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Molecular Dysfunctions of Mitochondria-Associated Membranes (MAMs) in Alzheimer's Disease

期刊

出版社

MDPI
DOI: 10.3390/ijms21249521

关键词

endoplasmic reticulum (ER); mitochondria; mitochondria-associated membranes (MAMs); Alzheimer’ s disease (AD); calcium signaling; phospholipids; cholesterol; fatty acid; lipids; unfolded protein response (UPR); APOE; tau; β amyloid precursor protein (APP); amyloid β peptide (Aβ ); APP-C-terminal fragments (APP-CTFs)

资金

  1. LABEX (excellence laboratory, program investment for the future) DISTALZ (Development of Innovative Strategies for a Transdisciplinary approach to Alzheimer's disease)
  2. Fondation Vaincre Alzheimer to MC and by Sao Paulo Research Foundation (FAPESP) [2019/26084-2]

向作者/读者索取更多资源

Alzheimer's disease (AD) is a multifactorial neurodegenerative pathology characterized by a progressive decline of cognitive functions. Alteration of various signaling cascades affecting distinct subcellular compartment functions and their communication likely contribute to AD progression. Among others, the alteration of the physical association between the endoplasmic reticulum (ER) and mitochondria, also referred as mitochondria-associated membranes (MAMs), impacts various cellular housekeeping functions such as phospholipids-, glucose-, cholesterol-, and fatty-acid-metabolism, as well as calcium signaling, which are all altered in AD. Our review describes the physical and functional proteome crosstalk between the ER and mitochondria and highlights the contribution of distinct molecular components of MAMs to mitochondrial and ER dysfunctions in AD progression. We also discuss potential strategies targeting MAMs to improve mitochondria and ER functions in AD.

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