1. L-Type Voltage-Gated Ca2+ Channels Regulate Synaptic-Activity-Triggered Recycling Endosome Fusion in Neuronal Dendrites
- Author
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Matthew J. Kennedy, Brian G. Hiester, Emily S. Gibson, Katharine R. Smith, Brooke L. Sinnen, Ashley M. Bourke, and Sarah G. Cook
- Subjects
0301 basic medicine ,Dendritic spine ,Endosome ,AMPA receptor ,Gating ,Biology ,General Biochemistry, Genetics and Molecular Biology ,dendrite ,03 medical and health sciences ,synapse ,recycling endosome ,lcsh:QH301-705.5 ,long-term potentiation ,synaptic plasticity ,Voltage-gated ion channel ,dendritic spine ,Long-term potentiation ,L-type voltage-gated calcium channel ,NMDA receptor ,Cell biology ,030104 developmental biology ,lcsh:Biology (General) ,Synaptic plasticity ,exocytosis - Abstract
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 Ca2+ from distinct sources. NMDA receptor Ca2+ initiates RE fusion with the plasma membrane, while L-type voltage-gated Ca2+ 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.
- Published
- 2017