Nature, nurture and neurology: gene-environment interactions in neurodegenerative disease - FEBS anniversary prize lecture delivered on 27 June 2004 at the 29th FEBS Congress in Warsaw

被引:75
作者
Spires, TL
Hannan, AJ [1 ]
机构
[1] Univ Melbourne, Howard Florey Inst, Natl Inst Neurosci, Parkville, Vic 3010, Australia
[2] Massachusetts Gen Hosp, MassGen Inst Neurodegenerat Dis, Charlestown, MA USA
[3] Harvard Univ, Sch Med, Charlestown, MA USA
关键词
Alzheimer; BDNF; environmental enrichment; Huntington; neurodegeneration;
D O I
10.1111/j.1742-4658.2005.04677.x
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
Neurodegenerative disorders, such as Huntington's, Alzheimer's, and Parkinson's diseases, affect millions of people worldwide and currently there are few effective treatments and no cures for these diseases. Transgenic mice expressing human transgenes for huntingtin, amyloid precursor protein, and other genes associated with familial forms of neurodegenerative disease in humans provide remarkable tools for studying neurodegeneration because they mimic many of the pathological and behavioural features of the human conditions. One of the recurring themes revealed by these various transgenic models is that different diseases may share similar molecular and cellular mechanisms of pathogenesis. Cellular mechanisms known to be disrupted at early stages in multiple neurodegenerative disorders include gene expression, protein interactions (manifesting as pathological protein aggregation and disrupted signaling), synaptic function and plasticity. Recent work in mouse models of Huntington's disease has shown that enriching the environment of transgenic animals delays the onset and slows the progression of Huntington's disease-associated motor and cognitive symptoms. Environmental enrichment is known to induce various molecular and cellular changes in specific brain regions of wild-type animals, including altered gene expression profiles, enhanced neurogenesis and synaptic plasticity. The promising effects of environmental stimulation, demonstrated recently in models of neurodegenerative disease, suggest that therapy based on the principles of environmental enrichment might benefit disease sufferers and provide insight into possible mechanisms of neurodegeneration and subsequent identification of novel therapeutic targets. Here, we review the studies of environmental enrichment relevant to some major neurodegenerative diseases and discuss their research and clinical implications.
引用
收藏
页码:2347 / 2361
页数:15
相关论文
共 145 条
[111]   FAMILIAL ALZHEIMERS-DISEASE IN KINDREDS WITH MISSENSE MUTATIONS IN A GENE ON CHROMOSOME-1 RELATED TO THE ALZHEIMERS-DISEASE TYPE-3 GENE [J].
ROGAEV, EI ;
SHERRINGTON, R ;
ROGAEVA, EA ;
LEVESQUE, G ;
IKEDA, M ;
LIANG, Y ;
CHI, H ;
LIN, C ;
HOLMAN, K ;
TSUDA, T ;
MAR, L ;
SORBI, S ;
NACMIAS, B ;
PIACENTINI, S ;
AMADUCCI, L ;
CHUMAKOV, I ;
COHEN, D ;
LANNFELT, L ;
FRASER, PE ;
ROMMENS, JM ;
STGEORGEHYSLOP, PH .
NATURE, 1995, 376 (6543) :775-778
[112]   Familial influence on age of onset among siblings with Huntington disease [J].
Rosenblatt, A ;
Brinkman, RR ;
Liang, KY ;
Almqvist, EW ;
Margolis, RL ;
Huang, CY ;
Sherr, M ;
Franz, ML ;
Abbott, MH ;
Hayden, MR ;
Ross, CA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (05) :399-403
[113]   Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease [J].
Rubinsztein, DC ;
Leggo, J ;
Chiano, M ;
Dodge, A ;
Norbury, G ;
Rosser, E ;
Craufurd, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3872-3876
[114]   Enriched environment and acceleration of visual system development [J].
Sale, A ;
Putignano, E ;
Cancedda, L ;
Landi, S ;
Cirulli, F ;
Berardi, N ;
Maffei, L .
NEUROPHARMACOLOGY, 2004, 47 (05) :649-660
[115]   Transgenic models of Huntington's disease [J].
Sathasivam, K ;
Hobbs, C ;
Mangiarini, L ;
Mahal, A ;
Turmaine, M ;
Doherty, P ;
Davies, SW ;
Bates, GP .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 354 (1386) :963-969
[116]   ASSOCIATION OF APOLIPOPROTEIN-E ALLELE EPSILON-4 WITH LATE-ONSET FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE [J].
SAUNDERS, AM ;
STRITTMATTER, WJ ;
SCHMECHEL, D ;
GEORGEHYSLOP, PHS ;
PERICAKVANCE, MA ;
JOO, SH ;
ROSI, BL ;
GUSELLA, JF ;
CRAPPERMACLACHLAN, DR ;
ALBERTS, MJ ;
HULETTE, C ;
CRAIN, B ;
GOLDGABER, D ;
ROSES, AD .
NEUROLOGY, 1993, 43 (08) :1467-1472
[117]   Influence of leisure activity on the incidence of Alzheimer's Disease [J].
Scarmeas, N ;
Levy, G ;
Tang, MX ;
Manly, J ;
Stern, Y .
NEUROLOGY, 2001, 57 (12) :2236-2242
[118]   Cognitive reserve: Implications for diagnosis and prevention of Alzheimer's disease [J].
Scarmeas N. ;
Stern Y. .
Current Neurology and Neuroscience Reports, 2004, 4 (5) :374-380
[119]   Environmental, pharmacological, and genetic modulation of the HD phenotype in transgenic mice [J].
Schilling, G ;
Savonenko, AV ;
Coonfield, ML ;
Morton, JL ;
Vorovich, E ;
Gale, A ;
Neslon, C ;
Chan, N ;
Eaton, M ;
Fromholt, D ;
Ross, CA ;
Borchelt, DR .
EXPERIMENTAL NEUROLOGY, 2004, 187 (01) :137-149
[120]  
SELKOE DJ, 1999, ALZHEIMER DIS, P293