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From the Institut National de la Santé et de la Recherche Médicale, Paris, France.
PURPOSE. Proteins of the arrestin family contribute to the regulation of G-proteinmediated transduction. In this study, the presence of ß-arrestins in ocular tissues was investigated.
METHODS. Mouse monoclonal and rabbit polyclonal antibodies were raised against the peptide Val-Asp-Thr-Asn-Ile-Leu-Glu-Leu-Asp-Thr-Asn-Asp-Asp-Asp-Ile, a sequence present in ß-arrestins 1 and 2 but absent from visual arrestin. These antibodies were used for the immunohistologic detection of ß-arrestins in parafin sections of rodent eyes fixed in Bouins solution. Reverse transcriptionpolymerase chain reaction (RT-PCR) analysis of RNA from bovine retina, retinal pigmented epithelial (RPE) cells, lens epithelial cells, and human corneal fibroblasts was performed using ß-1 arrestin primers.
RESULTS. In the eye, ß-arrestin staining predominated in RPE, inner segments of photoreceptors, synaptic spherules of rods, inner plexiform layer and ganglion cell fibers, epithelial cells from ciliary body, and vessels. RT- PCR amplified a 480 bp product, corresponding to the predicted length. The sequence of PCR products from bovine retina and RPE cells was identical with the bovine ß-arrestin mRNA.
CONCLUSIONS. ß-arrestins were detected in several ocular tissues. In photoreceptor cells, their specific localization in the synaptic terminals and plexiform layer suggests a role of ß-arrestin in synaptic transmission. In other ocular tissues, the presence of ß-arrestin may be related either to adrenergic signal transduction or to signal transduction mediated by other G-proteincoupled receptors.
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