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演題詳細

Poster

シナプス
Synapse

開催日 2014/9/12
時間 14:00 - 15:00
会場 Poster / Exhibition(Event Hall B)

神経伝達物質放出のタイミングを規定するカルシウムチャネルクラスターとシナプス小胞の距離
Synaptic Vesicle distance from Ca2+ channel cluster perimeter determines the time course of transmitter release at the calyx of Held

  • P2-028
  • 中村 行宏 / Yukihiro Nakamura:1 Rothman Jason S / Jason S Rothman:2 Chen Zuxin / Zuxin Chen:3 Das Brati / Brati Das:3,4 Silver Angus / Angus Silver:2 高橋 智幸 / Tomoyuki Takahashi:5,6 Young Jr Samuel M / Samuel M Young Jr:3 DiGregori David A / David A DiGregorio:1 
  • 1:Dynamic Neuronal Imaging, Dept Neuroscience, Institut Pasteur, Paris, France / Dynamic Neuronal Imaging, Dept Neuroscience, Institut Pasteur, Paris, France 2:Dept Neurosci, Physiol & Pharmacol, UCL, London, UK / Dept Neurosci, Physiol & Pharmacol, UCL, London, UK 3:Mol Mechanisms of Synaptic Func, MaxPlanck Florida Institute, Jupiter, FL, USA / Mol Mechanisms of Synaptic Func, MaxPlanck Florida Institute, Jupiter, FL, USA 4:Biol & Neurosci, Florida Atlantic Univ, Jupiter, FL, USA / Biol & Neurosci, Florida Atlantic Univ, Jupiter, FL, USA 5:同志社大院・脳科学・シナプス分子機能 / Mol Synaptic Func, Grad School of Brain Sciences, Doshisha Univ, Kyoto,Japan. 6:沖縄科学技術大学院大・細胞分子シナプス機能 / Cell & Mol Synaptic Func, Okinawa Institute of Science and Technology Grad Univ 

To encode fast auditory signals in the auditory brainstem, the reliable and synchronized transmitter release from presynaptic terminals is critical. At the calyx of Held synapse, the synaptic delay and time course of transmitter release become accelerated during the developmental period of hearing acquisition. To address how the distance between voltage-gated Ca2+ channels (VGCCs) and synaptic vesicles (SVs) contribute to this change, we used numerical simulations of a Ca2+ reaction-diffusion model, combined with a SV release model. Our simulations, taking account into single channel current and channel open probability, indicate that the presence of a VGCC cluster in the active zone is essential for reliable, i.e. high efficacy neurotransmission in response to single action potentials. The time course of transmitter release can be reproduced by simulation assuming that SVs are located at several tens of nanometers from the perimeter of VGCC clusters. In this topographical arrangement, shortening the SV-VGCC perimeter coupling distance from 30 to 20 nm reproduced the developmental acceleration of the release time course. Furthermore this SV-VGCC topographical arrangement could reproduce the time course of multiple release components observed at this synapse in response to step depolarizations. We conclude that the SV-VGCC perimeter coupling distance critically determines the time course of SV transmitter release, and propose that the different release time courses can arise from different VGCC-SV perimeter coupling distances.

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