波谱学杂志 ›› 2019, Vol. 36 ›› Issue (2): 127-137.doi: 10.11938/cjmr20182659

• 天眷波谱青年论坛特邀稿件 • 上一篇    下一篇

一种示踪干细胞的磁共振-荧光双模成像探针

赵敏敏1,2, 张艳辉2, 张朋利2, 谭波2, 蒋海珍1, 张海禄2, 邓宗武2   

  1. 1. 上海大学 理学院, 上海 200444;
    2. 中国科学院 苏州纳米技术与纳米仿生研究所, 江苏 苏州 215123
  • 收稿日期:2018-06-06 发布日期:2018-07-31
  • 通讯作者: 张海禄 Tel:+86-51-262872713, E-mail:hlzhang2008@sinano.ac.cn;邓宗武 Tel:+86-51-262872559, E-mail:zwdeng2007@sinano.ac.cn E-mail:hlzhang2008@sinano.ac.cn;zwdeng2007@sinano.ac.cn
  • 作者简介:张海禄博士,中国科学院苏州纳米技术与纳米仿生研究所研究员,2008年博士毕业于中国科学院武汉物理与数学研究所.目前任江苏省核磁共振专业委员会副主任委员,中华放射学会磁共振物理与工程学组委员,中国晶体学会药物学专业委员会常务委员.他的研究领域主要为药物固态化学和纳米-生物界面物理.
  • 基金资助:
    the National Natural Science Foundation of China (31371010, 21673281); Funds from Youth Innovation Promotion Association of the Chinese Academy of Sciences (2012242); Key Research Project from the Ministry of Science and Technology of China (2017YFA0104300).

A Magnetic Resonance-Fluorescent Dual-Mode Imaging Probe for Stem Cell Tracking

ZHAO Min-min1,2, ZHANG Yan-hui2, ZHANG Peng-li2, TAN Bo2, JIANG Hai-zhen1, ZHANG Hai-lu2, DENG Zong-wu2   

  1. 1. College of Sciences, Shanghai University, Shanghai 200444, China;
    2. Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, China
  • Received:2018-06-06 Published:2018-07-31
  • Supported by:
    the National Natural Science Foundation of China (31371010, 21673281); Funds from Youth Innovation Promotion Association of the Chinese Academy of Sciences (2012242); Key Research Project from the Ministry of Science and Technology of China (2017YFA0104300).

摘要: 本文设计并合成了Gd基磁共振-荧光双模成像探针——Gd-DOTA-PEG-GA,通过电穿孔的方式标记人源间充质干细胞(hMSCs).电穿孔标记诱导细胞将探针组装成团簇状纳米粒子进入细胞质,显著延长其与细胞结合的时间,并呈现出明显的T2信号减弱效应,且信号减弱效应可以持续7天以上.在水溶液中,该探针的发射带集中在498 nm,并且荧光强度在一周内无明显衰减.该探针标记的细胞在荧光倒置显微镜下呈现绿色荧光.这些结果表明该探针可以作为磁共振-荧光双模成像探针用于干细胞示踪.

关键词: 磁共振成像, 荧光成像, 双模探针, 人源间充质干细胞

Abstract: A magnetic resonance (MR)-fluorescent dual-mode imaging probe was prepared by conjugating guaiazulene to Gd-DOTA, and used to label human mesenchymal stem cells (hMSCs) via electroporation. The probe self-assembled into nanoclusters in the cytoplasm, resulting in a significant reduction in T2-weighted signal intensity that persisted up to 7 days. The fluorescence signal of the probe was observed at 498 nm, and the labelled hMSCs emitted a green fluorescence. The MR-fluorescent dual-mode imaging probe can potentially be used for stem cell tracking in vivo.

Key words: magnetic resonance imaging, fluorescent imaging, dual-mode probe, human mesenchymal stem cell

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