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Autophagy-dependent rhodopsin degradation prevents retinal degeneration in Drosophila.
- Source :
-
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2010 Aug 11; Vol. 30 (32), pp. 10703-19. - Publication Year :
- 2010
-
Abstract
- Recent studies have demonstrated protective roles for autophagy in various neurodegenerative disorders, including the polyglutamine diseases; however, the role of autophagy in retinal degeneration has remained unclear. Accumulation of activated rhodopsin in some Drosophila mutants leads to retinal degeneration, and although it is known that activated rhodopsin is degraded in endosomal pathways in normal photoreceptor cells, the contribution of autophagy to rhodopsin regulation has remained elusive. This study reveals that activated rhodopsin is degraded by autophagy in collaboration with endosomal pathways to prevent retinal degeneration. Light-dependent retinal degeneration in the Drosophila visual system is caused by the knockdown or mutation of autophagy-essential components, such as autophagy-related protein 7 and 8 (atg-7/atg-8), or genes essential for PE (phosphatidylethanolamine) biogenesis and autophagosome formation, including Phosphatidylserine decarboxylase (Psd) and CDP-ethanolamine:diacylglycerol ethanolaminephosphotransferase (Ept). The knockdown of atg-7/8 or Psd/Ept produced an increase in the amount of rhodopsin localized to Rab7-positive late endosomes. This rhodopsin accumulation, followed by retinal degeneration, was suppressed by overexpression of Rab7, which accelerated the endosomal degradation pathway. These results indicate a degree of cross talk between the autophagic and endosomal/lysosomal pathways. Importantly, a reduction in rhodopsin levels rescued Psd knockdown-induced retinal degeneration. Additionally, the Psd knockdown-induced retinal degeneration phenotype was enhanced by Ppt1 inactivation, which causes infantile neuronal ceroid lipofuscinosis, implying that autophagy plays a significant role in its pathogenesis. Collectively, the current data reveal that autophagy suppresses light-dependent retinal degeneration in collaboration with the endosomal degradation pathway and that rhodopsin is a key substrate for autophagic degradation in this context.
- Subjects :
- Animals
Animals, Genetically Modified
Disease Models, Animal
Drosophila
Drosophila Proteins genetics
Drosophila Proteins metabolism
Endosomes metabolism
Endosomes ultrastructure
Gene Expression Regulation genetics
Gene Expression Regulation physiology
Green Fluorescent Proteins genetics
In Situ Nick-End Labeling methods
Larva
Light adverse effects
Lysosomes metabolism
Lysosomes ultrastructure
Membrane Proteins genetics
Membrane Proteins metabolism
Microscopy, Electron, Transmission methods
Microscopy, Immunoelectron methods
Mutation genetics
Nerve Tissue Proteins genetics
Nerve Tissue Proteins metabolism
Photoreceptor Cells, Invertebrate ultrastructure
RNA Interference physiology
Retinal Degeneration etiology
Retinal Degeneration genetics
Rhodopsin genetics
Statistics, Nonparametric
Thiolester Hydrolases
Time Factors
rab GTP-Binding Proteins metabolism
rab7 GTP-Binding Proteins
Autophagy physiology
Photoreceptor Cells, Invertebrate metabolism
Retinal Degeneration prevention & control
Rhodopsin metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2401
- Volume :
- 30
- Issue :
- 32
- Database :
- MEDLINE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 20702701
- Full Text :
- https://doi.org/10.1523/JNEUROSCI.2061-10.2010