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http://purl.uniprot.org/citations/31335952http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31335952http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

Cav1.4 is a voltage-gated calcium channel clustered at the presynaptic active zones of photoreceptors. Cav1.4 functions in communication by mediating the Ca2+ influx that triggers neurotransmitter release. It also aids in development since rod ribbon synapses do not form in Cav1.4 knock-out mice. Here we used a rescue strategy to investigate the ability of Cav1.4 to trigger synaptogenesis in both immature and mature mouse rods.

Methods

In vivo electroporation was used to transiently express Cav α1F or tamoxifen-inducible Cav α1F in a subset of Cav1.4 knock-out mouse rods. Synaptogenesis was assayed using morphologic markers and a vision-guided water maze.

Results

We found that introduction of Cav α1F to knock-out terminals rescued synaptic development as indicated by PSD-95 expression and elongated ribbons. When expression of Cav α1F was induced in mature animals, we again found restoration of PSD-95 and elongated ribbons. However, the induced expression of Cav α1F led to diffuse distribution of Cav α1F in the terminal instead of being clustered beneath the ribbon. Approximately a quarter of treated animals passed the water maze test, suggesting the rescue of retinal signaling in these mice.

Conclusions

These data confirm that Cav α1F expression is necessary for rod synaptic terminal development and demonstrate that rescue is robust even in adult animals with late stages of synaptic disease. The degree of rod synaptic plasticity seen here should be sufficient to support future vision-restoring treatments such as gene or cell replacement that will require photoreceptor synaptic rewiring."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.org/dc/terms/identifier"doi:10.1167/iovs.19-27226"xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/author"Lee A."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/author"Baker S.A."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/author"Kerov V."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/author"Laird J.G."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/author"Gardner S.H."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/author"Kopel A.J."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/name"Invest Ophthalmol Vis Sci"xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/pages"3150-3161"xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/title"Rescue of Rod Synapses by Induction of Cav Alpha 1F in the Mature Cav1.4 Knock-Out Mouse Retina."xsd:string
http://purl.uniprot.org/citations/31335952http://purl.uniprot.org/core/volume"60"xsd:string
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