A primer on in vivo cell tracking using MRI

被引:5
|
作者
Cheng, Hai-Ling Margaret [1 ,2 ,3 ]
机构
[1] Univ Toronto, Inst Biomed Engn, Toronto, ON, Canada
[2] Univ Toronto, Edward S Rogers Sr Dept Elect & Comp Engn, Toronto, ON, Canada
[3] Ted Rogers Ctr Heart Res, Translat Biol & Engn Program, Toronto, ON, Canada
基金
加拿大健康研究院; 加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
cellular imaging and cell tracking; manganese; iron oxide; gadolinium; reporter gene; ferritin; DIVALENT METAL TRANSPORTER; MANGANESE-ENHANCED MRI; MESENCHYMAL STEM-CELLS; CONTRAST AGENT; F-19; MRI; REPORTER GENE; BRAIN-TUMORS; FERRITIN OVEREXPRESSION; TRANSPLANTED CELLS; IMAGING TRACKING;
D O I
10.3389/fmed.2023.1193459
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cell tracking by in vivo magnetic resonance imaging (MRI) offers a collection of multiple advantages over other imaging modalities, including high spatial resolution, unlimited depth penetration, 3D visualization, lack of ionizing radiation, and the potential for long-term cell monitoring. Three decades of innovation in both contrast agent chemistry and imaging physics have built an expansive array of probes and methods to track cells non-invasively across a diverse range of applications. In this review, we describe both established and emerging MRI cell tracking approaches and the variety of mechanisms available for contrast generation. Emphasis is given to the advantages, practical limitations, and persistent challenges of each approach, incorporating quantitative comparisons where possible. Toward the end of this review, we take a deeper dive into three key application areas - tracking cancer metastasis, immunotherapy for cancer, and stem cell regeneration - and discuss the cell tracking techniques most suitable to each.
引用
收藏
页数:16
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