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Publication : Photoreceptor-like cells in transgenic mouse eye.

First Author  Yan RT Year  2013
Journal  Invest Ophthalmol Vis Sci Volume  54
Issue  7 Pages  4766-75
PubMed ID  23847312 Mgi Jnum  J:214177
Mgi Id  MGI:5588529 Doi  10.1167/iovs.13-11936
Citation  Yan RT, et al. (2013) Photoreceptor-like cells in transgenic mouse eye. Invest Ophthalmol Vis Sci 54(7):4766-75
abstractText  PURPOSE: Recent success of rescuing vision by photoreceptor replacement in mouse models of photoreceptor degeneration intensifies the need to identify approaches to generate photoreceptors cells for future replacement therapies. We explored the possibility of whether in the mouse eye photoreceptor-like cells could arise from the RPE experimentally manipulated to express a regulatory gene participating in transcriptional networks leading to photoreceptor genesis during retinal development. METHODS: Transgenic mice were generated with a DNA construct that would express neurogenin1 from RPE bestrophin-1 promoter or neurogenin3 from RPE65 promoter. Transgenic mice were examined with histology and immunohistology for the presence of photoreceptor-like cells and for the presence of cells that might represent transitional stages in RPE-to-photoreceptor reprogramming. Explant culture of "sclera+choroid+RPE" eyecup was used to examine whether cells with photoreceptor traits could arise from the eyecup derived from transgenic mice. RESULTS: Transgenic animals showed varied degrees of phenotype manifestation. Approximately 60% of offspring from approximately 50% of founders contained photoreceptor-like cells in the subretinal space. These cells expressed photoreceptor proteins recoverin, red opsin, and rhodopsin, and displayed morphologic similarities to photoreceptors. In these eyes, the RPE was maintained. Cells seemingly amid RPE-to-photoreceptor transformation were observed in young and aged mice, suggesting old animals were responsive to the reprogramming scheme. De novo generation of photoreceptor-like cells was detected in "sclera+choroid+RPE" eyecup explants derived from adult animals. CONCLUSIONS: Our results point to a potential way to generate photoreceptor cells in situ in adult mammalian eyes.
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