Visual recognition and efficient isolation of apoptotic cells with a fluorescent-magnetic-biotargeting multifunctional nanospheres

被引:67
作者
Song, Er-Qun
Wang, Guo-Ping
Xie, Hai-Yan
Zhang, Zhi-Ling
Hu, Jun
Peng, Jun
Wu, Dao-Cheng
Shi, Yun-Bo
Pang, Dai-Wen [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[2] Wuhan Univ, State Key Lab Virol, Wuhan 430072, Peoples R China
[3] Beijing Inst Technol, Sch Life Sci & Technol, Beijing 100081, Peoples R China
[4] Xian Jiaotong Univ, Sch Life Sci & Technol, Xian 710049, Peoples R China
[5] NICHHD, Sect Mol Morphogenesis, Program Cell Regulat & Metab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1373/clinchem.2007.092023
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 [基础医学];
摘要
Background: Fluorescent-magnetic-biotargeting multifunctional nanospheres are likely to find important applications in bioanalysis, biomedicine, and clinical diagnosis. We have been developing such multifunctional nanospheres for biomedical applications. Methods: We covalently coupled avidin onto the surfaces of fluorescent-magnetic bifunctional nanospheres to construct fluorescent-magnetic-biotargeting trifunctional nanospheres and analyzed the functionality and specificity of these trifunctional nanospheres for their ability to recognize and isolate apoptotic cells labeled with biotinylated annexin V, which recognizes phosphatidylserine exposed on the surfaces of apoptotic cells. Results: The multifunctional nanospheres can be used in combination with propidium iodide staining of nuclear DNA to identify cells at different phases of the apoptotic process. Furthermore, we demonstrate that apoptotic cells induced by exposure to ultraviolet light can be isolated simply with a magnet from living cells at an efficiency of at least 80%; these cells can then be easily visualized with a fluorescence microscope. Conclusions: Our results show that fluorescent-magnetic-biotargeting trifunctional nanospheres can be a powerful tool for rapidly recognizing, magnetically enriching and sorting, and simultaneously identifying different kinds of cells. (C) 2007 American Association for Clinical Chemistry.
引用
收藏
页码:2177 / 2185
页数:9
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