Akt phosphorylation is essential for nuclear translocation and retention in NGF-stimulated PC12 cells

被引:60
作者
Nguyen, Truong Le Xuan
Choi, Joung Woo
Lee, Sang Bae
Ye, Keqiang
Woo, Soo-Dong
Lee, Kyung-Hoon
Ahn, Jee-Yin [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Ctr Mol Med,Dept Mol Cell Biol, Suwon 440746, South Korea
[2] Emory Univ, Sch Med, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
[3] Chungbuk Natl Univ, Coll Agr Life & Environm Sci, Dept Plant Med, Cheongju 361763, South Korea
[4] Sungkyunkwan Univ, Dept Anat, Sch Med, Suwon 440746, South Korea
基金
新加坡国家研究基金会;
关键词
Akt; nerve growth factor (NGF); phosphoinositide 3-kinase (PI3K); PC12; cells; phosphorylation;
D O I
10.1016/j.bbrc.2006.08.120
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Nerve growth factor (NGF) elicits Akt translocation into the nucleus, where it phosphorylates nuclear targets. Here, we describe that Akt phosphorylation can promote the nuclear translocation of Akt and is necessary for its nuclear retention. Overexpression of Akt-K179A, T308A, S473A-mutant failed to show either nuclear translocation or nuclear Akt phosphorylation, whereas expression of wild-type counterpart elicited profound Akt phosphorylation and induced nuclear translocation under NGF stimulation. Employing the PI3K inhibitor and a variety of mutants PI3K, we showed that nuclear translocation of Akt was mediated by activation of PI3K, and Akt phosphorylation status in the nucleus required PI3K activity. Thus the activity of PI3K might contribute to the nuclear translocation of Akt, and that Akt phosphorylation is essential for its nuclear retention under NGF stimulation conditions. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:789 / 798
页数:10
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