Volume 76, Issue 1, Pages (January 1999)

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Volume 76, Issue 1, Pages 103-109 (January 1999) Detection of Single Mammalian Cells by High-Resolution Magnetic Resonance Imaging  Stephen J. Dodd, Mangay Williams, Joseph P. Suhan, Donald S. Williams, Alan P. Koretsky, Chien Ho  Biophysical Journal  Volume 76, Issue 1, Pages 103-109 (January 1999) DOI: 10.1016/S0006-3495(99)77182-1 Copyright © 1999 The Biophysical Society Terms and Conditions

Figure 1 Representative TEM image showing accumulation of SPIO particles inside the phagocytic vacuoles of T cells. Regions of the cells containing the particles are shown magnified below the main image. Approximately 20% of the T cells were labeled with SPIO particles by endocytosis under our experimental conditions as shown by TEM. That the accumulated particles essentially act as a single larger particle with paramagnetic properties is one of the advantages of cell labeling via endocytosis. Biophysical Journal 1999 76, 103-109DOI: (10.1016/S0006-3495(99)77182-1) Copyright © 1999 The Biophysical Society Terms and Conditions

Figure 2 Gradient-echo images showing SPIO-labeled (A, C, E) and unlabeled (B, D, F) T cell samples. Cell concentrations were as follows: (A) and (B), 2.0×106 T cells/ml; (C) and (D), 1.0×106 T cells/ml; (E) and (F), 0.25×106 T-cells/ml. Imaging parameters were as follows: TR/TE=1000/30ms; FA=45°; matrix size=128×128; FOV=6.4mm; slice thickness=100μm; in-plane resolution=50×50μm; acquisition bandwidth=20kHz; number of averages=8; experiment time=17min. In each case, the direction of the read gradient was from left to right and the phase-encoding direction was vertical. Bulk samples for high-resolution MRI studies were prepared in 1-ml plastic syringes by suspending labeled and unlabeled T cell samples in 3% gelatin. Biophysical Journal 1999 76, 103-109DOI: (10.1016/S0006-3495(99)77182-1) Copyright © 1999 The Biophysical Society Terms and Conditions

Figure 3 Plot showing MR signal intensity decrease due to the presence of SPIO particles as a function of voxel size. Biophysical Journal 1999 76, 103-109DOI: (10.1016/S0006-3495(99)77182-1) Copyright © 1999 The Biophysical Society Terms and Conditions

Figure 4 Plot showing MR signal intensity decrease due to the presence of SPIO particles as a function of echo time (TE). Biophysical Journal 1999 76, 103-109DOI: (10.1016/S0006-3495(99)77182-1) Copyright © 1999 The Biophysical Society Terms and Conditions

Figure 5 (A) MR image of microscope slide containing 10×106 SPIO-labeled T cells/ml in 3% gelatin. (B) MR image of microscope slide containing free SPIO sample (1.0μg Fe/ml) with twice the amount of iron as the previous T cell sample labeled with SPIO particles. Imaging parameters were as follows: Gradient-echo image TR/TE=1000/40ms; FA=45o; acquisition bandwidth=15kHz; NA=32 for the labeled sample and 64 for the unlabeled sample; imaging time=2h for the labeled sample and 4h for the free SPIO sample. Biophysical Journal 1999 76, 103-109DOI: (10.1016/S0006-3495(99)77182-1) Copyright © 1999 The Biophysical Society Terms and Conditions

Figure 6 MR image of a microscope slide containing T cells colabeled with SPIO and DiI (A), fluorescence image of the same microscope slide (B), and a comparison of the two images (C). Biophysical Journal 1999 76, 103-109DOI: (10.1016/S0006-3495(99)77182-1) Copyright © 1999 The Biophysical Society Terms and Conditions