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

被引:360
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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页码:1307 / 1315
页数:9
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