Proteasomes and proteasome inhibition in the central nervous system

被引:99
作者
Ding, QX
Keller, JN
机构
[1] Univ Kentucky, Dept Anat & Neurobiol, Lexington, KY 40536 USA
[2] Univ Kentucky, Dept Gerontol, Lexington, KY USA
[3] Univ Kentucky, Sanders Brown Res Ctr Aging, Lexington, KY USA
关键词
central nervous system; heat shock protein; oxidative stress; proteasome; free radicals;
D O I
10.1016/S0891-5849(01)00635-9
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
Although the proteasome is responsible for the majority of intracellular protein degradation, and has been demonstrated to play a pivotal role in a diverse array of cellular activities, the role of the proteasome in the central nervous system is only beginning to be elucidated. Recent studies have demonstrated that proteasome inhibition occurs in numerous neurodegenerative conditions, and that proteasome inhibition is sufficient to induce neuron death, elevate intracellular levels of protein oxidation, and increase neural vulnerability to subsequent injury. The focus of this review is to describe what is currently known about proteasome biology in the central nervous system and to discuss the possible role of proteasome inhibition in the neurodegenerative process. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:574 / 584
页数:11
相关论文
共 131 条
  • [31] Inhibition of the multicatalytic proteinase (proteasome) by 4-hydroxy-2-nonenal cross-linked protein
    Friguet, B
    Szweda, LI
    [J]. FEBS LETTERS, 1997, 405 (01): : 21 - 25
  • [32] DISPLACEMENT OF HOUSEKEEPING PROTEASOME SUBUNITS BY MHC-ENCODED LMPS - A NEWLY DISCOVERED MECHANISM FOR MODULATING THE MULTICATALYTIC PROTEINASE COMPLEX
    FRUH, K
    GOSSEN, M
    WANG, KN
    BUJARD, H
    PETERSON, PA
    YANG, Y
    [J]. EMBO JOURNAL, 1994, 13 (14) : 3236 - 3244
  • [33] cDNA cloning of p42, a shared subunit of two proteasome regulatory proteins, reveals a novel member of the AAA protein family
    Fujiwara, T
    Watanabe, TK
    Tanaka, K
    Slaughter, CA
    DeMartino, GN
    [J]. FEBS LETTERS, 1996, 387 (2-3) : 184 - 188
  • [34] Activation of the cell death program by nitric oxide involves inhibition of the proteasome
    Glockzin, S
    von Knethen, A
    Scheffner, M
    Brüne, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (28) : 19581 - 19586
  • [35] GLOTZER M, 1991, NATURE, V349, P132, DOI 10.1038/349132a0
  • [36] THE MAJOR HISTOCOMPATIBILITY COMPLEX-ENCODED PROTEASOME COMPONENT LMP7 - ALTERNATIVE 1ST EXONS AND POSTTRANSLATIONAL PROCESSING
    GLYNNE, R
    KERR, LA
    MOCKRIDGE, I
    BECK, S
    KELLY, A
    TROWSDALE, J
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (04) : 860 - 866
  • [37] Goldberg AL, 1997, BIOL CHEM, V378, P131
  • [38] Possible role of NF-κB and p53 in the glutamate-induced pro-apoptotic neuronal pathway
    Grilli, M
    Memo, M
    [J]. CELL DEATH AND DIFFERENTIATION, 1999, 6 (01) : 22 - 27
  • [39] Peroxynitrite increases the degradation of aconitase and other cellular proteins by proteasome
    Grune, T
    Blasig, IE
    Sitte, N
    Roloff, B
    Haseloff, R
    Davies, KJA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (18) : 10857 - 10862
  • [40] Degradation of oxidized proteins in mammalian cells
    Grune, T
    Reinheckel, T
    Davies, KJA
    [J]. FASEB JOURNAL, 1997, 11 (07) : 526 - 534