p62 modulates Akt activity via association with PKCξ in neuronal survival and differentiation

被引:28
作者
Joung, I [1 ]
Kim, HJ
Kwon, YK
机构
[1] Hanseo Univ, Dept Biol, Chungnam 352820, South Korea
[2] Kyung Hee Univ, Dept Biol, Seoul 130701, South Korea
[3] Kyung Hee Univ, Res Inst Basic Sci, Seoul 130701, South Korea
关键词
Akt; differentiation; neuronal stem cell; p62; PKC xi; survival;
D O I
10.1016/j.bbrc.2005.06.138
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
p62 is a ubiquitously expressed phosphoprotein that interacts with a number of signaling molecules and a major component of neurofibrillary tangles in the brain of Alzheimer's disease patients. It has been implicated in important cellular functions Such as cell proliferation and anti-apoptotic pathways. In this study, we have addressed the potential role of p62 during neuronal differentiation and survival using HiB5, a rat neuronal progenitor cell. We generated a recombinant adenovirus encoding T7-epitope tagged p62 to reliably transfer p62 cDNA into the neuronal cells. The results show that an overexpression of p62 led not only to neuronal differentiation, but also to decreased cell death induced by serum withdrawal in HiB5 cells. In this process p62-dependent Akt phosphorylation occurred via the release of Akt from PKC xi by association of p62 and PKC xi, which is known as a negative regulator of Akt activation. These findings indicate that p62 facilitates cell survival through novel signaling cascades that result in Akt activation. Furthermore, we found that p62 expression was induced during neuronal differentiation. Taken together, the data suggest p62 is a regulator of neuronal cell survival and differentiation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:654 / 660
页数:7
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