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. 一新穎膜型鳥?酸環化?受體G在生殖系統所扮演的角色功能性分析
 
  • Details
Options

一新穎膜型鳥?酸環化?受體G在生殖系統所扮演的角色功能性分析

Other Title
Functional Characterization of a Novel Receptor Mouse Guanylyl Cyclase G (mGC-G) in Reproduction System
Type
thesis
Date Issued
2006
Author(s)
邱逸雲
Advisor
黃彥華
林美香
Subjects
系所名稱:醫學科學研究所
Abstract
本實驗室在小鼠睪丸中新發現受體型guanylyl cyclase,命名為mGC-G。為了研究其蛋白表現,我們使用抗extracellular domain(ECD)之抗體中和mGC-G作用。由RT-PCR與免疫組織染色證實mGC-G的mRNA與蛋白主要表現在睪丸中的精細胞(spermatid)與精子(spermatozoa);mGC-G也表現於卵巢中的濾泡細胞與卵。利用流式細胞儀與共軛聚焦顯微鏡顯示mGC-G位於精子細胞膜上,分佈在頂體與尾部中段(midpiece)。有趣的是,利用西方墨點法(western blot)顯示睪丸中的mGC-G分子量約為180 kDa,而精子被運輸至附睪後mGC-G被水解成分子量約為48 k Da的蛋白,而表現於成熟精子上。本論文的重點在於研究mGC-G的生理功能。我們分別利用體外的細胞實驗與mGC-G基因剔除鼠來做近一步探討:(一)體外細胞培養實驗部份,我們使用抗ECD之抗體(anti-ECD Ab)來中和mGC-G作用而達到抑制的效果。精子受到牛的血清蛋白(BSA)刺激而活化,產生[Ca2+]i上升,蛋白質磷酸化(protein tyrosine phosphorylation),泳動力增加。預先與anti-ECD Ab培養的精子,再加入BSA刺激後,其[Ca2+]i上升,蛋白質磷酸化(protein tyrosine phosphorylation),泳動力增加等現象皆受到明顯的抑制。(二)建立mGC-G基因剔除鼠來更進一步研究mGC-G在活體內的功能,mGC-G-/-小鼠發育並無明顯異常,然而在自然狀況下的生育力,null mice互相交配顯示其生殖力受到抑制。而在體外授精(in vitro fertilization)的實驗中,null mice的排卵數量與野生型無明顯差異,但null公鼠精子與null母鼠卵子結合,其受精比例明顯下降。綜合以上研究結果顯示,mGC-G表現在睪丸中的精細胞與精子,而在運送到附睪末端後mGC-G受到水解修飾,表現於成熟精子細胞膜上。在生理活性的部份,mGC-G可能參與精子之訊息傳遞,影響精子之泳動力,與[Ca2+]i調控及磷酸化現象的產生有關。而將mGC-G的基因剔除,造成mGC-G基因剔除鼠生育力受損,顯示mGC-G在生殖生理的訊息傳遞上扮演重要的角色。
URI
https://203.71.86.71/handle/123456789/12368

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