Effective tracking of bone mesenchymal stem cells in vivo by magnetic resonance imaging using melanin-based gadolinium3+ nanoparticles

被引:23
作者
Cai, Wen-Wen [1 ]
Wang, Ling-Jie [1 ]
Li, Si-Jin [2 ]
Zhang, Xi-Ping [3 ]
Li, Ting-Ting- [2 ]
Wang, Ying-Hua [1 ]
Yang, Xi [1 ]
Xie, Jun [1 ]
Li, Jian-Ding [1 ]
Liu, Shi-Jie [1 ]
Xu, Wen [1 ]
He, Sheng [1 ]
Cheng, Zhen [4 ]
Fan, Qu-Li [5 ,6 ]
Zhang, Rui-Ping [1 ]
机构
[1] Shanxi Med Univ, Clin Med Coll 1, Dept Med Imaging, Taiyuan 030001, Shanxi Province, Peoples R China
[2] Shanxi Med Univ, Mol Imaging Precis Med Collaborat Innovat Ctr, Taiyuan 030001, Shanxi Province, Peoples R China
[3] Zhejiang Canc Hosp, Dept Tumor Surg, Hangzhou 310022, Zhejiang, Peoples R China
[4] Stanford Univ, Mol Imaging Program Stanford, Stanford, CA 94305 USA
[5] Nanjing Univ Posts & Telecommun, Key Lab Organ Elect & Informat Displays, Nanjing 210023, Jiangsu, Peoples R China
[6] Nanjing Univ Posts & Telecommun, Inst Adv Mat, Nanjing 210023, Jiangsu, Peoples R China
关键词
melanin; gadolinium; magnetic resonance imaging; mesenchymal stem cells; tracking; CONTRAST AGENT; STROMAL CELLS; CLINICAL-APPLICATIONS; DELIVERY; THERAPY; MIGRATION; PLATFORM; DISEASE; VITRO; DOTS;
D O I
10.1002/jbm.a.35891
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Tracking transplanted stem cells is necessary to clarify cellular properties and improve transplantation success. In this study, we designed and synthesized melanin-based gadolinium(3+) (Gd3+)-chelate nanoparticles (MNP-Gd3+) of approximate to 7 nm for stem cell tracking in vivo. MNP-Gd3+ possesses many beneficial properties, such as its high stability and sensitivity, shorter T1 relaxation time, higher cell labeling efficiency, and lower cytotoxicity compared with commercial imaging agents. We found that the T1 relaxivity (r(1)) of MNP-Gd3+ was significantly higher than that of Gd-DTPA; the nanoparticles were taken up by bone mesenchymal stem cells (BMSCs) via endocytosis and were broadly distributed in the cytoplasm. Based on an in vitro MTT assay, no cytotoxicity of labeled stem cells was observed for MNP-Gd3+ concentrations of less than 800 mu g/mL. Furthermore, we tracked MNP-Gd3+-labeled BMSCs in vivo using 3.0T MRI equipment. After intramuscular injection, MNP-Gd3+-labeled BMSCs were detected, even after four weeks, by 3T MRI. We concluded that MNP-Gd3+ nanoparticles at appropriate concentrations can be used to effectively monitor and track BMSCs in vivo. MNP-Gd3+ nanoparticles have potential as a new positive MRI contrast agent in clinical applications. (c) 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 131-137, 2017.
引用
收藏
页码:131 / 137
页数:7
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