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    請使用永久網址來引用或連結此文件: http://libir.tmu.edu.tw/handle/987654321/5874


    題名: 一新穎膜型鳥?酸環化?受體G於人類精子所扮演角色之功能性分析
    Functional Characterization of a Novel Guanylate Cyclase G in Human Spermatozoa
    作者: 吳平
    Ping Wu
    貢獻者: 醫學研究所
    關鍵詞: 鳥苷
    酸環化酶
    人類精子
    guanylate cyclase
    human spermatozoa
    日期: 2006
    上傳時間: 2009-09-11 15:45:53 (UTC+8)
    摘要: 鳥苷酸環化酶(guanylate cyclase, GC)存在兩種類型：水溶性蛋白型鳥苷酸環化酶(soluble guanylate cyclase, sGC)與膜蛋白型鳥苷酸環化酶(particulate guanylate cyclase, pGC)。本實驗室先前的研究成果顯示，GC-G表現於小鼠體內的睪丸組織以及影響成熟精子的生理活性；本論文主題承接先前的研究工作，進一步探討膜蛋白型鳥苷酸環化酶中ㄧ新穎孤兒受體G（GC-G）於人類精子所扮演的角色。
    利用與小鼠鳥苷酸環化脢受體G基因（mGC-G）的同源相似性，我們在人類cDNA library中，發現一段位於第十對染色體的基因，與mGC-G具有高度的相似度，將之命名為human GC-G (hGC-G)。利用Q-PCR與南方墨點法分析結果顯示，hGC-G高度特異地表現於生殖器官中的睪丸。進一步利用預測之hGC-G的extracellular domain中胺基酸序列的一段短肽鏈作為抗原，對兔子進行免疫反應，取得血清進行anti-hGCG IgG之純化，並利用抗體的專一性來進行辨識。實驗結果顯示，hGC-G蛋白表現於人類成熟精子當中；進一步利用共軛焦顯微鏡及流式細胞儀分析，證實hGC-G蛋白為一表現在精子之頂體與尾部中段的膜上型受體；至於功能性的評估方面，我們發現專一性辨識hGC-G的抗體，並未抑止精子獲能相關的酪胺酸磷酸化現象；而在hGC-G extracellular domain中的RGD序列，有效的中和HEK293T細胞膜外的integrin且顯著降低與fibronectin結合的能力。顯示hGC-G的功能可能不參與精子獲能作用之訊息傳遞，而是精卵進行受精作用時，扮演分子之間辨識的角色。
    Guanylyl cyclase (GC) is known to transmit signaling by synthesizing of intracellular cyclic GMP. We have previously described an orphan GC receptor on mouse sperm (mouse GC-G) which is able to regulate sperm motility and capacitation-associated protein tyrosine phosphorylation. Here, we reported the identification and functional characterization of its apparent homologue in humans (hGC-G). By the comparative genomic approach, hGC-G gene is composed of 21 exons, spanning a minimum of 48 kb on chromosome 10q25. When compared with the mouse orthologue, hGC-G showed in the presence of deletions, incomplete splicing of introns, or in-frame termination codons. The real-time quantitative reverse transcriptase (RT)-PCR analysis demonstrated that hGC-G is expressed in human testis, followed by a low expression in placenta, but with no expression in other tissues. Western blotting revealed that hGC-G in sperm composed three isoforms ranged in 30 ~ 45 kDa, and was expressed on the cell surface of spermatozoa by utilizing flow cytometry and confocal immunofluorescent analysis. Furthermore, with hGC-G-RGD peptide and anti-hGC-G antibody neutralizing assay, we found that hGC-G may involve in molecular recognition of sperm (RGD motif of hGC-G on sperm) and oocyte (integrin on oocyte), but not in receptor-transmitted capacitation signalings.
    資料類型: thesis
    顯示於類別:[醫學科學研究所] 博碩士論文

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