Does my mouse have Alzheimer's disease?

被引:95
作者
Dodart, JC [1 ]
Mathis, C
Bales, KR
Paul, SM
机构
[1] Eli Lilly & Co, Neurosci Discovery Res, Indianapolis, IN 46285 USA
[2] ULP, IFR Neurosci, CNRS, UMR 7521,Lab Neurosci Comportementales & Cognit, Strasbourg, France
关键词
A beta; Alzheimer's disease; amyloid; APP; behavior; learning and memory; neuropathology; transgenic mouse models;
D O I
10.1034/j.1601-183X.2002.10302.x
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Small animal models that manifest many of the characteristic neuropathological and behavioral features of Alzheimer's disease (AD) have been developed and have proven of great value for studying the pathogenesis of this disorder at the molecular, cellular and behavioral levels. The great progress made in our understanding of the genetic factors that either cause or contribute to the risk of developing AD has prompted many laboratories to create transgenic (tg) mice that overexpress specific genes which cause familial forms of the disease. Several of these tg mice display neuropathological and behavioral features of AD including amyloid beta-peptide (Abeta) and amyloid deposits, neuritic plaques, gliosis, synaptic alterations and signs of neurodegeneration as well as memory impairment. Despite these similarities, important differences in neuropathology and behavior between these tg mouse models and AD have also been observed, and to date no perfect animal model has emerged. Moreover, ascertaining which elements of the neuropathological and behavioral phenotype of these various strains of tg mice are relevant to that observed in AD continues to be a challenge. Here we provide a critical review of the AD-like neuropathology and behavioral phenotypes of several well-known and utilized tg mice that express human APP transgenes.
引用
收藏
页码:142 / 155
页数:14
相关论文
共 125 条
  • [41] Human and murine ApoE markedly alters Aβ metabolism before and after plaque formation in a mouse model of Alzheimer's disease
    Fagan, AM
    Watson, M
    Parsadanian, M
    Bales, KR
    Paul, SM
    Holtzman, DM
    [J]. NEUROBIOLOGY OF DISEASE, 2002, 9 (03) : 305 - 318
  • [42] Ferris SH, 1997, ALZ DIS ASSOC DIS, V11, P45
  • [43] Statistical aspects of quantitative image analysis of β-amyloid in the APPV717F transgenic mouse model of Alzheimer's disease
    Fishman, CE
    Cummins, DJ
    Bales, KR
    DeLong, CA
    Esterman, MA
    Hanson, JC
    White, SL
    Paul, SM
    Jordan, WH
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 2001, 108 (02) : 145 - 152
  • [44] Age-related impairment of synaptic transmission but normal long-term potentiation in transgenic mice that overexpress the human APP695SWE mutant form of amyloid precursor protein
    Fitzjohn, SM
    Morton, RA
    Kuenzi, F
    Rosahl, TW
    Shearman, M
    Lewis, H
    Smith, D
    Reynolds, DS
    Davies, CH
    Collingridge, GL
    Seabrook, GR
    [J]. JOURNAL OF NEUROSCIENCE, 2001, 21 (13) : 4691 - 4698
  • [45] Long-term memory in Alzheimer's disease
    Fleischman, DA
    Gabrieli, J
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 1999, 9 (02) : 240 - 244
  • [46] Frautschy SA, 1998, AM J PATHOL, V152, P307
  • [47] Memory systems analyses of mnemonic disorders in aging and age-related diseases
    Gabrieli, JDE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (24) : 13534 - 13540
  • [48] ALZHEIMER-TYPE NEUROPATHOLOGY IN TRANSGENIC MICE OVEREXPRESSING V717F BETA-AMYLOID PRECURSOR PROTEIN
    GAMES, D
    ADAMS, D
    ALESSANDRINI, R
    BARBOUR, R
    BERTHELETTE, P
    BLACKWELL, C
    CARR, T
    CLEMENS, J
    DONALDSON, T
    GILLESPIE, F
    GUIDO, T
    HAGOPIAN, S
    JOHNSONWOOD, K
    KHAN, K
    LEE, M
    LEIBOWITZ, P
    LIEBERBURG, I
    LITTLE, S
    MASLIAH, E
    MCCONLOGUE, L
    MONTOYAZAVALA, M
    MUCKE, L
    PAGANINI, L
    PENNIMAN, E
    POWER, M
    SCHENK, D
    SEUBERT, P
    SNYDER, B
    SORIANO, F
    TAN, H
    VITALE, J
    WADSWORTH, S
    WOLOZIN, B
    ZHAO, J
    [J]. NATURE, 1995, 373 (6514) : 523 - 527
  • [49] Gene targeting: technical confounds and potential solutions in behavioral brain research
    Gerlai, R
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2001, 125 (1-2) : 13 - 21
  • [50] Behavioral tests of hippocampal function: simple paradigms complex problems
    Gerlai, R
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2001, 125 (1-2) : 269 - 277