Mechanisms of disease: astrocytes in neurodegenerative disease

被引:646
作者
Maragakis, Nicholas J.
Rothstein, Jeffrey D.
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Program Cellular & Mol Med, Baltimore, MD 21287 USA
来源
NATURE CLINICAL PRACTICE NEUROLOGY | 2006年 / 2卷 / 12期
关键词
astrocytes; glia; glial fibrillary acidic protein; glutamate; neurodegenerative disease;
D O I
10.1038/ncpneuro0355
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The term neurodegenerative disease refers to the principal pathology associated with disorders such as amyotrophic lateral sclerosis, Alzheimer's disease, Huntington's disease and Parkinson's disease, and it is presumed that neurodegeneration results in the clinical findings seen in patients with these diseases. Decades of pathological and physiological studies have focused on neuronal abnormalities in these disorders, but it is becoming increasingly evident that astrocytes are also important players in these and other neurological disorders. Our understanding of the normative biology of astrocytes has been aided by the development of animal models in which astrocyte-specific proteins and pathways have been manipulated, and mouse models of neurodegenerative diseases have also revealed astrocyte-specific pathologies that contribute to neurodegeneration. These models have led to the development of targeted therapies for pathways in which astrocytes participate, and this research should ultimately influence the clinical treatment of neurodegenerative disorders.
引用
收藏
页码:679 / 689
页数:11
相关论文
共 68 条
  • [51] Intranigral infusion of interleukin-1β activates astrocytes and protects from subsequent 6-hydroxydopamine neurotoxicity
    Saura, J
    Parés, M
    Bové, J
    Pezzi, S
    Alberch, J
    Marin, C
    Tolosa, E
    Martí, MJ
    [J]. JOURNAL OF NEUROCHEMISTRY, 2003, 85 (03) : 651 - 661
  • [52] Alzheimer's disease: Genes, proteins, and therapy
    Selkoe, DJ
    [J]. PHYSIOLOGICAL REVIEWS, 2001, 81 (02) : 741 - 766
  • [53] Expression of mutant huntingtin in glial cells contributes to neuronal excitotoxicity
    Shin, JY
    Fang, ZH
    Yu, ZX
    Wang, CE
    Li, SH
    Li, XJ
    [J]. JOURNAL OF CELL BIOLOGY, 2005, 171 (06) : 1001 - 1012
  • [54] The neurobiology of glia in the context of water and ion homeostasis
    Simard, M
    Nedergaard, M
    [J]. NEUROSCIENCE, 2004, 129 (04) : 877 - 896
  • [55] Huntingtin protein colocalizes with lesions of neurodegenerative diseases: An investigation in Huntington's, Alzheimer's, and Pick's diseases
    Singhrao, SK
    Thomas, P
    Wood, JD
    MacMillan, JC
    Neal, JW
    Harper, PS
    Jones, AL
    [J]. EXPERIMENTAL NEUROLOGY, 1998, 150 (02) : 213 - 222
  • [56] Connexin43 null mutation increases infarct size after stroke
    Siushansian, R
    Bechberger, JF
    Cechetto, DF
    Hachinski, VC
    Naus, CCG
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 440 (04) : 387 - 394
  • [57] Reactive astrocytes in neural repair and protection
    Sofroniew, MV
    [J]. NEUROSCIENTIST, 2005, 11 (05) : 400 - 407
  • [58] Astrocyte-mediated control of cerebral blood flow
    Takano, T
    Tian, GF
    Peng, WG
    Lou, NH
    Libionka, W
    Han, XN
    Nedergaard, M
    [J]. NATURE NEUROSCIENCE, 2006, 9 (02) : 260 - 267
  • [59] Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1
    Tanaka, K
    Watase, K
    Manabe, T
    Yamada, K
    Watanabe, M
    Takahashi, K
    Iwama, H
    Nishikawa, T
    Ichihara, N
    Hori, S
    Takimoto, M
    Wada, K
    [J]. SCIENCE, 1997, 276 (5319) : 1699 - 1702
  • [60] Cellular pathology of Parkinson's disease: astrocytes, microglia and inflammation
    Teismann, P
    Schulz, JB
    [J]. CELL AND TISSUE RESEARCH, 2004, 318 (01) : 149 - 161