lacZ as a Genetic Reporter for Real-Time MRI

被引:33
作者
Bengtsson, Niclas E. [1 ]
Brown, Gary [1 ]
Scott, Edward W. [1 ]
Walter, Glenn A. [1 ]
机构
[1] Univ Florida, Dept Physiol & Funct Gen, Program Stem Cell Biol & Regenerat Med, Gainesville, FL 32610 USA
关键词
MRI; gene reporter; S-Gal; T-2*; relaxometry; iron; HEMATOPOIETIC PROGENITOR CELLS; MESENCHYMAL STEM-CELLS; IN-VIVO DETECTION; CONTRAST AGENTS; MAGNETIC NANOPARTICLES; MOUSE MODEL; IRON; EXPRESSION; FERRITIN; TRANSPLANTATION;
D O I
10.1002/mrm.22235
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
100231 [临床病理学]; 100902 [航空航天医学];
摘要
Molecular imaging based on MRI is currently hampered by the lack of genetic reporters for in vivo imaging. We determined that the commercially available substrate S-Gal (TM) can be used to detect genetically engineered P-galactosidase expressing cells by MRI. The effect and specificity of the reaction between beta-galactosidase and S-Gal (TM) on MRI contrast were determined both in vitro and in vivo. a-galactosidase activity in the presence of S-Gal (TM) resulted in enhanced T-2 and T-2* MR-contrast, which was amplified with increasing magnetic field strengths (4.7-17.6 T) in phantom studies. Using both lacZ(+) transgenic animals and lacZ(+) tissue transplants, we were able to detect labeled cells in live animals in real time. Similar to phantom studies, detection of the labeled cells/tissues in vivo was enhanced at high magnetic fields. These results demonstrate that the genetic reporter, lacZ, can be used as an in vivo marker gene using high-field-strength MRI. Magn Reson Med 63:745-753, 2010. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:745 / 753
页数:9
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