Neuron
Volume 101, Issue 2, 16 January 2019, Pages 260-273.e6
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Article
CaV2.1 α1 Subunit Expression Regulates Presynaptic CaV2.1 Abundance and Synaptic Strength at a Central Synapse

https://doi.org/10.1016/j.neuron.2018.11.028Get rights and content
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Highlights

  • CaV2.1 dominate presynaptic active zones are not fully occupied by CaV2.1 channels

  • Presynaptic CaV2.1 channel numbers can increase regardless of developmental state

  • Higher synaptic vesicle release probability with increased CaV2.1 channel numbers

  • CaV2.1 completely competes away CaV2.2 channels, but not vice versa

Summary

The abundance of presynaptic CaV2 voltage-gated Ca2+ channels (CaV2) at mammalian active zones (AZs) regulates the efficacy of synaptic transmission. It is proposed that presynaptic CaV2 levels are saturated in AZs due to a finite number of slots that set CaV2 subtype abundance and that CaV2.1 cannot compete for CaV2.2 slots. However, at most AZs, CaV2.1 levels are highest and CaV2.2 levels are developmentally reduced. To investigate CaV2.1 saturation states and preference in AZs, we overexpressed the CaV2.1 and CaV2.2 α1 subunits at the calyx of Held at immature and mature developmental stages. We found that AZs prefer CaV2.1 to CaV2.2. Remarkably, CaV2.1 α1 subunit overexpression drove increased CaV2.1 currents and channel numbers and increased synaptic strength at both developmental stages examined. Therefore, we propose that CaV2.1 levels in the AZ are not saturated and that synaptic strength can be modulated by increasing CaV2.1 levels to regulate neuronal circuit output.

Keywords

calcium channels
release probability
active zone
calyx of Held
CaV2.1
synaptic strength
neuronal circuits
synaptic transmission
synaptic plasticity
viral vectors

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