ER stress is the initial response to polyglutamine toxicity in PC12 cells

被引:14
|
作者
Nakayama, Hitoshi [1 ]
Hamada, Masashi [2 ,3 ]
Fujikake, Nobuhiro [4 ]
Nagai, Yoshitaka [4 ]
Zhao, Jing [1 ]
Hatano, Osamu [5 ]
Shimoke, Koji [2 ,3 ]
Isosaki, Minoru [1 ]
Yoshizumi, Masanori [1 ]
Ikeuchi, Toshihiko [2 ,3 ]
机构
[1] Nara Med Univ, Sch Med, Dept Pharmacol, Nara 6348521, Japan
[2] Kansai Univ, Fac Chem Mat & Bioengn, Dept Life Sci & Biotechnol, Neurobiol Lab, Osaka 5648680, Japan
[3] Kansai Univ, High Technol Res Ctr, Osaka 5648680, Japan
[4] Osaka Univ, Grad Sch Med, Dept Med Genet, Div Clin Genet, Suita, Osaka 5650871, Japan
[5] Nara Med Univ, Sch Med, Dept Anat, Nara 6348521, Japan
关键词
ER stress; PC12; cells; Polyglutamine; Proteasome; Ubiquitin; UPS;
D O I
10.1016/j.bbrc.2008.10.006
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
Persistent endoplasmic reticulum (ER) stress and impairment of the ubiquitin-proteasome system (UPS) cause neuronal cell death. However, the relationship between these two phenomena remains controversial. In our current study, we have utilized an expanded polyglutamine fusion Protein (polyQ81) expression system in PC12 cells to further examine the involvement of ER stress and UPS impairment in cell death. The expression of polyQ81-induced ER stress and cell death. PolyQ81 also induced the activation of c-Jun N-terminal kinase (JNK) and caspase-3 and an increase in polyubiquitin immunoreactivity, suggesting UPS impairment. ER stress was induced prior to the accumulation of polyubiquitinated proteins. Low doses of lactacystin had almost similar effects on cell viability and on the activation of JNK and caspase-3 between normal cells and polyQ81-expressing cells. These results suggest that ER stress mediates polyglutamine toxicity prior to UPS impairment during the initial stages of these toxic effects. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:550 / 555
页数:6
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