Activation of mitochondrial TRAP1 stimulates mitochondria-lysosome crosstalk and correction of lysosomal dysfunction Journal Article


Authors: Chen, F. W.; Davies, J. P.; Calvo, R.; Chaudhari, J.; Dolios, G.; Taylor, M. K.; Patnaik, S.; Dehdashti, J.; Mull, R.; Dranchack, P.; Wang, A.; Xu, X.; Hughes, E.; Southall, N.; Ferrer, M.; Wang, R.; Marugan, J. J.; Ioannou, Y. A.
Article Title: Activation of mitochondrial TRAP1 stimulates mitochondria-lysosome crosstalk and correction of lysosomal dysfunction
Abstract: Numerous studies have established the involvement of lysosomal and mitochondrial dysfunction in the pathogenesis of neurodegenerative disorders such as Alzheimer's and Parkinson diseases. Building on our previous studies of the neurodegenerative lysosomal lipidosis Niemann–Pick C1 (NPC1), we have unexpectedly discovered that activation of the mitochondrial chaperone tumor necrosis factor receptor-associated protein 1 (TRAP1) leads to the correction of the lysosomal storage phenotype in patient cells from multiple lysosomal storage disorders including NPC1. Using small compound activators specific for TRAP1, we find that activation of this chaperone leads to a generalized restoration of lysosomal and mitochondrial health. Mechanistically, we show that this process includes inhibition of oxidative phosphorylation and reduction of oxidative stress, which results in activation of AMPK and ultimately stimulates lysosome recycling. Thus, TRAP1 participates in lysosomal-mitochondrial crosstalk to maintain cellular homeostasis and could represent a potential therapeutic target for multiple disorders. © 2022 The Authors
Keywords: neuroscience; cell biology; cellular neuroscience
Journal Title: iScience
Volume: 25
Issue: 9
ISSN: 2589-0042
Publisher: Cell Press  
Date Published: 2022-09-16
Start Page: 104941
Language: English
DOI: 10.1016/j.isci.2022.104941
PROVIDER: scopus
PMCID: PMC9440283
PUBMED: 36065186
DOI/URL:
Notes: Article -- Export Date: 3 October 2022 -- Source: Scopus
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