Literature DB >> 35665766

Mitophagy in Alzheimer's disease: Molecular defects and therapeutic approaches.

Arnaud Mary1, Fanny Eysert1, Frédéric Checler1, Mounia Chami2.   

Abstract

Mitochondrial dysfunctions are central players in Alzheimer's disease (AD). In addition, impairments in mitophagy, the process of selective mitochondrial degradation by autophagy leading to a gradual accumulation of defective mitochondria, have also been reported to occur in AD. We provide an updated overview of the recent discoveries and advancements on mitophagic molecular dysfunctions in AD-derived fluids and cells as well as in AD brains. We discuss studies using AD cellular and animal models that have unraveled the contribution of relevant AD-related proteins (Tau, Aβ, APP-derived fragments and APOE) in mitophagy failure. In accordance with the important role of impaired mitophagy in AD, we report on various therapeutic strategies aiming at stimulating mitophagy in AD and we summarize the benefits of these potential therapeutic strategies in human clinical trials.
© 2022. The Author(s).

Entities:  

Year:  2022        PMID: 35665766     DOI: 10.1038/s41380-022-01631-6

Source DB:  PubMed          Journal:  Mol Psychiatry        ISSN: 1359-4184            Impact factor:   15.992


  73 in total

1.  PARK2 enhancement is able to compensate mitophagy alterations found in sporadic Alzheimer's disease.

Authors:  Patricia Martín-Maestro; Ricardo Gargini; George Perry; Jesús Avila; Vega García-Escudero
Journal:  Hum Mol Genet       Date:  2015-12-31       Impact factor: 6.150

Review 2.  The Cellular Phase of Alzheimer's Disease.

Authors:  Bart De Strooper; Eric Karran
Journal:  Cell       Date:  2016-02-11       Impact factor: 41.582

Review 3.  Mitophagy and Alzheimer's Disease: Cellular and Molecular Mechanisms.

Authors:  Jesse S Kerr; Bryan A Adriaanse; Nigel H Greig; Mark P Mattson; M Zameel Cader; Vilhelm A Bohr; Evandro F Fang
Journal:  Trends Neurosci       Date:  2017-02-09       Impact factor: 13.837

4.  Releasing Syntaphilin Removes Stressed Mitochondria from Axons Independent of Mitophagy under Pathophysiological Conditions.

Authors:  Mei-Yao Lin; Xiu-Tang Cheng; Prasad Tammineni; Yuxiang Xie; Bing Zhou; Qian Cai; Zu-Hang Sheng
Journal:  Neuron       Date:  2017-05-03       Impact factor: 17.173

5.  Reduced Mitochondrial Activity is Early and Steady in the Entorhinal Cortex but it is Mainly Unmodified in the Frontal Cortex in Alzheimer's Disease.

Authors:  Mercedes Armand-Ugon; Belen Ansoleaga; Sara Berjaoui; Isidro Ferrer
Journal:  Curr Alzheimer Res       Date:  2017       Impact factor: 3.498

Review 6.  Re-emphasizing early Alzheimer's disease pathology starting in select entorhinal neurons, with a special focus on mitophagy.

Authors:  Asgeir Kobro-Flatmoen; Maria Jose Lagartos-Donate; Yahyah Aman; Paul Edison; Menno P Witter; Evandro F Fang
Journal:  Ageing Res Rev       Date:  2021-02-20       Impact factor: 10.895

Review 7.  Alzheimer's disease.

Authors:  Colin L Masters; Randall Bateman; Kaj Blennow; Christopher C Rowe; Reisa A Sperling; Jeffrey L Cummings
Journal:  Nat Rev Dis Primers       Date:  2015-10-15       Impact factor: 52.329

Review 8.  The multifaceted nature of amyloid precursor protein and its proteolytic fragments: friends and foes.

Authors:  Hoang S Nhan; Karen Chiang; Edward H Koo
Journal:  Acta Neuropathol       Date:  2014-10-07       Impact factor: 17.088

9.  Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin.

Authors:  Ghazaleh Ashrafi; Julia S Schlehe; Matthew J LaVoie; Thomas L Schwarz
Journal:  J Cell Biol       Date:  2014-08-25       Impact factor: 10.539

10.  Tau accumulation impairs mitophagy via increasing mitochondrial membrane potential and reducing mitochondrial Parkin.

Authors:  Yu Hu; Xia-Chun Li; Zhi-hao Wang; Yu Luo; Xiangnan Zhang; Xiu-Ping Liu; Qiong Feng; Qun Wang; Zhenyu Yue; Zhong Chen; Keqiang Ye; Jian-Zhi Wang; Gong-Ping Liu
Journal:  Oncotarget       Date:  2016-04-05
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