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Open AccessJournal ArticleDOI

Mitophagy inhibits amyloid-β and tau pathology and reverses cognitive deficits in models of Alzheimer’s disease

TLDR
Evidence that mitophagy is impaired in the hippocampus of AD patients, in induced pluripotent stem cell-derived human AD neurons, and in animal AD models is provided, suggesting that impaired removal of defective mitochondria is a pivotal event in AD pathogenesis and thatMitophagy represents a potential therapeutic intervention.
Abstract
Accumulation of damaged mitochondria is a hallmark of aging and age-related neurodegeneration, including Alzheimer's disease (AD). The molecular mechanisms of impaired mitochondrial homeostasis in AD are being investigated. Here we provide evidence that mitophagy is impaired in the hippocampus of AD patients, in induced pluripotent stem cell-derived human AD neurons, and in animal AD models. In both amyloid-β (Aβ) and tau Caenorhabditis elegans models of AD, mitophagy stimulation (through NAD+ supplementation, urolithin A, and actinonin) reverses memory impairment through PINK-1 (PTEN-induced kinase-1)-, PDR-1 (Parkinson's disease-related-1; parkin)-, or DCT-1 (DAF-16/FOXO-controlled germline-tumor affecting-1)-dependent pathways. Mitophagy diminishes insoluble Aβ1-42 and Aβ1-40 and prevents cognitive impairment in an APP/PS1 mouse model through microglial phagocytosis of extracellular Aβ plaques and suppression of neuroinflammation. Mitophagy enhancement abolishes AD-related tau hyperphosphorylation in human neuronal cells and reverses memory impairment in transgenic tau nematodes and mice. Our findings suggest that impaired removal of defective mitochondria is a pivotal event in AD pathogenesis and that mitophagy represents a potential therapeutic intervention.

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Citations
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Journal ArticleDOI

Dietary High-Fat Promotes Cognitive Impairment by Suppressing Mitophagy

TL;DR: In this article , 13-month-old C57BL/6 mice were fed a normal or high-fat diet (HFD) for 6 months, and the results showed that high fatty acid intake hinders mitophagy and upregulates Tau protein phosphorylation.
Posted ContentDOI

Pathway-based integration of multi-omics data reveals lipidomics alterations validated in an Alzheimer’s Disease mouse model and risk loci carriers

TL;DR: In this paper, the authors analyzed genome-wide association studies (GWAS), transcriptomics and proteomics data obtained from several data repositories to obtain differentially expressed (DE) multi-omics elements in mouse models of Alzheimer's disease.
Journal ArticleDOI

Novel Insight into Functions of Transcription Factor EB (TFEB) in Alzheimer’s Disease and Parkinson’s Disease

TL;DR: In this article , the authors systematically summarize the molecular mechanisms and function of TFEB regulation and discuss the roles of the transcription factor EB and autophagy-lysosome pathways in major neurodegenerative diseases including AD and Parkinson's disease.
Journal ArticleDOI

Regulation of aging by balancing mitochondrial function and antioxidant levels

TL;DR: In this article , the authors used C. elegans as a model to evaluate the effects of FBX and to challenge the enigma of the relationship between ATP and lifespan, and they showed that FBX administration could increase ATP levels without overloading the mitochondria while extending the lifespan.
Book ChapterDOI

Pathological Interaction between DNA Repair and Mitochondrial Dysfunction in ALS

TL;DR: Evidence supports either downregulation or impaired recruitment of DNA repair enzymes in both nuclear and mitochondrial genomes and suggests a complex metabolic dysregulation as a critical component in the promotion of the disease.
References
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TL;DR: In this paper, the authors describe methods for the isolation, complementation and mapping of mutants of Caenorhabditis elegans, a small free-living nematode worm.
Journal ArticleDOI

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Journal Article

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Daniel S. Brenner, +1 more
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Journal ArticleDOI

Alzheimer's Disease Is a Synaptic Failure

TL;DR: Mounting evidence suggests that this syndrome begins with subtle alterations of hippocampal synaptic efficacy prior to frank neuronal degeneration, and that the synaptic dysfunction is caused by diffusible oligomeric assemblies of the amyloid β protein.
Journal ArticleDOI

Triple-Transgenic Model of Alzheimer's Disease with Plaques and Tangles: Intracellular Aβ and Synaptic Dysfunction

TL;DR: The recapitulation of salient features of AD in these mice clarifies the relationships between Abeta, synaptic dysfunction, and tangles and provides a valuable model for evaluating potential AD therapeutics as the impact on both lesions can be assessed.
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