|
English
|
正體中文
|
简体中文
|
Post-Print筆數 : 27 |
Items with full text/Total items : 113648/144635 (79%)
Visitors : 51582982
Online Users : 940
|
|
|
Loading...
|
Please use this identifier to cite or link to this item:
https://nccur.lib.nccu.edu.tw/handle/140.119/70089
|
Title: | Protein Kinase CK2 Impairs Spatial Memory Formation through Differential Cross Talk with PI-3 Kinase Signaling: Activation of Akt and Inactivation of SGK1 |
Authors: | 趙知章 Chao,Chih Chang;Ma,Yun L.;Lee,Eminy H. Y. |
Contributors: | 神科所 |
Keywords: | protein kinase CK2;serum- and glucocorticoid-inducible kinase 1;Akt;protein phosphatase 2A;spatial memory formation;hippocampus |
Date: | 2007.06 |
Issue Date: | 2014-09-23 12:25:30 (UTC+8) |
Abstract: | Casein kinase II (CK2) is a multifunctional serine/threonine protein kinase that is associated with the development of neuritogenesis and synaptic plasticity. The phosphoinositide 3-kinase (PI-3K)/Akt pathway is implicated in long-term memory formation. In addition, serum- and glucocorticoid-inducible kinase 1 (SGK1) is another downstream target of PI-3K signaling that was shown to play an important role in spatial memory formation. Whether CK2 may also affect memory formation and whether CK2 interacts with Akt and SGK1 during this process is unknown. In the present study, we found that water maze training significantly decreased CK2 activity in the rat hippocampal CA1 area but not inthe dentate gyrus (DG) area. Transfection ofthe dominant negative mutant of CK2, CK2 A156,tothe CA1 area, but not to the DG area, decreased CK2 activity but enhanced spatial memory formation. Meanwhile, it increased SGK1 phosphorylation at Ser422, decreased Akt phosphorylation at Ser473, and increased cAMP response element-binding protein phosphorylation at Ser133. Transfection ofthe constitutively active SGK1, SGKS422D, enhanced whereastransfection ofthe wild-type Aktimpaired spatial memory formation. Also, administration of the protein phosphatase 2A inhibitor, fostriecin, reversed the memory-impairing effect of CK2 WT. It also reversed the effect of CK2 WT in decreasing SGK1 phosphorylation. Akt Ser473 phosphorylation was moderately increased by CK2 WT and fostriecin treatment, but AktS473A mutant transfection reversed the memory-impairing effect of CK2 WT. These results together suggest that CK2 impairs spatial memory formation through differential cross talk with PI-3 kinase signaling by activation of Akt and inactivation of SGK1 through protein phosphatase 2A. |
Relation: | The Journal of Neuroscience,27(23),6243-6248 |
Data Type: | article |
DOI 連結: | http://dx.doi.org/10.1523/JNEUROSCI.1531-07.2007 |
DOI: | 10.1523/JNEUROSCI.1531-07.2007 |
Appears in Collections: | [神經科學研究所] 期刊論文
|
Files in This Item:
File |
Description |
Size | Format | |
6243-6248.pdf | | 364Kb | Adobe PDF2 | 981 | View/Open |
|
All items in 政大典藏 are protected by copyright, with all rights reserved.
|
著作權政策宣告 Copyright Announcement1.本網站之數位內容為國立政治大學所收錄之機構典藏,無償提供學術研究與公眾教育等公益性使用,惟仍請適度,合理使用本網站之內容,以尊重著作權人之權益。商業上之利用,則請先取得著作權人之授權。
The digital content of this website is part of National Chengchi University Institutional Repository. It provides free access to academic research and public education for non-commercial use. Please utilize it in a proper and reasonable manner and respect the rights of copyright owners. For commercial use, please obtain authorization from the copyright owner in advance.
2.本網站之製作,已盡力防止侵害著作權人之權益,如仍發現本網站之數位內容有侵害著作權人權益情事者,請權利人通知本網站維護人員(
nccur@nccu.edu.tw),維護人員將立即採取移除該數位著作等補救措施。
NCCU Institutional Repository is made to protect the interests of copyright owners. If you believe that any material on the website infringes copyright, please contact our staff(
nccur@nccu.edu.tw). We will remove the work from the repository and investigate your claim.