OASIS, a CREB/ATF-family member, modulates UPR signalling in astrocytes

被引:246
作者
Kondo, S
Murakami, T
Tatsumi, K
Ogata, M
Kanemoto, S
Otori, K
Iseki, K
Wanaka, A
Imaizumi, K
机构
[1] Miyazaki Univ, Fac Med, Dept Anat, Miyazaki 8891692, Japan
[2] Nara Inst Sci & Technol NAIST, Div Struct Cellular Biol, Nara 6300101, Japan
[3] Nara Med Univ, Dept Anat, Nara 6348522, Japan
[4] Yamagata Univ, Sch Med, Dept Emergency Med, Yamagata 9909585, Japan
基金
日本学术振兴会;
关键词
D O I
10.1038/ncb1213
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endoplasmic reticulum (ER) stress transducers IRE1, PERK and ATF6 are well known to transduce signals from the ER to the cytoplasm and nucleus when unfolded proteins are accumulated in the ER. Here, we identified OASIS as a novel ER stress transducer. OASIS is a basic leucine zipper ( bZIP) transcription factor of the CREB/ATF family with a transmembrane domain that allows it to associate with the ER. The molecule is cleaved at the membrane in response to ER stress, and its cleaved amino-terminal cytoplasmic domain, which contains the bZIP domain, translocates into the nucleus where it activates the transcription of target genes that are mediated by ER stress-responsive and cyclic AMP-responsive elements. Intriguingly, OASIS was induced at the transcriptional level during ER stress in astrocytes of the central nervous system, but not in other cell types examined. Furthermore, overexpression of OASIS resulted in induction of BiP and suppression of ER-stress-induced cell death, whereas knockdown partially reduced BiP levels and led to ER stress in susceptible astrocytes. Our results reveal pivotal roles for OASIS in modulating the unfolded protein response in astrocytes, and the possibility that cell type-specific UPR signalling also exists in other cells.
引用
收藏
页码:186 / U112
页数:13
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