MRI detection of single particles for cellular imaging

被引:387
作者
Shapiro, EM
Skrtic, S
Sharer, K
Hill, JM
Dunbar, CE
Koretsky, AP
机构
[1] NINDS, Lab Funct & Mol Imaging, NIH, Bethesda, MD 20892 USA
[2] NHLBI, Hematol Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1073/pnas.0403918101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is rapid growth in the use of MRI for molecular and cellular imaging. Much of this work relies on the high relaxivity of nanometer-sized, ultrasmall dextran-coated iron oxide particles. Typically, millions of dextran-coated ultrasmall iron oxide particles must be loaded into cells for efficient detection. Here we show that single, micrometer-sized iron oxide particles (MPIOs) can be detected by MRI in vitro in agarose samples, in cultured cells, and in mouse embryos. Experiments studying effects of MRI resolution and particle size from 0.76 to 1.63 mum indicated that T-2(*) effects can be readily detected from single MPIOs at 50-mum resolution and significant signal effects could be detected at resolutions as low as 200 mum. Cultured cells were labeled with fluorescent MPIOs such that single particles were present in individual cells. These single particles in single cells could be detected both by MRI and fluorescence microscopy. Finally, single particles injected into single-cell-stage mouse embryos could be detected at embryonic day 11.5, demonstrating that even after many cell divisions, daughter cells still carry individual particles. These results demonstrate that MRI can detect single particles and indicate that single-particle detection will be useful for cellular imaging.
引用
收藏
页码:10901 / 10906
页数:6
相关论文
共 36 条
[11]  
Dousset V, 1999, MAGNET RESON MED, V41, P329, DOI 10.1002/(SICI)1522-2594(199902)41:2<329::AID-MRM17>3.0.CO
[12]  
2-Z
[13]   Imaging single mammalian cells with a 1.5 T clinical MRI scanner [J].
Foster-Gareau, P ;
Heyn, C ;
Alejski, A ;
Rutt, BK .
MAGNETIC RESONANCE IN MEDICINE, 2003, 49 (05) :968-971
[14]   Magnetic intracellular labeling of mammalian cells by combining (FDA-approved) superparamagnetic iron oxide MR contrast agents and commonly used transfection agents [J].
Frank, JA ;
Zywicke, H ;
Jordan, EK ;
Mitchell, J ;
Lewis, BK ;
Miller, B ;
Bryant, LH ;
Bulte, JWM .
ACADEMIC RADIOLOGY, 2002, 9 :S484-S487
[15]  
Gupta H, 1996, Magn Reson Imaging Clin N Am, V4, P171
[16]   Serial cardiac magnetic resonance imaging of injected mesenchymal stem cells [J].
Hill, JM ;
Dick, AJ ;
Raman, VK ;
Thompson, RB ;
Yu, ZX ;
Hinds, KA ;
Pessanha, BSS ;
Guttman, MA ;
Varney, TR ;
Martin, BJ ;
Dunbar, CE ;
McVeigh, ER ;
Lederman, RJ .
CIRCULATION, 2003, 108 (08) :1009-1014
[17]   Highly efficient endosomal labeling of progenitor and stem cells with large magnetic particles allows magnetic resonance imaging of single cells [J].
Hinds, KA ;
Hill, JM ;
Shapiro, EM ;
Laukkanen, MO ;
Silva, AC ;
Combs, CA ;
Varney, TR ;
Balaban, RS ;
Koretsky, AP ;
Dunbar, CE .
BLOOD, 2003, 102 (03) :867-872
[18]   Monitoring of implanted stem cell migration in vivo:: A highly resolved in vivo magnetic resonance imaging investigation of experimental stroke in rat [J].
Hoehn, M ;
Küstermann, E ;
Blunk, J ;
Wiedermann, D ;
Trapp, T ;
Wecker, S ;
Föcking, M ;
Arnold, H ;
Hescheler, J ;
Fleischmann, BK ;
Schwindt, W ;
Bührle, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (25) :16267-16272
[19]   High-efficiency intracellular magnetic labeling with novel superparamagnetic-tat peptide conjugates [J].
Josephson, L ;
Tung, CH ;
Moore, A ;
Weissleder, R .
BIOCONJUGATE CHEMISTRY, 1999, 10 (02) :186-191
[20]   Macrophage accumulation associated with rat cardiac allograft rejection detected by magnetic resonance imaging with ultrasmall superparamagnetic iron oxide particles [J].
Kanno, S ;
Wu, YJL ;
Lee, PC ;
Dodd, SJ ;
Williams, M ;
Griffith, BP ;
Ho, C .
CIRCULATION, 2001, 104 (08) :934-938