Publication date: 5 June 2018
Source:Cell Reports, Volume 23, Issue 10
Author(s): Na-Ryum Bin, Ke Ma, Hidekiyo Harada, Chi-Wei Tien, Fiona Bergin, Kyoko Sugita, Thomas T. Luyben, Masahiro Narimatsu, Zhengping Jia, Jeffrey L. Wrana, Philippe P. Monnier, Liang Zhang, Kenichi Okamoto, Shuzo Sugita
Trafficking of neurotransmitter receptors on postsynaptic membranes is critical for basal neurotransmission and synaptic plasticity, yet the underlying mechanisms remain elusive. Here, we investigated the role of syntaxin 4 in postsynaptic hippocampal CA1 neurons by analyzing conditional knockout (syntaxin 4 cKO) mice. We show that syntaxin 4 cKO resulted in reduction of basal neurotransmission without changes in paired-pulse ratios. Both α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-d-aspartic acid (NMDA) receptor-mediated charge transfers were diminished. Patch-clamp experiments revealed that amplitudes, but not frequencies, of spontaneous excitatory postsynaptic currents are reduced. Syntaxin 4 knockout (KO) caused drastic reduction in expression of surface α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) and N-methyl-d-aspartic acid (NMDA) receptors in cultured hippocampal neurons. Furthermore, cKO caused defects in theta-burst stimulation induced long-term potentiation and spatial learning as assessed by a water maze task, indicating that synaptic plasticity was altered. Our data reveal a crucial role of syntaxin 4 in trafficking of ionotropic glutamate receptors that are essential for basal neurotransmission, synaptic plasticity, and spatial memory.
Graphical abstract
Teaser
Bin et al. find that syntaxin 4 plays an important role in trafficking of AMPA and NMDA receptors in postsynaptic CA1 neurons of the hippocampus. Syntaxin 4 is crucial for mediating basal and synaptic plasticity, which are essential for hippocampus-dependent spatial learning and memory.https://ift.tt/2sEUZ58
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