Human molecular genetics, 2017-02, Vol.26 (4), p.674-685
2017
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- Autor(en) / Beteiligte
- Titel
- Mitochondrial morphology and cellular distribution are altered in SPG31 patients and are linked to DRP1 hyperphosphorylation
- Ist Teil von
- Human molecular genetics, 2017-02, Vol.26 (4), p.674-685
- Ort / Verlag
- England: Oxford University Press (OUP)
- Erscheinungsjahr
- 2017
- Quelle
- Oxford Journals 2020 Medicine
- Beschreibungen/Notizen
- Hereditary spastic paraplegia, SPG31, is a rare neurological disorder caused by mutations in REEP1 gene encoding the microtubule-interacting protein, REEP1. The mechanism by which REEP1-dependent processes are linked with the disease is unclear. REEP1 regulates the morphology and trafficking of various organelles via interaction with the microtubules. In this study, we collected primary fibroblasts from SPG31 patients to investigate their mitochondrial morphology. We observed that the mitochondrial morphology in patient cells was highly tubular compared with control cells. We provide evidence that these morphological alterations are caused by the inhibition of mitochondrial fission protein, DRP1, due to the hyperphosphorylation of its serine 637 residue. This hyperphosphorylation is caused by impaired interactions between REEP1 and mitochondrial phosphatase PGAM5. Genetically or pharmacologically induced decrease of DRP1-S637 phosphorylation restores mitochondrial morphology in patient cells. Furthermore, ectopic expression of REEP1 carrying pathological mutations in primary neuronal culture targets REEP1 to the mitochondria. Mutated REEP1 proteins sequester mitochondria to the perinuclear region of the neurons and therefore, hamper mitochondrial transport along the axon. Considering the established role of mitochondrial distribution and morphology in neuronal health, our results support the involvement of a mitochondrial dysfunction in SPG31 pathology.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0964-6906eISSN: 1460-2083DOI: 10.1093/hmg/ddw425Titel-ID: cdi_hal_primary_oai_HAL_hal_02353858v1
- Format
- –
- Schlagworte
- Animals, Cell Nucleus - genetics, Cell Nucleus - metabolism, Cell Nucleus - pathology, Cells, Cultured, Cellular Biology, Female, GTP Phosphohydrolases - genetics, GTP Phosphohydrolases - metabolism, Humans, Life Sciences, Male, Membrane Transport Proteins - genetics, Membrane Transport Proteins - metabolism, Mice, Microtubule-Associated Proteins - genetics, Microtubule-Associated Proteins - metabolism, Mitochondria - metabolism, Mitochondria - pathology, Mitochondrial Proteins - genetics, Mitochondrial Proteins - metabolism, Neurons - metabolism, Neurons - pathology, Phosphoprotein Phosphatases - genetics, Phosphoprotein Phosphatases - metabolism, Phosphorylation - genetics, Spastic Paraplegia, Hereditary - metabolism, Spastic Paraplegia, Hereditary - pathology