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    Please use this identifier to cite or link to this item: http://ir.cnu.edu.tw/handle/310902800/27594

    作者: Liu, Shan-Wen
    Cho, Kuan-Hung
    Chen, Mei-Ru
    Yu, Hsiao-Chi
    Kao, Yu-Ying
    Tsou, Tsui-Chun
    Lin, Ching-Po
    Chen, Chin-Tu
    Hsu, Ching-Han
    Lin, Kurt Ming-Chao
    Lin, Kurt Ming-Chao �
    Tsou, Tsui-Chun�
    貢獻者: 生物科技系
    關鍵字: Magnetic Resonance Imaging
    Multimodality Imaging
    Red Fluorescent Protein
    Iron Loading
    日期: 2012-08
    上傳時間: 2014-03-21 16:14:39 (UTC+8)
    出版者: World Scientific Publ Co Pte Ltd
    摘要: In this report, we generated a ferritin and red fluorescent protein fusion reporter gene that enables the visualization of transgene expression in living animals by magnetic resonance imaging (MRI) and optical imaging. Ferritin heavy chain (FTH) or light chain (FTL) was linked to the N terminus of the monomeric DsRed red fluorescent protein to create FTH-DsRed and FTL-DsRed, MRI-fluorescence dual reporters. Transfection of these dual reporters into cells resulted in increased iron loading and strong red fluorescence in cells. Adenoviral vectors to express FTH-DsRed or FTL-DsRed fusion reporter in infected cells were created, but only the adenovirus expressing FTH-DsRed resulted in a high level of red fluorescence in cells. Delivery and expression of FTH-DsRed in the mouse brain using adenovirus was detected by MRI and fluorescence imaging, revealing a T-2 shortening effect and an increase of contrast in T-2-weighted images at the sites co-localized with strong red fluorescence. While the details of the structure of ferritin-DsRed fusion reporter remains to be solved, this dual reporter is useful for visualizing dynamic processes such as the migration of reporter-transfected stem cells or metastasis of tumors using MRI with the added flexibility of combining optical tools such as fluorescence activated cell sorting and fluorescence microscopy.
    Appears in Collections:[生物科技系(所)] 期刊論文

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