The Journal of Cell Biology · 2008 · 4K citations · 26 references
Life SciencesCell BiologyNeuroscienceAutophagyMitochondrial BiologyMolecular NeuroscienceAutophagy In DiseaseAutophagy RegulationMitochondrial DysfunctionMitochondrial PhysiologyMitophagyParkinson DiseaseDrosophila Disease ModelsDrosophila ModelsEliminationMitophagy SignalingMuscle Fiber DegenerationParkin MutationsParkinson Disease AutophagySkeletal Muscle Degeneration
Loss-of-function mutations in Park2, the gene coding for the ubiquitin ligase Parkin, are a significant cause of early onset Parkinson's disease. Although the role of Parkin in neuron maintenance is unknown, recent work has linked Parkin to the regulation of mitochondria. Its loss is associated with swollen mitochondria and muscle degeneration in Drosophila melanogaster, as well as mitochondrial dysfunction and increased susceptibility to mitochondrial toxins in other species. Here, we show that Parkin is selectively recruited to dysfunctional mitochondria with low membrane potential in mammalian cells. After recruitment, Parkin mediates the engulfment of mitochondria by autophagosomes and the selective elimination of impaired mitochondria. These results show that Parkin promotes autophagy of damaged mitochondria and implicate a failure to eliminate dysfunctional mitochondria in the pathogenesis of Parkinson's disease.
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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Tohru Kitada, Shuichi Asakawa, Nobutaka Hattori et al. · Nature · 1998 · 5.2K citations
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
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Fission and selective fusion govern mitochondrial segregation and elimination by autophagy
Gilad Twig, Álvaro A. Elorza, Anthony Molina et al. · The EMBO Journal · 2008 · 3.1K citations · Full text
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