In Vivo Targeted Magnetic Resonance Imaging of Endogenous Neural Stem Cells in the Adult Rodent Brain

被引:4
|
作者
Zhong, Xiao-Mei [1 ]
Zhang, Fang [1 ]
Yang, Ming [2 ]
Wen, Xue-Hua [1 ]
Zhang, Xiang [1 ]
Duan, Xiao-Hui [1 ]
Shen, Jun [1 ]
机构
[1] Sun Yat Sen Univ, Dept Radiol, Sun Yat Sen Mem Hosp, Guangzhou 510120, Guangdong, Peoples R China
[2] Southeast Univ, Dept Radiol, Zhongda Hosp, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
SUBVENTRICULAR ZONE; PROGENITOR CELLS; MIGRATION; MRI; PROLIFERATION; NEUROGENESIS; PRECURSORS; UPDATE;
D O I
10.1155/2015/131054
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Neural stem cells in the adult mammalian brain have a significant level of neurogenesis plasticity. In vivo monitoring of adult endogenous NSCs would be of great benefit to the understanding of the neurogenesis plasticity under normal and pathological conditions. Here we show the feasibility of in vivo targeted MR imaging of endogenous NSCs in adult mouse brain by intraventricular delivery of monoclonal anti-CD15 antibody conjugated superparamagnetic iron oxide nanoparticles. After intraventricular administration of these nanoparticles, the subpopulation of NSCs in the anterior subventricular zone and the beginning of the rostral migratory stream could be in situ labeled and were in vivo visualized with 7.0-T MR imaging during a period from 1 day to 7 days after the injection. Histology confirmed that the injected targeted nanoparticles were specifically bound to CD15 positive cells and their surrounding extracellular matrix. Our results suggest that in vivo targeted MR imaging of endogenous neural stem cells in adult rodent brain could be achieved by using anti-CD15-SPIONs as the molecular probe; and this targeting imaging strategy has the advantage of a rapid in vivo monitoring of the subpopulation of endogenous NSCs in adult brains.
引用
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页数:11
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