Circadian clocks and neurodegenerative diseases: time to aggregate?

被引:97
作者
Hastings, Michael H. [1 ]
Goedert, Michel [1 ]
机构
[1] MRC Lab Mol Biol, Cambridge CB2 0QH, England
基金
英国医学研究理事会;
关键词
ALZHEIMERS-DISEASE; GENE-EXPRESSION; MOUSE MODEL; PHOSPHATASE-ACTIVITIES; MESSENGER-RNA; BRIGHT LIGHT; LEWY BODIES; REM-SLEEP; PROTEIN; TAU;
D O I
10.1016/j.conb.2013.05.004
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The major neurodegenerative diseases are characterised by a disabling loss of the daily pattern of sleep and wakefulness, which may be reflective of a compromise to the underlying circadian clock that times the sleep cycle. At a molecular level, the canonical property of neurodegenerative diseases is aberrant aggregation of otherwise soluble neuronal proteins. They can thus be viewed as disturbances of proteostasis, raising the question whether the two features altered daily rhythms and molecular aggregation are related. Recent discoveries have highlighted the fundamental contribution of circadian clocks to the correct ordering of daily cellular metabolic cycles, imposing on peripheral organs such as the liver a strict programme that alternates between anabolic and catabolic states. The discovery that circadian mechanisms are active in local brain regions suggests that they may impinge upon physiological and pathological elements that influence pro-neurodegenerative aggregation. This review explores how introducing the dimension of circadian time and the circadian clock might refine the analysis of aberrant aggregation, thus expanding our perspective on the cell biology common to neurodegenerative diseases.
引用
收藏
页码:880 / 887
页数:8
相关论文
共 70 条
[1]
Optogenetic deconstruction of sleep-wake circuitry in the brain [J].
Adamantidis, Antoine ;
Carter, Matthew C. ;
de Lecea, Luis .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2010, 2
[2]
Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus [J].
Akhtar, RA ;
Reddy, AB ;
Maywood, ES ;
Clayton, JD ;
King, VM ;
Smith, AG ;
Gant, TW ;
Hastings, MH ;
Kyriacou, CP .
CURRENT BIOLOGY, 2002, 12 (07) :540-550
[3]
Reversible paired helical filament-like phosphorylation of tau is an adaptive process associated with neuronal plasticity in hibernating animals [J].
Arendt, T ;
Stieler, J ;
Strijkstra, AM ;
Hut, RA ;
Rüdiger, J ;
Van der Zee, EA ;
Harkany, T ;
Holzer, M ;
Härtig, W .
JOURNAL OF NEUROSCIENCE, 2003, 23 (18) :6972-6981
[4]
The circadian regulation of presenilin-2 gene expression [J].
Belanger, Valerie ;
Picard, Nathalie ;
Cermakian, Nicolas .
CHRONOBIOLOGY INTERNATIONAL, 2006, 23 (04) :747-766
[5]
Sleep Disturbance in Dementia with Lewy Bodies and Alzheimer's Disease: A Multicenter Analysis [J].
Bliwise, Donald L. ;
Mercaldo, Nathaniel D. ;
Avidan, Alon Y. ;
Boeve, Bradley F. ;
Greer, Sophia A. ;
Kukull, Walter A. .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 2011, 31 (03) :239-246
[6]
Boeve BF, 2013, LANCET NEUROL, V12, P469, DOI 10.1016/S1474-4422(13)70054-1
[7]
The pathological process underlying Alzheimer's disease in individuals under thirty [J].
Braak, Heiko ;
Del Tredici, Kelly .
ACTA NEUROPATHOLOGICA, 2011, 121 (02) :171-181
[8]
Rhythms of mammalian body temperature can sustain peripheral circadian clocks [J].
Brown, SA ;
Zumbrunn, G ;
Fleury-Olela, F ;
Preitner, N ;
Schibler, U .
CURRENT BIOLOGY, 2002, 12 (18) :1574-1583
[9]
Circadian regulation of prion protein messenger RNA in the rat forebrain: A widespread and synchronous rhythm [J].
Cagampang, FRA ;
Whatley, SA ;
Mitchell, AL ;
Powell, JF ;
Campbell, IC ;
Coen, CW .
NEUROSCIENCE, 1999, 91 (04) :1201-1204
[10]
Circadian Clock Gene Expression in Brain Regions of Alzheimer's Disease Patients and Control Subjects [J].
Cermakian, Nicolas ;
Lamont, Elaine Waddington ;
Boudreau, Philippe ;
Boivin, Diane B. .
JOURNAL OF BIOLOGICAL RHYTHMS, 2011, 26 (02) :160-170