Abstract
A prime goal of regenerative medicine is to direct cell fates in a therapeutically useful manner. Retinitis pigmentosa is one of the most common degenerative diseases of the eye and is associated with early rod photoreceptor death followed by secondary cone degeneration. We hypothesized that converting adult rods into cones, via knockdown of the rod photoreceptor determinant Nrl, could make the cells resistant to the effects of mutations in rod-specific genes, thereby preventing secondary cone loss. To test this idea, we engineered a tamoxifen-inducible allele of Nrl to acutely inactivate the gene in adult rods. This manipulation resulted in reprogramming of rods into cells with a variety of cone-like molecular, histologic, and functional properties. Moreover, reprogramming of adult rods achieved cellular and functional rescue of retinal degeneration in a mouse model of retinitis pigmentosa. These findings suggest that elimination of Nrl in adult rods may represent a unique therapy for retinal degeneration.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Basic-Leucine Zipper Transcription Factors / deficiency
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Basic-Leucine Zipper Transcription Factors / genetics*
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CpG Islands / genetics
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DNA Methylation
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Electroretinography
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Eye Proteins / genetics*
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Gene Expression
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Immunohistochemistry
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In Situ Hybridization
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Mice
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Mice, Inbred C57BL
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Mice, Knockout
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Microscopy, Electron
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Retina / metabolism
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Retina / pathology
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Retinal Cone Photoreceptor Cells / metabolism*
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Retinal Cone Photoreceptor Cells / ultrastructure
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Retinal Degeneration / genetics*
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Retinal Degeneration / metabolism
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Retinal Degeneration / physiopathology
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Retinal Rod Photoreceptor Cells / metabolism*
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Retinal Rod Photoreceptor Cells / ultrastructure
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Retinitis Pigmentosa / genetics
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Retinitis Pigmentosa / metabolism
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Retinitis Pigmentosa / physiopathology
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Reverse Transcriptase Polymerase Chain Reaction
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Rhodopsin / deficiency
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Rhodopsin / genetics
Substances
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Basic-Leucine Zipper Transcription Factors
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Eye Proteins
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Nrl protein, mouse
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Rhodopsin