Literature DB >> 26987902

Loss of Mitochondrial Function Impairs Lysosomes.

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.
© 2016 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  Parkin; lysosome; mitochondria; neurodegenerative disease; reactive oxygen species (ROS)

Mesh:

Substances:

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


  68 in total

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