Quantitative imaging of Na/I symporter transgene expression using positron emission tomography in the living animal

被引:74
作者
Groot-Wassink, T
Aboagye, EO
Wang, YH
Lemoine, NR
Reader, AJ
Vassaux, G [1 ]
机构
[1] Canc Res UK Mol Oncol Unit, London W12 0NN, England
[2] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dept Canc Med, PET Oncol Grp, London W12 0NN, England
[3] UMIST, Dept Instrumentat & Analyt Sci, Manchester M60 1QD, Lancs, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1016/j.ymthe.2003.12.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Transgene expression can be measured in living animals by positron emission tomography (PET) using reporter genes associated with radiolabeled substrates or ligands. We examined here whether PET images obtained with a new reporter gene system (sodium/iodide symporter (NIS) and [I-124] iodide) could provide quantitative information on gene expression in mice. Mice received various doses of recombinant adenovirus in which the expression of the NIS cDNA was driven by the CMV promoter and subsequently [I-124]iodide. Postmortem gamma counting of liver biopsies was correlated to the adenovirus dose and with NIS mRNA concentration. In addition, immunohistochemically NIS-positive cells increased with higher tissue activities. Finally, a linear relationship existed between the postmortem gamma counting in liver tissues and that calculated from images obtained through small animal PET scanning (r = 0.9581), although there was a bias at high and low specific values. This systematic study on 35 animals demonstrates that quantitative information on gene expression can be obtained from PET images using the NIS reporter system. This new methodology of quantitative imaging of gene expression presents the advantage of avoiding extensive radiochemistry, an important step for more disseminated use of this emerging technology. In addition, this work supports further development of the NIS system for noninvasive assessment of gene delivery in preclinical and clinical studies.
引用
收藏
页码:436 / 442
页数:7
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