Asynchronous release sites align with NMDA receptors in mouse hippocampal synapses

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作者
Shuo Li
Sumana Raychaudhuri
Stephen Alexander Lee
Marisa M. Brockmann
Jing Wang
Grant Kusick
Christine Prater
Sarah Syed
Hanieh Falahati
Raul Ramos
Tomas M. Bartol
Eric Hosy
Shigeki Watanabe
机构
[1] Johns Hopkins University,Department of Cell Biology
[2] School of Medicine,Department of Biological and Molecular Biology
[3] Johns Hopkins Bloomberg School of Public Health,Neurobiology Course
[4] The Marine Biological Laboratory,Institute of Neurophysiology
[5] Charité Universitätsmedizin,Biochemistry, Cellular and Molecular Biology Graduate Program
[6] ThermoFisher Scientific,Interdisciplinary Institute for Neuroscience
[7] Johns Hopkins University,Solomon H. Snyder Department of Neuroscience
[8] School of Medicine,Department of Biomedical Engineering
[9] Salk Institute for Biological Studies,Department of Pharmacology and Neuroscience, School of Medicine
[10] Centre National de la Recherche Scientifique,Department of Neuroscience
[11] University of Bordeaux,Department of Biology
[12] Johns Hopkins University,undefined
[13] School of Medicine,undefined
[14] Columbia University,undefined
[15] Texas Tech University Health Sciences Center,undefined
[16] Yale University School of Medicine,undefined
[17] Brandeis University,undefined
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摘要
Neurotransmitter is released synchronously and asynchronously following an action potential. Our recent study indicates that the release sites of these two phases are segregated within an active zone, with asynchronous release sites enriched near the center in mouse hippocampal synapses. Here we demonstrate that synchronous and asynchronous release sites are aligned with AMPA receptor and NMDA receptor clusters, respectively. Computational simulations indicate that this spatial and temporal arrangement of release can lead to maximal membrane depolarization through AMPA receptors, alleviating the pore-blocking magnesium leading to greater activation of NMDA receptors. Together, these results suggest that release sites are likely organized to activate NMDA receptors efficiently.
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