| Literature DB >> 26987902 |
Julie Demers-Lamarche1, Gérald Guillebaud1, Mouna Tlili2, Kiran Todkar1, Noémie Bélanger2, Martine Grondin2, Angela P Nguyen3, Jennifer Michel2, Marc Germain4.
Abstract
Alterations in mitochondrial function, as observed in neurodegenerative diseases, lead to disrupted energy metabolism and production of damaging reactive oxygen species. Here, we demonstrate that mitochondrial dysfunction also disrupts the structure and function of lysosomes, the main degradation and recycling organelle. Specifically, inhibition of mitochondrial function, following deletion of the mitochondrial protein AIF, OPA1, or PINK1, as well as chemical inhibition of the electron transport chain, impaired lysosomal activity and caused the appearance of large lysosomal vacuoles. Importantly, our results show that lysosomal impairment is dependent on reactive oxygen species. Given that alterations in both mitochondrial function and lysosomal activity are key features of neurodegenerative diseases, this work provides important insights into the etiology of neurodegenerative diseases.Entities:
Keywords: Parkin; lysosome; mitochondria; neurodegenerative disease; reactive oxygen species (ROS)
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Year: 2016 PMID: 26987902 PMCID: PMC4858975 DOI: 10.1074/jbc.M115.695825
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157