Role of mtDNA disturbances in the pathogenesis of Alzheimer’s and Parkinson’s disease

[Display omitted] •mtDNA disturbances are associated with AD and PD pathogenesis.•Mitochondrial oxidative stress is one of main pathological mechanisms.•Disturbs of oxidative phosphorylation generate most ROS in the neurons.•ROS level correlates with neuroinflammation and aggregation of Aβ, α-syn an...

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Veröffentlicht in:DNA repair 2020-07, Vol.91-92, p.102871-102871, Article 102871
Hauptverfasser: Antonyová, Veronika, Kejík, Zdeněk, Brogyányi, Tereza, Kaplánek, Robert, Pajková, Martina, Talianová, Veronika, Hromádka, Róbert, Masařík, Michal, Sýkora, David, Mikšátková, Lucie, Martásek, Pavel, Jakubek, Milan
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Sprache:eng
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Zusammenfassung:[Display omitted] •mtDNA disturbances are associated with AD and PD pathogenesis.•Mitochondrial oxidative stress is one of main pathological mechanisms.•Disturbs of oxidative phosphorylation generate most ROS in the neurons.•ROS level correlates with neuroinflammation and aggregation of Aβ, α-syn and tau.•mtDNA haplogroups can be used to predict AD and PD risk and development. Neurodegenerative diseases (e.g. Alzheimer’s and Parkinson’s disease) are becoming increasingly problematic to healthcare systems. Therefore, their underlying mechanisms are trending topics of study in medicinal research. Numerous studies have evidenced a strong association between mitochondrial DNA disturbances (e.g. oxidative damage, mutations, and methylation shifts) and the initiation and progression of neurodegenerative diseases. Therefore, this review discusses the risk and development of neurodegenerative diseases in terms of disturbances in mitochondrial DNA and as a part of a complex ecosystem that includes other important mechanisms (e.g. neuroinflammation and the misfolding and aggregation of amyloid-β peptides, α-synuclein, and tau proteins). In addition, the influence of individual mitochondrial DNA haplogroups on the risk and development of neurodegenerative diseases is also described and discussed.
ISSN:1568-7864
1568-7856
DOI:10.1016/j.dnarep.2020.102871