG .
NEURON, 1999, 23 (04) :821-832
[25]   Transport, capture and exocytosis of single synaptic vesicles at active zones [J].
Zenisek, D ;
Steyer, JA ;
Almers, W .
NATURE, 2000, 406 (6798) :849-854
[26]   Assembling the presynaptic active zone: A characterization of an active zone precursor vesicle [J].
Zhai, RG ;
Vardinon-Friedman, H ;
Cases-Langhoff, C ;
Becker, B ;
Gundelfinger, ED ;
Ziv, NE ;
Garner, CC .
NEURON, 2001, 29 (01) :131-143
[27]  
ZUCKER RS, 1989, ANNU REV NEUROSCI, V12, P13, DOI 10.1146/annurev.neuro.12.1.13