A dual role for Ca<sub>v</sub>1.4 Ca<sup>2+</sup> channels in the molecular and structural organization of the rod photoreceptor synapse.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 32940604.
- Also identified by DOI 10.7554/eLife.62184 and PMC identifier 7561352.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Synapses are fundamental information processing units that rely on voltage-gated Ca<sup>2+</sup> (Ca<sub>v</sub>) channels to trigger Ca<sup>2+</sup>-dependent neurotransmitter release. Ca<sub>v</sub> channels also play Ca<sup>2+</sup>-independent roles in other biological contexts, but whether they do so in axon terminals is unknown. Here, we addressed this unknown with respect to the requirement for Ca<sub>v</sub>1.4 L-type channels for the formation of rod photoreceptor synapses in the retina. Using a mouse strain expressing a non-conducting mutant form of Ca<sub>v</sub>1.4, we report that the Ca<sub>v</sub>1.4 protein, but not its Ca<sup>2+</sup> conductance, is required for the molecular assembly of rod synapses; however, Ca<sub>v</sub>1.4 Ca<sup>2+</sup> signals are needed for the appropriate recruitment of postsynaptic partners. Our results support a model in which presynaptic Ca<sub>v</sub> channels serve both as organizers of synaptic building blocks and as sources of Ca<sup>2+</sup> ions in building the first synapse of the visual pathway and perhaps more broadly in the nervous system.
Medical subject headings
- Calcium Channels, L-Type
- Presynaptic Terminals
- Retinal Rod Photoreceptor Cells
- Synapses
- Synaptic Transmission