Mind the Gap: Mitochondria and the Endoplasmic Reticulum in Neurodegenerative Diseases

被引:29
|
作者
Leal, Nuno Santos [1 ]
Martins, Luis Miguel [1 ]
机构
[1] Univ Cambridge, MRC Toxicol Unit, Cambridge CB2 1QR, England
基金
英国医学研究理事会;
关键词
mitochondria-ER contact sites (MERCS); mitochondria-ER associated membrane (MAM); neurodegeneration; neurodegenerative diseases; Alzheimer's disease; Parkinson's disease; amyotrophic lateral sclerosis; frontotemporal dementia; PYRUVATE-DEHYDROGENASE PHOSPHATASE; APOPTOTIC CA2+ SIGNALS; BETA PROTEIN-PRECURSOR; ALZHEIMERS-DISEASE; AMYLOID-BETA; MITOFUSIN; ER MEMBRANES; MOUSE MODEL; PHOSPHOLIPID-SYNTHESIS; CELL BIOENERGETICS;
D O I
10.3390/biomedicines9020227
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The way organelles are viewed by cell biologists is quickly changing. For many years, these cellular entities were thought to be unique and singular structures that performed specific roles. However, in recent decades, researchers have discovered that organelles are dynamic and form physical contacts. In addition, organelle interactions modulate several vital biological functions, and the dysregulation of these contacts is involved in cell dysfunction and different pathologies, including neurodegenerative diseases. Mitochondria-ER contact sites (MERCS) are among the most extensively studied and understood juxtapositioned interorganelle structures. In this review, we summarise the major biological and ultrastructural dysfunctions of MERCS in neurodegeneration, with a particular focus on Alzheimer's disease as well as Parkinson's disease, amyotrophic lateral sclerosis and frontotemporal dementia. We also propose an updated version of the MERCS hypothesis in Alzheimer's disease based on new findings. Finally, we discuss the possibility of MERCS being used as possible drug targets to halt cell death and neurodegeneration.
引用
收藏
页码:1 / 35
页数:35
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