政大機構典藏-National Chengchi University Institutional Repository(NCCUR):Item 140.119/55516
English  |  正體中文  |  简体中文  |  Post-Print筆數 : 27 |  全文笔数/总笔数 : 113656/144643 (79%)
造访人次 : 51724878      在线人数 : 391
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧：
  • 您可在西文检索词汇前后加上"双引号"，以获取较精准的检索结果
  • 若欲以作者姓名搜寻，建议至进阶搜寻限定作者字段，可获得较完整数据
    •  进阶搜寻


    请使用永久网址来引用或连结此文件: https://nccur.lib.nccu.edu.tw/handle/140.119/55516


    题名: 蛋白激脢之細胞訊息傳遞路徑中DARPP-32蛋白所扮演的角色---對大鼠學習記憶和抗細胞凋亡機制的影響
    其它题名: Role and Mechanism of DARPP-32 in Protein Kinase CK2-Mediated Signaling Pathway---Influence on Learning &Amp;Memory and Anti-Apoptosis
    作者: 趙知章
    贡献者: 國立政治大學生命科學研究所
    行政院國家科學委員會
    关键词: 基礎醫學;生物技術;蛋白激脢;細胞訊息傳遞路徑;DARPP-32蛋白;大鼠;學習記憶;抗細胞凋亡
    日期: 2009
    上传时间: 2012-11-15 11:23:45 (UTC+8)
    摘要: 蛋白激酶CK2是屬於一種serine/threonine類的蛋白激酶，CK2與抗細胞凋亡相關的議題已被廣泛探討，這些研究報告指出CK2可以經由活化Akt/PKB、NF-B和ARC蛋白（apoptosis repressor with caspase recruitment domain）等機制來促進細胞的存活。蛋白dopamine and cyclic AMP-regulated phosphoprotein, Mr. 32kDa（DARPP-32）最初是在紋狀體腦區中被發現的，主要受到來自多巴胺的刺激增加了細胞內cAMP的含量進而活化Protein kinase A對DARPP-32蛋白進行磷酸化作用，除此之外，細胞內其他一些激酶如CK2、CK1和Cdk5也會對DARPP-32進行磷酸化作用，近年來的研究指出DARPP-32除了與藥物成癮的生理現象有關外，應該還參與在其他生理調控或改變的機制之中，諸如：DARPP-32和其isoform tDARPP也在腸胃癌細胞內被發現有較高的表現量而且可以減緩癌細胞的死亡，因此DARPP-32也有參與在抗細胞凋亡機制之中的可能性。由於DARPP-32是CK2磷酸化作用的其中一個受質，而我們最近的研究也發現CK2參與在BDNF抗細胞凋亡的機制之中，承續這個研究結果，本研究計畫今年度的研究重點在確立CK2/DARPP-32/Bcl-xL訊息傳遞路徑的相關性和調控CK2活性或DARPP-32表現是否可拮抗興奮性神經毒性物質對神經細胞的傷害。
    Protein kinase CK2 is a multifunctional and ubiquitous serine/threonine protein kinase. Many studies of CK2 are focused on its anti-apoptotic effects. There are many reports showing that CK2 could activate protein kinase Akt, NF-B and ARC protein (apoptosis repressor with caspase recruitment domain) and to enhance cell survival. Meanwhile, the dopamine and cyclic AMP-regulated phosphoprotein, Mr. 32kDa (DARPP-32) was originally found to be activated by dopamine and cAMP through PKA-dependent phosphorylation in the striatum. DARPP-32 was also found to be phosphorylated by other kinase such as CK2, Ck1 and Cdk5. Beside it well-known role in drug addiction, recent studies indicated that DARPP-32 might also involve in other physiological functions. The higher protein expression of DARPP-32 and its isoform tDARPP were found in the gastrointestinal carcinomas and were relative to maintain the cell survival. In our past study, we found that CK2 activation was involved in the anti-apoptotic effects of BDNF in the recent study. Since the DARPP-32 is one of substrates for CK2 phosphorylation, the present study is aimed to investigate the role of and mechanism of DARPP-32 involved in the CK2-mediated signaling pathway. The specific aims of this year are as following: (1) to investigate whether the relationships between CK2, DARPP-32 and Bcl-xL exist in the hippocampal CA1 regions of rats in the anti-apoptotic mechanism; (2) to clarify whether manipulation of CK2 activity and DARPP-32 phosphorylation status will influence the anti-apoptotic effects against excitotoxicity.
    關聯: 基礎研究
    學術補助
    研究期間:9808~ 9907
    研究經費: 1100仟元
    数据类型: report
    显示于类别:[神經科學研究所] 國科會研究計畫

    文件中的档案:

    档案 大小格式浏览次数
    index.html0KbHTML2962检视/开启


    在政大典藏中所有的数据项都受到原著作权保护.


    社群 sharing

    著作權政策宣告 Copyright Announcement
    1.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.
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈