共 43 条
New directions for neurodegenerative disease therapy - Using chemical compounds to boost the formation of mutant protein inclusions
被引:25
作者:

Bodner, Ruth A.
论文数: 0 引用数: 0
h-index: 0
机构: MIT, Ctr Canc Res, Cambridge, MA 02139 USA

Housman, David E.
论文数: 0 引用数: 0
h-index: 0
机构: MIT, Ctr Canc Res, Cambridge, MA 02139 USA

Kazantsev, Aleksey G.
论文数: 0 引用数: 0
h-index: 0
机构: MIT, Ctr Canc Res, Cambridge, MA 02139 USA
机构:
[1] MIT, Ctr Canc Res, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Charlestown, MA USA
[3] Massachusetts Gen Hosp, Charlestown, MA USA
[4] MassGen Inst Neurodegenerat Dis, Charlestown, MA USA
来源:
关键词:
Huntington's disease;
Parkinson's disease;
neurodegenerative diseases;
aggregation;
inclusion body;
misfolded protein;
D O I:
10.4161/cc.5.14.2929
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Neurodegenerative diseases such as Huntington's, Parkinson's and Alzheimer's diseases are marked by neuronal accumulation of toxic misfolded protein. Developing therapies for these misfolding diseases requires finding chemical compounds that can either clear toxic misfolded protein, or can protect neurons from their impact. Such compounds could not only provide the starting points for potential drugs, but could also provide valuable research tools for untangling the complexities of the disease process. Until now, chemical screens for these diseases have focused on finding compounds that prevent aggregation of mutant protein. We recently published a compound, B2, which promotes the formation of large inclusions by mutant Huntingtin and alpha-synuclein, while rescuing some of the toxic effects of these proteins. As inclusions were long believed to be toxic to cells, this contradicts previous therapeutic approaches. At the same time, the results support growing evidence for the protective effects of inclusions. In this review, we discuss these results, and place them in the context of ongoing therapeutic discovery efforts for Huntington's disease and other neurodegenerative diseases.
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页码:1477 / 1480
页数:4
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