Repository logo
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
Repository logo
    Communities & Collections
    Research Outputs
    Fundings & Projects
    People
    Organizations
    Statistics
  • English
  • 中文
  • Log In
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. .TMU Publications / 北醫出版品(教師升等著作 / 教學實踐 / 學位論文)
  3. .博碩士學位論文
  4. .94學年度
  5. 大腦皮質神經元發育期間生長相關蛋白GAP-43與Gephyrin之相互作用探討
 
  • Details
Options

大腦皮質神經元發育期間生長相關蛋白GAP-43與Gephyrin之相互作用探討

Other Title
Protein-Protein Interaction of GAP-43 and Gephyrin in Developing Cortical Neurons
Type
thesis
Date Issued
2006
Author(s)
許玉停
Advisor
李怡萱
Subjects
系所名稱:醫學科學研究所
Abstract
摘要 生長相關蛋白(Growth association protein 43 ;GAP-43) 是一種位於突觸前末梢的蛋白,在神經發育以及神經修復過程中參與軸突的延伸、以及引導生長錐生長方向。先前的研究發現,PKC可促進GAP-43的磷酸化,進而對神經生長以及細胞可塑性有促進的作用。我們使用免疫沉澱和質譜儀(MALTI-TOF)的實驗方法,發現GAP-43會與一個位於突觸後膜上,具有聚集抑制性受器功能的蛋白質—gephyrin結合。Gephyrin藉著與glycine receptor ? subunit 以及GABAA receptor??2 subunit結合,來聚集glycine 及GABAA receptor。我們的實驗顯示在畸胎瘤分化的神經細胞或是發育中的大腦皮質神經元細胞, 其細胞膜表面皆可發現有gephnyrin的表現及聚集現象。然而,我們更進一步探討PKC抑制劑Ro-318220對於GAP-43以及gephyrin表現量的影響,結果發現,Ro-318220會增加發育初期的神經細胞(4 DIV)GAP-43的表現量,但在發育晚期神經細胞 (8 DIV)則有抑制的效果。Ro-318220對於gephyrin的表現則無顯著的影響。再者,在共同免疫沉澱(co-immunoprecipitation)的實驗結果發現,投予發育中的神經細胞Ro-318220 24小時會增加GAP-43和gephyrin結合的程度,且在共軛螢光免疫雙染的實驗中亦發現,PKC抑制劑會使GAP-43集中在細胞體,並與gephyrin有共位(colocolization)的現象。反之,Ro-318220會造成gephyrin與GABAAR??2 subunit的結合程度降低,而且,我們進一步發現給予Ro-318220會造成GABA在發育神經元所引發的胞內鈣離子濃度升高反應消失。以上結果顯示,GAP-43受PKC調控的活性,不但會影響神經生長,也可能會藉著與gephyrin的交互作用,影響GABAA receptor的功能。
URI
https://203.71.86.71/handle/123456789/12374
https://hdl.handle.net/11296/6c7btc
File(s)
No Thumbnail Available
Name

C0178874.pdf

Size

8.93 MB

Format

Adobe PDF

Checksum

(MD5):9e56c50902fb12c92302e7b691978007

Copyright Notice

● The digital content on this platform is part of the Taipei Medical University Institutional Repository, featuring various academic works and outputs from the institution. It offers free access to academic research and public education for non-commercial use.

● Please use the content appropriately and within legal boundaries to respect copyright owners' rights. For commercial use, please obtain prior authorization from the copyright owner. Users must not use TMUIR for any illegal purposes.

● By utilising the platform, users are deemed to have fully accepted and understood all the regulations set out in this statement, relevant laws of the Republic of China, all international internet regulations, and usage conventions.

● TMUIR is committed to protecting the interests of copyright owners. If you believe that any material on this website infringes copyright, please contact our staff at libirtmu@gmail.com, and we will remove the work from the repository.

Built with DSpace-CRIS software - Extension maintained and optimized by 4Science

  • Cookie settings
  • Privacy policy
  • End User Agreement
  • Send Feedback