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  1. NTU Theses and Dissertations Repository
  2. 生命科學院
  3. 生化科學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/76021
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dc.date.accessioned2021-07-01T08:17:18Z-
dc.date.available2021-07-01T08:17:18Z-
dc.date.issued1994
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/76021-
dc.description.abstract近年來在細胞素( cytokine )之訊息傳遞( signal transduction )方面的研究有相當的進展, STAT ( signal transduction and activation of transcription )家族被發現參與許多細胞素的訊息傳遞路徑, STAT 家族具有訊息傳遞以及轉錄活化之雙重功能,其中 ISGF-3α p91 (又名 STAT1α )參與幹擾素 α/β、 γ(IFNα/β、γ)之訊息傳遞路徑,並可調控早期基因( early gene )的表現,為了瞭解 p91 與轉錄因數 AGP/EBP 之間的關係,我製作了抗 P91 之單株抗體,利用抗體為工具,進一步研究 p91 與 AGP/EBP 之間的關係。
此外, mIL-10 為一新的細胞素,關於其訊息傳遞及標的法因的瞭解都不多,雖已知在單核細胞內與 p91 之活化有關,但本論文發現在小白鼠 C127 乳線瘤細胞中仍是由 p91 家族參與傳訊過程。
最後,本論文又試著探討 mIL對 AGP/EBP 基因之調控,發現mIL-10在 C127 細胞中可以促進 AGP 甩 BP 在 RNA 上之表現,所以mIL-10、 P91 與 AGP/EBP 三者之間可能存在著某些微妙的關係。
zh_TW
dc.description.abstractIn recent years, considerable progress has been made on signal transduction pathways of different cytokines. The STAT family of proteins, carrying out dual functions: signal transduction and activation of transcription, are involved in many cytokine-induced signal transductions. p91 (ISGF-3α, STAT1α) was originally identified to be involved in IFN α/β, γ signalling pathway. It has been shown that the activated p91 can stimulate the expression of a set of early genes. In this thesis, anti-p91 monoclonal antibodies were prepared and subsequently used for investigation of IL-10 signal transduction.
The signalling pathway of mIL-10 was studied. mIL-10 can activate p91 in monocytes. It can also induce the translocation of p91 family proteins from cytosol to nucleus in C127 cell.
mIL-10 can induce the expression of AGPIEBP gene. However, the role of p91 in the mIL-10-induced expression of AGP/EBP remains to be clarified.
en
dc.description.provenanceMade available in DSpace on 2021-07-01T08:17:18Z (GMT). No. of bitstreams: 0
Previous issue date: 1994
en
dc.description.tableofcontents中文摘要(Chinese abstract)……………………………………1
英文摘要(English abstract)……………………………………2
第一章 概論(Introduction)……………………………………3
第二章 材料與方法(Materials & Methods)…………………8
一、 選殖人類ISGF-3α, p91片段基因至蛋白質表現載體……8
二、 以鎳離子管柱?Nickel (II) column?純化融合蛋白質……9
三、 抗人類ISGF-3α, p91單秣抗體之製作……………………11
四、 以Baculovirus生產細胞素mouse Interleukin-10………13
五、 老鼠乳線瘤C127細胞核萃取液及細胞質液之抽取……14
六、 免疫沈澱法(Immunoprecipitation)…………………16
七、 聚丙烯醯胺膠體電泳(SDS-PAGE)……………………18
八、 西方墨點法(Western Blot)……………………………21
九、 C127細胞核醣核酸(RNA)之抽取…………………23
十、 北方墨點法(Northern Blot)……………………………24
十一、 細胞轉染(Transfection)…………………………27
十二、 Chloramphenicol Acetyl Transferase(CAT)Assay…28
第三章 實驗結果(Results)…………………………………30
第四章 討論(Discussions)……………………………………52
參考文獻(References)…………………………………………56
dc.language.isozh-TW
dc.title小白鼠細胞素IL-10的訊息傳遞及對轉錄因數AGP/EBP的調控zh_TW
dc.titleSignal Transduction of Mouse Interleukin 10 and Regulation of AGP/EBPen
dc.date.schoolyear82-2
dc.description.degree碩士
dc.relation.page62
dc.rights.note未授權
dc.contributor.author-dept生命科學院zh_TW
dc.contributor.author-dept生化科學研究所zh_TW
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