Metal Toxicity Links to Alzheimer's Disease and Neuroinflammation

被引:342
作者
Huat, Tee Jong [1 ,2 ]
Camats-Perna, Judith [1 ]
Newcombe, Estella A. [1 ]
Valmas, Nicholas [3 ]
Kitazawa, Masashi [4 ]
Medeiros, Rodrigo [1 ]
机构
[1] Univ Queensland, Queensland Brain Inst, Clem Jones Ctr Ageing Dementia Res, Neurula Lab, Brisbane, Qld, Australia
[2] Univ Queensland, Ctr Stem Cell Ageing & Regenerat Engn, Brisbane, Qld, Australia
[3] Univ Queensland, Queensland Brain Inst, Brisbane, Qld 4072, Australia
[4] Univ Calif Irvine, Dept Med, Ctr Occupat & Environm Hlth, Irvine, CA 92717 USA
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
AMYLOID PRECURSOR PROTEIN; TRANSGENIC MOUSE MODEL; FOREBRAIN CHOLINERGIC NEURONS; EXACERBATES TAU PATHOLOGY; ADULT LEAD-EXPOSURE; INDUCED CELL-DEATH; A-BETA OLIGOMERS; OXIDATIVE STRESS; NEUROFIBRILLARY DEGENERATION; IRON ACCUMULATION;
D O I
10.1016/j.jmb.2019.01.018
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
As the median age of the population increases, the number of individuals with Alzheimer's disease (AD) and the associated socio-economic burden are predicted to worsen. While aging and inherent genetic predisposition play major roles in the onset of AD, lifestyle, physical fitness, medical condition, and social environment have emerged as relevant disease modifiers. These environmental risk factors can play a key role in accelerating or decelerating disease onset and progression. Among known environmental risk factors, chronic exposure to various metals has become more common among the public as the aggressive pace of anthropogenic activities releases excess amount of metals into the environment. As a result, we are exposed not only to essential metals, such as iron, copper, zinc and manganese, but also to toxic metals including lead, aluminum, and cadmium, which perturb metal homeostasis at the cellular and organismal levels. Herein, we review how these metals affect brain physiology and immunity, as well as their roles in the accumulation of toxic AD proteinaceous species (i.e., beta-amyloid and tau). We also discuss studies that validate the disruption of immune-related pathways as an important mechanism of toxicity by which metals can contribute to AD. Our goal is to increase the awareness of metals as players in the onset and progression of AD. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1843 / 1868
页数:26
相关论文
共 353 条
[1]   Neurobehavioral toxic effects of perinatal oral exposure to aluminum on the developmental motor reflexes, learning, memory and brain neurotransmitters of mice offspring [J].
Abu-Taweel, Gasem M. ;
Ajarem, Jamaan S. ;
Ahmad, Mohammad .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2012, 101 (01) :49-56
[2]   Copper Promotes the Trafficking of the Amyloid Precursor Protein [J].
Acevedo, Karla M. ;
Hung, Ya Hui ;
Dalziel, Andrew H. ;
Li, Qiao-Xin ;
Laughton, Katrina ;
Wikhe, Krutika ;
Rembach, Alan ;
Roberts, Blaine ;
Masters, Colin L. ;
Bush, Ashley I. ;
Camakaris, James .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (10) :8252-8262
[3]   Rapid restoration of cognition in Alzheimer's transgenic mice with 8-hydroxy quinoline analogs is associated with decreased interstitial Aβ [J].
Adlard, Paul A. ;
Cherny, Robert A. ;
Finkelstein, David I. ;
Gautier, Elisabeth ;
Robb, Elysia ;
Cortes, Mikhalina ;
Volitakis, Irene ;
Liu, Xiang ;
Smith, Jeffrey P. ;
Perez, Keyla ;
Laughton, Katrina ;
Li, Qiao-Xin ;
Charman, Susan A. ;
Nicolazzo, Joseph A. ;
Wilkins, Simon ;
Deleva, Karolina ;
Lynch, Toni ;
Kok, Gaik ;
Ritchie, Craig W. ;
Tanzi, Rudolph E. ;
Cappai, Roberto ;
Masters, Colin L. ;
Barnham, Kevin J. ;
Bush, Ashley I. .
NEURON, 2008, 59 (01) :43-55
[4]   Metal chaperones prevent zinc-mediated cognitive decline [J].
Adlard, Paul A. ;
Parncutt, Jacqui ;
Lal, Varsha ;
James, Simon ;
Hare, Dominic ;
Doble, Philip ;
Finkelstein, David I. ;
Bush, Ashley I. .
NEUROBIOLOGY OF DISEASE, 2015, 81 :196-202
[5]   Metal Ionophore Treatment Restores Dendritic Spine Density and Synaptic Protein Levels in a Mouse Model of Alzheimer's Disease [J].
Adlard, Paul A. ;
Bica, Laura ;
White, Anthony R. ;
Nurjono, Milawaty ;
Filiz, Gulay ;
Crouch, Peter J. ;
Donnelly, Paul S. ;
Cappai, Roberto ;
Finkelstein, David I. ;
Bush, Ashley I. .
PLOS ONE, 2011, 6 (03)
[6]   Induction of neuronal apoptosis by thiol oxidation: Putative role of intracellular zinc release [J].
Aizenman, E ;
Stout, AK ;
Harnett, KA ;
Dineley, KE ;
McLaughlin, B ;
Reynolds, IJ .
JOURNAL OF NEUROCHEMISTRY, 2000, 75 (05) :1878-1888
[7]   Cadmium-induced effects on bone in a population-based study of women [J].
Akesson, Agneta ;
Bjellerup, Per ;
Lundh, Thomas ;
Lidfeldt, Jonas ;
Nerbrand, Christina ;
Samsioe, Goran ;
Skerfving, Staffan ;
Vahter, Marie .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2006, 114 (06) :830-834
[8]  
Akinrinade Ibukun Dorcas, 2015, Pathophysiology, V22, P39, DOI 10.1016/j.pathophys.2014.12.001
[9]   Long-term oral intake of aluminium or zinc does not accelerate Alzheimer pathology in AßPP and AßPP/tau transgenic mice [J].
Akiyama, Haruhiko ;
Hosokawa, Masato ;
Kametani, Fuyuki ;
Kondo, Hiromi ;
Chiba, Momoko ;
Fukushima, Masako ;
Tabira, Takeshi .
NEUROPATHOLOGY, 2012, 32 (04) :390-397
[10]   Disturbance of cerebral function in people exposed to drinking water contaminated with aluminium sulphate: retrospective study of the Camelford water incident [J].
Altmann, P ;
Cunningham, J ;
Dhanesha, U ;
Ballard, M ;
Thompson, J ;
Marsh, F .
BMJ-BRITISH MEDICAL JOURNAL, 1999, 319 (7213) :807-+