Geldanamycin activates a heat shock response and inhibits huntingtin aggregation in a cell culture model of Huntington's disease

被引:357
作者
Sittler, A
Lurz, R
Lueder, G
Priller, J
Hayer-Hartl, MK
Hartl, FU
Lehrach, H
Wanker, EE
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[2] Humboldt Univ, Dept Neurol, Charite, D-10117 Berlin, Germany
[3] Max Planck Inst Biochem, Abt Zellulare Biochem, D-82152 Martinsried, Germany
关键词
D O I
10.1093/hmg/10.12.1307
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
Huntington's disease (HD) is a progressive neurodegenerative disorder with no effective treatment, Geldanamycin is a benzoquinone ansamycin that binds to the heat shock protein Hsp90 and activates a heat shock response in mammalian cells. In this study, we show by using a filter retardation assay and immunofluorescence microscopy that treatment of mammalian cells with geldanamycin at nanomolar concentrations induces the expression of Hsp40, Hsp70 and Hsp90 and inhibits HD exon 1 protein aggregation in a dose-dependent manner. Similar results were obtained by overexpression of Hsp70 and Hsp40 in a separate cell culture model of HD, This is the first demonstration that huntingtin protein aggregation in cells can be suppressed by chemical compounds activating a specific heat shock response. These findings may provide the basis for the development of a novel pharmacotherapy for HD and related glutamine repeat disorders.
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收藏
页码:1307 / 1315
页数:9
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共 38 条
  • [1] Mechanisms of chaperone suppression of polyglutamine disease:: selectivity, synergy and medullation of protein solubility in Drosophila
    Chan, HYE
    Warrick, JM
    Gray-Board, GL
    Paulson, HL
    Bonini, NM
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (19) : 2811 - 2820
  • [2] Chavany C, 1996, J BIOL CHEM, V271, P4974
  • [3] Chaperone suppression of aggregation and altered subcellular proteasome localization imply protein misfolding in SCA1
    Cummings, CJ
    Mancini, MA
    Antalffy, B
    DeFranco, DB
    Orr, HT
    Zoghbi, HY
    [J]. NATURE GENETICS, 1998, 19 (02) : 148 - 154
  • [4] Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
    Davies, SW
    Turmaine, M
    Cozens, BA
    DiFiglia, M
    Sharp, AH
    Ross, CA
    Scherzinger, E
    Wanker, EE
    Mangiarini, L
    Bates, GP
    [J]. CELL, 1997, 90 (03) : 537 - 548
  • [5] Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
    DiFiglia, M
    Sapp, E
    Chase, KO
    Davies, SW
    Bates, GP
    Vonsattel, JP
    Aronin, N
    [J]. SCIENCE, 1997, 277 (5334) : 1990 - 1993
  • [6] DiFiglia M, 1997, AM J PSYCHIAT, V154, P1046
  • [7] HIGH-EFFICIENCY GENE-TRANSFER INTO MAMMALIAN-CELLS
    GORMAN, CM
    LANE, DP
    RIGBY, PWJ
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1984, 307 (1132) : 343 - &
  • [8] Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: Implications for Huntington's disease therapy
    Heiser, V
    Scherzinger, E
    Boeddrich, A
    Nordhoff, E
    Lurz, R
    Schugardt, N
    Lehrach, H
    Wanker, EE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (12) : 6739 - 6744
  • [9] Aggregation of truncated GST-HD exon 1 fusion proteins containing normal range and expanded glutamine repeats
    Hollenbach, B
    Scherzinger, E
    Schweiger, K
    Lurz, R
    Lehrach, H
    Wanker, EE
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1999, 354 (1386) : 991 - 994
  • [10] Polyglutamine length-dependent interaction of Hsp40 and Hsp70 family chaperones with truncated N-terminal huntingtin: their role in suppression of aggregation and cellular toxicity
    Jana, NR
    Tanaka, M
    Wang, GH
    Nukina, N
    [J]. HUMAN MOLECULAR GENETICS, 2000, 9 (13) : 2009 - 2018