| Literature DB >> 25631988 |
Luis Pérez de Sevilla Müller1, Allison Sargoy1,2,3, Laura Fernández-Sánchez4, Allen Rodriguez1, Janelle Liu1, Nicolás Cuenca4, Nicholas Brecha1,2,3,5,6.
Abstract
High-voltage-activated calcium channels are hetero-oligomeric protein complexes that mediate multiple cellular processes, including the influx of extracellular Ca(2+), neurotransmitter release, gene transcription, and synaptic plasticity. These channels consist of a primary α(1) pore-forming subunit, which is associated with an extracellular α(2)δ subunit and an intracellular β auxiliary subunit, which alter the gating properties and trafficking of the calcium channel. The cellular localization of the α(2)δ(3) subunit in the mouse and rat retina is unknown. In this study using RT-PCR, a single band at ∼ 305 bp corresponding to the predicted size of the α(2)δ(3) subunit fragment was found in mouse and rat retina and brain homogenates. Western blotting of rodent retina and brain homogenates showed a single 123-kDa band. Immunohistochemistry with an affinity-purified antibody to the α(2)δ(3) subunit revealed immunoreactive cell bodies in the ganglion cell layer and inner nuclear layer and immunoreactive processes in the inner plexiform layer and the outer plexiform layer. α(2)δ(3) immunoreactivity was localized to multiple cell types, including ganglion, amacrine, and bipolar cells and photoreceptors, but not horizontal cells. The expression of the α(2)δ(3) calcium channel subunit to multiple cell types suggests that this subunit participates widely in Ca-channel-mediated signaling in the retina.Entities:
Keywords: amacrine cell; calcium channel; ganglion cell; photoreceptor; retina; α2δ3 subunit
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Year: 2015 PMID: 25631988 PMCID: PMC4439319 DOI: 10.1002/cne.23751
Source DB: PubMed Journal: J Comp Neurol ISSN: 0021-9967 Impact factor: 3.215