Targeting protein aggregation for the treatment of degenerative diseases

被引:310
作者
Eisele, Yvonne S. [1 ,2 ]
Monteiro, Cecilia [1 ,2 ]
Fearns, Colleen [2 ]
Encalada, Sandra E. [2 ,3 ,4 ]
Wiseman, R. Luke [2 ,5 ]
Powers, Evan T. [1 ]
Kelly, Jeffery W. [1 ,2 ,6 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dorris Neurosci Ctr, La Jolla, CA 92037 USA
[4] Scripps Res Inst, Dept Mol & Cellular Neurosci, La Jolla, CA 92037 USA
[5] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
[6] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
FAMILIAL AMYLOID POLYNEUROPATHY; HEAT-SHOCK RESPONSE; IMMUNOGLOBULIN LIGHT-CHAIN; CEREBRAL BETA-AMYLOIDOSIS; NUCLEATED CONFORMATIONAL CONVERSION; SENILE SYSTEMIC AMYLOIDOSIS; GAMMA-SECRETASE INHIBITORS; ALPHA-SYNUCLEIN OLIGOMERS; WORLD TRANSPLANT REGISTRY; RECOMBINANT PRION PROTEIN;
D O I
10.1038/nrd4593
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The aggregation of specific proteins is hypothesized to underlie several degenerative diseases, which are collectively known as amyloid disorders. However, the mechanistic connection between the process of protein aggregation and tissue degeneration is not yet fully understood. Here, we review current and emerging strategies to ameliorate aggregation-associated degenerative disorders, with a focus on disease-modifying strategies that prevent the formation of and/or eliminate protein aggregates. Persuasive pharmacological and genetic evidence now supports protein aggregation as the cause of postmitotic tissue dysfunction or loss. However, a more detailed understanding of the factors that trigger and sustain aggregate formation and of the structure activity relationships underlying proteotoxicity is needed to develop future disease-modifying therapies.
引用
收藏
页码:759 / 780
页数:22
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