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• W2916632364 endingPage "881" @default.
• W2916632364 startingPage "861" @default.
• W2916632364 abstract "Mitochondrial diseases are a group of rare heterogeneous genetic disorders caused by total or partial mitochondrial dysfunction. They can be caused by mutations in nuclear or mitochondrial DNA (mtDNA). MERRF (Myoclonic Epilepsy with Ragged-Red Fibers) syndrome is one of the most common mitochondrial disorders caused by point mutations in mtDNA. It is mainly caused by the m.8344A > G mutation in the tRNALys (UUR) gene of mtDNA (MT-TK gene). This mutation affects the translation of mtDNA encoded proteins; therefore, the assembly of the electron transport chain (ETC) complexes is disrupted, leading to a reduced mitochondrial respiratory function. However, the molecular pathogenesis of MERRF syndrome remains poorly understood due to the lack of appropriate cell models, particularly in those cell types most affected in the disease such as neurons. Patient-specific induced neurons (iNs) are originated from dermal fibroblasts derived from different individuals carrying the particular mutation causing the disease. Therefore, patient-specific iNs can be used as an excellent cell model to elucidate the mechanisms underlying MERRF syndrome. Here we present for the first time the generation of iNs from MERRF dermal fibroblasts by direct reprograming, as well as a series of pathophysiological characterizations which can be used for testing the impact of a specific mtDNA mutation on neurons and screening for drugs that can correct the phenotype." @default.
• W2916632364 created "2019-03-02" @default.
• W2916632364 creator A5005530192 @default.
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• W2916632364 creator A5048016361 @default.
• W2916632364 creator A5070009149 @default.
• W2916632364 date "2019-05-01" @default.
• W2916632364 modified "2023-10-15" @default.
• W2916632364 title "Pathophysiological characterization of MERRF patient-specific induced neurons generated by direct reprogramming" @default.
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