Self-assembling nanocomplexes by combining ferumoxytol, heparin and protamine for cell tracking by magnetic resonance imaging

被引:170
作者
Thu, Mya S. [1 ,2 ]
Bryant, L. Henry [1 ,2 ]
Coppola, Tiziana [1 ,2 ]
Jordan, E. Kay [1 ,2 ]
Budde, Matthew D. [1 ,2 ]
Lewis, Bobbi K. [1 ,2 ]
Chaudhry, Aneeka [1 ,2 ]
Ren, Jiaqiang [3 ]
Varma, Nadimpalli Ravi S. [4 ]
Arbab, Ali S. [4 ]
Frank, Joseph A. [1 ,2 ,5 ]
机构
[1] NIH, Frank Lab, Bethesda, MD 20892 USA
[2] NIH, Lab Diagnost Radiol Res, Dept Radiol & Imaging Sci, Bethesda, MD 20892 USA
[3] NIH, Cell Proc Sect, Dept Transfus Med, Ctr Clin, Bethesda, MD 20892 USA
[4] Henry Ford Hosp, Dept Radiol, Cellular & Mol Imaging Lab, Detroit, MI 48202 USA
[5] NIH, Natl Inst Biomed Imaging & Bioengn, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
STEM-CELLS; DELIVERY-SYSTEM; LABELED CELLS; IRON; NANOPARTICLES; MRI; OPTIMIZATION; FERUMOXIDES; EXPRESSION; DRUGS;
D O I
10.1038/nm.2666
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report on a new straightforward magnetic cell-labeling approach that combines three US Food and Drug Administration (FDA)-approved drugs-ferumoxytol, heparin and protamine-in serum-free medium to form self-assembling nanocomplexes that effectively label cells for in vivo magnetic resonance imaging (MRI). We observed that the ferumoxytol-heparin-protamine (HPF) nanocomplexes were stable in serum-free cell culture medium. HPF nanocomplexes show a threefold increase in T2 relaxivity compared to ferumoxytol. Electron microscopy showed internalized HPF in endosomes, which we confirmed by Prussian blue staining of labeled cells. There was no long-term effect or toxicity on cellular physiology or function of HPF-labeled hematopoietic stem cells, bone marrow stromal cells, neural stem cells or T cells when compared to controls. In vivo MRI detected 1,000 HPF-labeled cells implanted in rat brains. This HPF labeling method should facilitate the monitoring by MRI of infused or implanted cells in clinical trials.
引用
收藏
页码:463 / U165
页数:6
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