Ageing and inflammation - A central role for mitochondria in brain health and disease

被引:74
作者
Currais, Antonio [1 ]
机构
[1] Salk Inst Biol Studies, 10010 N Torrey Pines Rd, La Jolla, CA 92037 USA
关键词
Differentiation; Inflammation; Metabolism; Neurodegenerative diseases; PENTOSE-PHOSPHATE PATHWAY; H+-ATP SYNTHASE; CEREBROSPINAL-FLUID LACTATE; CELL-CYCLE PROGRESSION; NF-KAPPA-B; NITRIC-OXIDE; INSULIN-RESISTANCE; AEROBIC GLYCOLYSIS; INNATE IMMUNITY; OXIDATIVE-PHOSPHORYLATION;
D O I
10.1016/j.arr.2015.02.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To develop successful therapies that prevent or treat neurodegenerative diseases requires an understanding of the upstream events. Ageing is by far the greatest risk factor for most of these diseases, and to clarify their causes will require an understanding of the process of ageing itself. Starting with the question Why do we age as individual organisms, but the line of pluripotent embryonic stem cells and germ cells carried by individuals and transmitted to descendants is immortal? this review discusses how the process of cellular differentiation leads to the accumulation of biological imperfections with ageing, and how these imperfections may be the cause of chronic inflammatory responses to stress that undermine cellular function. Both differentiation and inflammation involve drastic metabolic changes associated with alterations in mitochondrial dynamics that shift the balance between aerobic glycolysis and oxidative phosphorylation. With ageing, mitochondrial dysfunction can be both the cause and consequence of inflammatory processes and elicit metabolic adaptations that might be either protective or become progressively detrimental. It is argued here that an understanding of the relationship between metabolism, differentiation and inflammation is essential to understand the pathological mechanisms governing brain health and disease during ageing. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:30 / 42
页数:13
相关论文
共 170 条
[1]   Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations [J].
Abramov, Andrey Y. ;
Smulders-Srinivasan, Tora K. ;
Kirby, Denise M. ;
Acin-Perez, Rebeca ;
Antonio Enriquez, Jose ;
Lightowlers, Robert N. ;
Duchen, Michael R. ;
Turnbull, Douglass M. .
BRAIN, 2010, 133 :797-807
[2]   Inflammation in osteoarthritis [J].
Goldring, Mary B. ;
Otero, Miguel .
CURRENT OPINION IN RHEUMATOLOGY, 2011, 23 (05) :471-478
[3]   Metabolism in physiological cell proliferation and differentiation [J].
Agathocleous, Michalis ;
Harris, William A. .
TRENDS IN CELL BIOLOGY, 2013, 23 (10) :484-492
[4]   Cycling through metabolism [J].
Aguilar, Victor ;
Fajas, Lluis .
EMBO MOLECULAR MEDICINE, 2010, 2 (09) :338-348
[5]  
Alberts B., 2008, Molecular Biology of the Cell, V5th
[6]   Different responses of astrocytes and neurons to nitric oxide:: The role of glycolytically generated ATP in astrocyte protection [J].
Almeida, A ;
Almeida, J ;
Bolaños, JP ;
Moncada, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (26) :15294-15299
[7]   Nitric oxide switches on glycolysis through the AMP protein kinase and 6-phosphofructo-2-kinase pathway [J].
Almeida, A ;
Moncada, S ;
Bolaños, JP .
NATURE CELL BIOLOGY, 2004, 6 (01) :45-U9
[8]   Reactive oxygen species and endothelial activation [J].
Alom-Ruiz, Sara P. ;
Anilkumar, Narayana ;
Shah, Ajay M. .
ANTIOXIDANTS & REDOX SIGNALING, 2008, 10 (06) :1089-1100
[9]  
Amaral Ana I, 2013, Front Endocrinol (Lausanne), V4, P54, DOI 10.3389/fendo.2013.00054
[10]  
Aoyagi T., 2011, J CELL SCI R, V2012, DOI DOI 10.4172/2157-7013.S5-003