Neurodegenerative diseases associated with the disruption of proteostasis and their therapeutic strategies using chemical chaperones

被引:2
|
作者
Sugiyama, Takashi [1 ,2 ,3 ]
Nishitoh, Hideki [1 ,4 ]
机构
[1] Univ Miyazaki, Fac Med, Lab Biochem & Mol Biol, 5200 Kihara, Kiyotake, Miyazaki 8891692, Japan
[2] Univ Miyazaki Hosp, Fac Med, Dept Neurol, 5200 Kihara, Kiyotake, Miyazaki 8891692, Japan
[3] Univ Miyazaki, Fac Med, Dept Internal Med, Div Respirol Rheumatol Infect Dis & Neurol, 5200 Kihara, Kiyotake, Miyazaki 8891692, Japan
[4] Univ Miyazaki, Frontier Sci Res Ctr, 5200 Kihara, Kiyotake, Miyazaki 8891692, Japan
关键词
4-PBA; chaperone; COPII vesicles; endoplasmic reticulum; neurodegenerative diseases; 4-PHENYLBUTYRIC ACID; STRESS; AGGREGATION; EXPRESSION; PROTEINS; DEATH;
D O I
10.1093/jb/mvae048
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
Aberrant proteostasis is thought to be involved in the pathogenesis of neurodegenerative diseases. Some proteostasis abnormalities are ameliorated by chaperones. Chaperones are divided into three groups: molecular, pharmacological and chemical. Chemical chaperones intended to alleviate stress in organelles, such as the endoplasmic reticulum (ER), are now being administered clinically. Of the chemical chaperones, 4-phenylbutyrate (4-PBA) has been used as a research reagent, and its mechanism of action includes chaperone effects and the inhibition of histone deacetylase. Moreover, it also binds to the B-site of SEC24 and regulates COPII-mediated transport from the ER. Although its therapeutic effect may not be strong, elucidating the mechanism of action of 4-PBA may contribute to the identification of novel therapeutic targets for neurodegenerative diseases. Graphical Abstract
引用
收藏
页码:179 / 186
页数:8
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