Akt up- and down-regulation in response to endoplasmic reticulum stress

被引:84
作者
Hosoi, Toru
Hyoda, Kanae
Okuma, Yasunobu
Nomura, Yasuyuki
Ozawa, Koichiro
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Dept Pharmacotherapy, Minami Ku, Hiroshima 734, Japan
[2] Hokkaido Univ, Grad Sch Pharmaceut Sci, Dept Pharmacol, Sapporo, Hokkaido 060, Japan
[3] Chiba Inst Sci, Fac Pharmaceut Sci, Dept Pharmacol, Chiba 2880025, Japan
[4] Yokohama Coll Pharm, Kanagawa 2450066, Japan
关键词
endoplasmic reticulum stress; phosphatidylinositol; 3-kinase; Akt; glial cell;
D O I
10.1016/j.brainres.2007.03.052
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Endoplasmic reticulum (ER) stress has been implicated in the pathogenesis of CNS diseases such as Alzheimer's disease, Parkinson's disease, and cerebral ischemia. In the present study, we found that Akt activation is regulated dually by ER stress in primary cultured glial cells. We observed that Akt activation was increased by short-term exposure to ER stress but was down-regulated by long-term exposure to ER stress. ER stress-induced Akt activation was mediated through phosphatidylinositol 3-kinase (PI3K) because the PI3K inhibitors, LY294002 and wortmannin, inhibited Akt activation. Moreover, Akt was localized in the ER, as assessed by immunohistochemistry, and ER stress increased microsomally localized Akt activation. These results suggest that Akt plays an important role in stress conditions, which impair ER function. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 31
页数:5
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