Detection threshold of single SPIO-Labeled cells with FIESTA

被引:184
作者
Heyn, C
Bowen, CV
Rutt, BK
Foster, PJ
机构
[1] John P Robarts Res Inst, Imaging Res Labs, London, ON N6A 5K8, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A1, Canada
关键词
magnetic resonance imaging; iron-oxide; single cell; detection threshold; cell tracking;
D O I
10.1002/mrm.20356
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
MRI of superparamagnetic iron oxide (SPIO)-labeled cells has become a valuable tool for studying the in vivo trafficking of transplanted cells. Cellular detection with MRI is generally considered to be orders of magnitude less sensitive than other techniques, such as positron emission tomography (PET), single photon emission-computed tomography (SPECT), or optical fluorescence microscopy. However, an analytic description of the detection threshold for single SPIO-labeled cells and the parameters that govern detection has not been adequately provided. In the present work, the detection threshold for single SPIO-labeled cells and the effect of resolution and SNR were studied for a balanced steady-state free precession (SSFP) sequence (3D-FIESTA). Based on the results from both theoretical and experimental analyses, an expression that predicts the minimum detectable mass of SPIO (m.) required to detect a single cell against a uniform signal background was derived: m(c) = 5v/(K-fsl (.) SNR), where v is the voxel volume, SNR is the image signal-to-noise ratio, and K-fsl is an empirical constant measured to be 6.2 +/- 0.5 x 10(-5) mu/pgFe. Using this expression, it was shown that the sensitivity of MRI is not very different from that of PET, requiring femtomole quantities of SPIO iron for detection under typical micro-imaging conditions (100 mum isotropic resolution, SNR = 60). The results of this work will aid in the design of cellular imaging experiments by defining the lower limit of SPIO labeling required for single cell detection at any given resolution and SNR. (C) 2005 Wiley-Liss, Inc.
引用
收藏
页码:312 / 320
页数:9
相关论文
共 37 条
[1]   Ex vivo cell labeling with 64Cu-pyruvaldehyde-bis(N4-methylthiosemicarbazone) for imaging cell trafficking in mice with positron-emission tomography [J].
Adonai, N ;
Nguyen, KN ;
Walsh, J ;
Iyer, M ;
Toyokuni, T ;
Phelps, ME ;
McCarthy, T ;
McCarthy, DW ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) :3030-3035
[2]   Receptor-mediated endocytosis of iron-oxide particles provides efficient labeling of dendritic cells for in vivo MR imaging [J].
Ahrens, ET ;
Feili-Hariri, M ;
Xu, H ;
Genove, G ;
Morel, PA .
MAGNETIC RESONANCE IN MEDICINE, 2003, 49 (06) :1006-1013
[3]   Intracytoplasmic tagging of cells with ferumoxides and transfection agent for cellular magnetic reisonance imaging after cell transplantation: Methods and techniques [J].
Arbab, AS ;
Bashaw, LA ;
Miller, BR ;
Jordan, EK ;
Bulte, JWM ;
Frank, JA .
TRANSPLANTATION, 2003, 76 (07) :1123-1130
[4]   Detection of neuritic plaques in Alzheimer's disease by magnetic resonance microscopy [J].
Benveniste, H ;
Einstein, G ;
Kim, KR ;
Hulette, C ;
Johnson, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :14079-14084
[5]  
Botti C, 1997, EUR J NUCL MED, V24, P497
[6]   Application of the static dephasing regime theory to superparamagnetic iron-oxide loaded cells [J].
Bowen, CV ;
Zhang, XW ;
Saab, G ;
Gareau, PJ ;
Rutt, BK .
MAGNETIC RESONANCE IN MEDICINE, 2002, 48 (01) :52-61
[7]   Magnetodendrimers allow endosomal magnetic labeling and in vivo tracking of stem cells [J].
Bulte, JWM ;
Douglas, T ;
Witwer, B ;
Zhang, SC ;
Strable, E ;
Lewis, BK ;
Zywicke, H ;
Miller, B ;
van Gelderen, P ;
Moskowitz, BM ;
Duncan, ID ;
Frank, JA .
NATURE BIOTECHNOLOGY, 2001, 19 (12) :1141-1147
[8]  
Bulte JWM, 1999, MAGN RESON MED, V42, P379, DOI 10.1002/(SICI)1522-2594(199908)42:2<379::AID-MRM20>3.0.CO
[9]  
2-L
[10]   Neurotransplantation of magnetically labeled oligodendrocyte progenitors: Magnetic resonance tracking of cell migration and myelination [J].
Bulte, JWM ;
Zhang, SC ;
van Gelderen, P ;
Herynek, V ;
Jordan, EK ;
Duncan, ID ;
Frank, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :15256-15261