L-Type Voltage-Gated Ca2+ Channels Regulate Synaptic Activity-Triggered Recycling Endosome Fusion in Neuronal Dendrites
Author(s) -
Brian G. Hiester,
Ashley M. Bourke,
Brooke L. Sinnen,
Sarah G. Cook,
Emily S. Gibson,
Katharine R. Smith,
Matthew J. Kennedy
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.10.105
Subject(s) - ampa receptor , microbiology and biotechnology , synaptic plasticity , endosome , nmda receptor , glutamate receptor , chemistry , gating , neuroscience , receptor , biophysics , biology , biochemistry
The repertoire and abundance of proteins displayed on the surface of neuronal dendrites are tuned by regulated fusion of recycling endosomes (REs) with the dendritic plasma membrane. While this process is critical for neuronal function and plasticity, how synaptic activity drives RE fusion remains unexplored. We demonstrate a multistep fusion mechanism that requires Ca 2+ from distinct sources. NMDA receptor Ca 2+ initiates RE fusion with the plasma membrane, while L-type voltage-gated Ca 2+ channels (L-VGCCs) regulate whether fused REs collapse into the membrane or reform without transferring their cargo to the cell surface. Accordingly, NMDA receptor activation triggered AMPA-type glutamate receptor trafficking to the dendritic surface in an L-VGCC-dependent manner. Conversely, potentiating L-VGCCs enhanced AMPA receptor surface expression only when NMDA receptors were also active. Thus L-VGCCs play a role in tuning activity-triggered surface expression of key synaptic proteins by gating the mode of RE fusion.
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