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MRI Detection of Single Particles for Cellular Imaging
Erik M. Shapiro, Stanko Skrtic, Kathryn Sharer, Jonathan M. Hill, Cynthia E. Dunbar, Alan P. Koretsky and Mildred Cohn
Proceedings of the National Academy of Sciences of the United States of America
Vol. 101, No. 30 (Jul. 27, 2004), pp. 10901-10906
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/3372825
Page Count: 6
You can always find the topics here!Topics: Radiation counters, Embryos, Imaging, Signals, Iron oxides, Hepatocytes, Daughter cells, Cultured cells, Stem cells, Fluorescence
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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 μm indicated that T2 * effects can be readily detected from single MPIOs at 50-μm resolution and significant signal effects could be detected at resolutions as low as 200 μm. 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.
Proceedings of the National Academy of Sciences of the United States of America © 2004 National Academy of Sciences