Yin and Yang: complement activation and regulation in Alzheimer's disease

被引:73
作者
Shen, Y
Meri, S
机构
[1] Sun Hlth Res Inst, Haldeman Lab Mol & Cellular Neurobiol, Sun City, AZ 85351 USA
[2] Univ Helsinki, Haartman Inst, Dept Bacteriol & Immunol, FIN-00014 Helsinki, Finland
[3] Arizona State Univ, Mol & Cellular Biol Program, Tempe, AZ 85351 USA
关键词
D O I
10.1016/j.pneurobio.2003.08.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The spectrum of inflammatory diseases is nowadays considered to include diverse diseases of the central nervous system (CNS). Current evidence suggests that syndromes such as Alzheimer's disease (AD) have important inflammatory and immune components and may be amenable to treatment by anti-inflammatory and immunotherapeutic approaches. Compelling evidence has been reported that complement activation occurs in the brain with Alzheimer's disease, and that this contributes to the development of a local inflammatory state that is correlated with cognitive dysfunction. The complement system is a critical element of the innate immune system recognizing and killing, or targeting for destruction, otherwise pathogenic organisms. In addition to triggering the generation of a membranolytic complex, complement proteins interact with cell surface receptors to promote a local inflammatory response that contributes to the protection and healing of the host. Complement activation causes inflammation and cell damage, yet it is an essential component in trying to eliminate cell debris and potentially toxic protein aggregates. It is the balance of these seemingly competing events-the "Yin" and the "Yang"-that influences the ultimate state of neuronal function. Knowledge of the unique molecular interactions that occur in the development of Alzheimer's disease, the functional consequences of those interactions, and the proportional contribution of each element to this disorder, should facilitate the design of effective therapeutic strategies for this disease. (C) 2003 Elsevier Ltd. All rights reserved.
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收藏
页码:463 / 472
页数:10
相关论文
共 110 条
  • [1] Localization and cell association of C1q in Alzheimer's disease brain
    Afagh, A
    Cummings, BJ
    Cribbs, DH
    Cotman, CW
    Tenner, AJ
    [J]. EXPERIMENTAL NEUROLOGY, 1996, 138 (01) : 22 - 32
  • [2] ALMEDA S, 1983, J BIOL CHEM, V258, P785
  • [3] ROLE OF THE BETA-AMYLOID PRECURSOR PROTEIN IN ALZHEIMERS-DISEASE
    ASHALL, F
    GOATE, AM
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1994, 19 (01) : 42 - 46
  • [4] Imaging of amyloid-β deposits in brains of living mice permits direct observation of clearance of plaques with immunotherapy
    Backskai, BJ
    Kajdasz, ST
    Christie, RH
    Carter, C
    Games, D
    Seubert, P
    Schenk, D
    Hyman, BT
    [J]. NATURE MEDICINE, 2001, 7 (03) : 369 - 372
  • [5] Peripherally administered antibodies against amyloid β-peptide enter the central nervous system and reduce pathology in a mouse model of Alzheimer disease
    Bard, F
    Cannon, C
    Barbour, R
    Burke, RL
    Games, D
    Grajeda, H
    Guido, T
    Hu, K
    Huang, JP
    Johnson-Wood, K
    Khan, K
    Kholodenko, D
    Lee, M
    Lieberburg, I
    Motter, R
    Nguyen, M
    Soriano, F
    Vasquez, N
    Weiss, K
    Welch, B
    Seubert, P
    Schenk, D
    Yednock, T
    [J]. NATURE MEDICINE, 2000, 6 (08) : 916 - 919
  • [6] Bird T D, 1987, Alzheimer Dis Assoc Disord, V1, P251, DOI 10.1097/00002093-198701040-00004
  • [7] INHIBITION OF COMPLEMENT ACTIVATION BY NATURAL SULFATED POLYSACCHARIDES (FUCANS) FROM BROWN SEAWEED
    BLONDIN, C
    FISCHER, E
    BOISSONVIDAL, C
    KAZATCHKINE, MD
    JOZEFONVICZ, J
    [J]. MOLECULAR IMMUNOLOGY, 1994, 31 (04) : 247 - 253
  • [8] Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies
    Botto, M
    Dell'Agnola, C
    Bygrave, AE
    Thompson, EM
    Cook, HT
    Petry, F
    Loos, M
    Pandolfi, PP
    Walport, MJ
    [J]. NATURE GENETICS, 1998, 19 (01) : 56 - 59
  • [9] Increased fibrillar β-amyloid in response to human C1q injections into hippocampus and cortex of APP+PS1 transgenic mice
    Boyett, KW
    DiCarlo, G
    Jantzen, PT
    Jackson, J
    O'Leary, C
    Wilcock, D
    Morgan, D
    Gordon, MN
    [J]. NEUROCHEMICAL RESEARCH, 2003, 28 (01) : 83 - 93
  • [10] Complement-dependent proinflammatory properties of the Alzheimer's disease β-peptide
    Bradt, BM
    Kolb, WP
    Cooper, NR
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (03) : 431 - 438