Ayten, Monika; Díaz-Lezama, Nundehui; Ghanawi, Hanaa; Haffelder, Felia C.; Kajtna, Jacqueline; Straub, Tobias; Borso, Marco; Imhof, Axel; Hauck, Stefanie M.; Koch, Susanne F. (2024): Metabolic plasticity in a Pde6b retinitis pigmentosa mouse model following rescue. Molecular Metabolism, 88: 101994. ISSN 22128778
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Abstract
Objective
Retinitis pigmentosa (RP) is a hereditary retinal disease characterized by progressive photoreceptor degeneration, leading to vision loss. The best hope for a cure for RP lies in gene therapy. However, given that RP patients are most often diagnosed in the midst of ongoing photoreceptor degeneration, it is unknown how the retinal proteome changes as RP disease progresses, and which changes can be prevented, halted, or reversed by gene therapy.
Methods
Here, we used a Pde6b-deficient RP gene therapy mouse model and performed untargeted proteomic analysis to identify changes in protein expression during degeneration and after treatment.
Results
We demonstrated that Pde6b gene restoration led to a novel form of homeostatic plasticity in rod phototransduction which functionally compensates for the decreased number of rods. By profiling protein levels of metabolic genes and measuring metabolites, we observed an upregulation of proteins associated with oxidative phosphorylation in mutant and treated photoreceptors.
Conclusion
In conclusion, the metabolic demands of the retina differ in our Pde6b-deficient RP mouse model and are not rescued by gene therapy treatment. These findings provide novel insights into features of both RP disease progression and long-term rescue with gene therapy.
Doc-Type: | Article (LMU) |
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Organisational unit (Faculties): | 18 Chemistry and Pharmacy > Department of Pharmacy |
DFG subject classification of scientific disciplines: | Natural sciences |
Date Deposited: | 02. May 2025 09:33 |
Last Modified: | 02. May 2025 11:22 |
URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/1703 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 491502892 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 393313446 |