Journal
NATURE NEUROSCIENCE
Volume 12, Issue 1, Pages 44-52Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nn.2234
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Funding
- US National Institutes of Health [RO1 EY014466]
- Macular Vision Research Foundation
- Foundation for Retinal Research
- Howard Hughes Medical Institute
- EMBO
- NATIONAL EYE INSTITUTE [R01EY014466] Funding Source: NIH RePORTER
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Retinitis pigmentosa is an incurable retinal disease that leads to blindness. One puzzling aspect concerns the progression of the disease. Although most mutations that cause retinitis pigmentosa are in rod photoreceptor - specific genes, cone photoreceptors also die as a result of such mutations. To understand the mechanism of non-autonomous cone death, we analyzed four mouse models harboring mutations in rod- specific genes. We found changes in the insulin/mammalian target of rapamycin pathway that coincided with the activation of autophagy during the period of cone death. We increased or decreased the insulin level and measured the survival of cones in one of the models. Mice that were treated systemically with insulin had prolonged cone survival, whereas depletion of endogenous insulin had the opposite effect. These data suggest that the non- autonomous cone death in retinitis pigmentosa could, at least in part, be a result of the starvation of cones.
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