Deciphering the role of PGC-1α in neurological disorders: from mitochondrial dysfunction to synaptic failure

被引:48
作者
Panes, Jessica D. [1 ]
Wendt, Aline [1 ]
Ramirez-Molina, Oscar [1 ]
Castro, Patricio A. [3 ]
Fuentealba, Jorge [1 ,2 ]
机构
[1] Univ Concepcion, Fac Ciencias Biol, Dept Fisiol, Lab Screening Compuestos Neuroact LSCN, Concepcion, Chile
[2] Univ Concepcion, Fac Ciencias Biol, Ctr Invest Avanzadas Biomed CIAB UdeC, Concepcion, Chile
[3] Univ Concepcion, Fac Ciencias Biol, Dept Fisiol, Concepcion, Chile
关键词
ALZHEIMERS-DISEASE; HUNTINGTONS-DISEASE; TRANSCRIPTIONAL REPRESSION; COGNITIVE IMPAIRMENT; SOLUBLE OLIGOMERS; VASCULAR DEMENTIA; MOUSE MODEL; PPAR-GAMMA; COACTIVATOR; BIOGENESIS;
D O I
10.4103/1673-5374.317957
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The onset and mechanisms underlying neurodegenerative diseases remain uncertain. The main features of neurodegenerative diseases have been related with cellular and molecular events like neuronal loss, mitochondrial dysfunction and aberrant accumulation of misfolded proteins or peptides in specific areas of the brain. The most prevalent neurodegenerative diseases belonging to age-related pathologies are Alzheimer's disease, Huntington's disease, Parkinson's disease and amyotrophic lateral sclerosis. Interestingly, mitochondrial dysfunction has been observed to occur during the early onset of several neuropathological events associated to neurodegenerative diseases. The master regulator of mitochondrial quality control and energetic metabolism is the transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1 alpha). Additionally, it has been observed that PGC-1 alpha appears to be a key factor in maintaining neuronal survival and synaptic transmission. In fact, PGC-1 alpha downregulation in different brain areas (hippocampus, substantia nigra, cortex, striatum and spinal cord) that occurs in function of neurological damage including oxidative stress, neuronal loss, and motor disorders has been seen in several animal and cellular models of neurodegenerative diseases. Current evidence indicates that PGC-1 alpha upregulation may serve as a potent therapeutic approach against development and progression of neuronal damage. Remarkably, increasing evidence shows that PGC-1 alpha deficient mice have neurodegenerative diseases-like features, as well as neurological abnormalities. Finally, we discuss recent studies showing novel specific PGC-1 alpha isoforms in the central nervous system that appear to exert a key role in the age of onset of neurodegenerative diseases and have a neuroprotective function in the central nervous system, thus opening a new molecular strategy for treatment of neurodegenerative diseases. The purpose of this review is to provide an up-to-date overview of the PGC-1 alpha role in the physiopathology of neurodegenerative diseases, as well as establish the importance of PGC-1 alpha function in synaptic transmission and neuronal survival.
引用
收藏
页码:237 / +
页数:11
相关论文
共 128 条
[1]   Deposition of 5-Methylcytosine on Enhancer RNAs Enables the Coactivator Function of PGC-1α [J].
Aguilo, Francesca ;
Li, SiDe ;
Balasubramaniyan, Natarajan ;
Sancho, Ana ;
Benko, Sabina ;
Zhang, Fan ;
Vashisht, Ajay ;
Rengasamy, Madhumitha ;
Andino, Blanca ;
Chen, Chih-hung ;
Zhou, Felix ;
Qian, Chengmin ;
Zhou, Ming-Ming ;
Wohlschlegel, James A. ;
Zhang, Weijia ;
Suchy, Frederick J. ;
Walsh, Martin J. .
CELL REPORTS, 2016, 14 (03) :479-492
[2]   Dynamic regulation of PGC-1α localization and turnover implicates mitochondrial adaptation in calorie restriction and the stress response [J].
Anderson, Rozalyn M. ;
Barger, Jamie L. ;
Edwards, Michael G. ;
Braun, Kristina H. ;
O'Connor, Clare E. ;
Prolla, Tomas A. ;
Weindruch, Richard .
AGING CELL, 2008, 7 (01) :101-111
[3]   Exploring the Role of P2X Receptors in Alzheimer's Disease [J].
Andrea Godoy, Pamela ;
Ramirez-Molina, Oscar ;
Fuentealba, Jorge .
FRONTIERS IN PHARMACOLOGY, 2019, 10
[4]   Morphological and functional remodelling of the neuromuscular junction by skeletal muscle PGC-1α [J].
Arnold, Anne-Sophie ;
Gill, Jonathan ;
Christe, Martine ;
Ruiz, Rocio ;
McGuirk, Shawn ;
St-Pierre, Julie ;
Tabares, Lucia ;
Handschin, Christoph .
NATURE COMMUNICATIONS, 2014, 5
[5]   Nucleus or cytoplasm? The mysterious case of SIRT1's subcellular localization [J].
Bai, Wenlong ;
Zhang, Xiaohong .
CELL CYCLE, 2016, 15 (24) :3337-3338
[6]   Alzheimer's disease [J].
Ballard, Clive ;
Gauthier, Serge ;
Corbett, Anne ;
Brayne, Carol ;
Aarsland, Dag ;
Jones, Emma .
LANCET, 2011, 377 (9770) :1019-1031
[7]   Interneuron Transcriptional Dysregulation Causes Frequency-Dependent Alterations in the Balance of Inhibition and Excitation in Hippocampus [J].
Bartley, Aundrea F. ;
Lucas, Elizabeth K. ;
Brady, Lillian J. ;
Li, Qin ;
Hablitz, John J. ;
Cowell, Rita M. ;
Dobrunz, Lynn E. .
JOURNAL OF NEUROSCIENCE, 2015, 35 (46) :15276-15290
[8]  
Baskys A, 2007, CLIN INTERV AGING, V2, P327
[9]   ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues [J].
Bayer, Hanna ;
Lang, Kerstin ;
Buck, Eva ;
Higelin, Julia ;
Barteczko, Lara ;
Pasquarelli, Noemi ;
Sprissler, Jasmin ;
Lucas, Tanja ;
Holzmann, Karlheinz ;
Demestre, Maria ;
Lindenberg, Katrin S. ;
Danzer, Karin M. ;
Boeckers, Tobias ;
Ludolph, Albert C. ;
Dupuis, Luc ;
Weydt, Patrick ;
Witting, Anke .
NEUROBIOLOGY OF DISEASE, 2017, 97 :36-45
[10]   The selective anatomical vulnerability of ALS: 'disease-defining' and 'disease-defying' brain regions [J].
Bede, Peter ;
Iyer, Parameswaran M. ;
Schuster, Christina ;
Elamin, Marwa ;
Mclaughlin, Russell L. ;
Kenna, Kevin ;
Hardiman, Orla .
AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION, 2016, 17 (7-8) :561-570