What We Can Learn From Cumulative Numbers of Vesicular Release Events

被引:5
作者
Miki, Takafumi [1 ]
机构
[1] Doshisha Univ, Grad Sch Brain Sci, Kyoto, Japan
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2019年 / 13卷
基金
日本学术振兴会;
关键词
synapse; neurotransmitter release; quantal analysis; release site; vesicle recruitment; SYNAPTIC VESICLES; CELL SYNAPSES; GRANULE CELL; TRANSMISSION; NEUROTRANSMITTER; PROBABILITY; DECONVOLUTION; KINETICS; RECOVERY; SENSOR;
D O I
10.3389/fncel.2019.00257
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Following action potential invasion in presynaptic terminals, synaptic vesicles are released in a stochastic manner at release sites (docking sites). Since neurotransmission occurs at frequencies up to 1 kHz, the mechanisms underlying consecutive vesicle releases at a docking site during high frequency bursts is a key factor for understanding the role and strength of the synapse. Particularly new vesicle recruitment at the docking site during neuronal activity is thought to be crucial for short-term plasticity. However current studies have not reached a unified docking site model for central synapses. Here I review newly developed analyses that can provide insight into docking site models. Quantal analysis using counts of vesicular release events provide a wealth of information not only to monitor the number of docking sites, but also to distinguish among docking site models. The stochastic properties of cumulative release number during bursts allow us to estimate the total number of releasable vesicles and to deduce the features of vesicle recruitment at docking sites and the change of release probability during bursts. This analytical method may contribute to a comprehensive understanding of release/replenishment mechanisms at a docking site.
引用
收藏
页数:8
相关论文
共 51 条
  • [1] Fast, Automated Implementation of Temporally Precise Blind Deconvolution of Multiphasic Excitatory Postsynaptic Currents
    Andor-Ardo, Daniel
    Keen, Erica C.
    Hudspeth, A. J.
    Magnasco, Marcelo O.
    [J]. PLOS ONE, 2012, 7 (06):
  • [2] Atluri PP, 1998, J NEUROSCI, V18, P8214
  • [3] Heterogeneity of functional synaptic parameters among single release sites
    Auger, C
    Marty, A
    [J]. NEURON, 1997, 19 (01) : 139 - 150
  • [4] A use-dependent increase in release sites drives facilitation at calretinin-deficient cerebellar parallel-fiber synapses
    Brachtendorf, Simone
    Eilers, Jens
    Schmidt, Hartmut
    [J]. FRONTIERS IN CELLULAR NEUROSCIENCE, 2015, 9
  • [5] Synaptotagmin-1 drives synchronous Ca2+-triggered fusion by C2B-domain-mediated synaptic-vesicle-membrane attachment
    Chang, Shuwen
    Trimbuch, Thorsten
    Rosenmund, Christian
    [J]. NATURE NEUROSCIENCE, 2018, 21 (01) : 33 - +
  • [6] Ca2+ Channel to Synaptic Vesicle Distance Accounts for the Readily Releasable Pool Kinetics at a Functionally Mature Auditory Synapse
    Chen, Zuxin
    Das, Brati
    Nakamura, Yukihiro
    DiGregorio, David A.
    Young, Samuel M., Jr.
    [J]. JOURNAL OF NEUROSCIENCE, 2015, 35 (05) : 2083 - 2100
  • [7] Detection of spontaneous synaptic events with an optimally scaled template
    Clements, JD
    Bekkers, JM
    [J]. BIOPHYSICAL JOURNAL, 1997, 73 (01) : 220 - 229
  • [8] Unveiling synaptic plasticity: a new graphical and analytical approach
    Clements, JD
    Silver, RA
    [J]. TRENDS IN NEUROSCIENCES, 2000, 23 (03) : 105 - 113
  • [9] Fast vesicle replenishment and rapid recovery from desensitization at a single synaptic release site
    Crowley, John J.
    Carter, Adam G.
    Regehr, Wade G.
    [J]. JOURNAL OF NEUROSCIENCE, 2007, 27 (20) : 5448 - 5460
  • [10] QUANTAL COMPONENTS OF THE END-PLATE POTENTIAL
    DELCASTILLO, J
    KATZ, B
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 1954, 124 (03): : 560 - 573