Comparison of Cerenkov Luminescence Imaging (CLI) and gamma camera imaging for visualization of let-7 expression in lung adenocarcinoma A549 Cells

被引:35
作者
Yang, Weidong [1 ]
Qin, Weiwei [2 ]
Hu, Zhenhua [3 ]
Suo, Yaoyu [1 ]
Zhao, Rong [1 ]
Ma, Xiaowei [1 ]
Ma, Wenhui [2 ]
Wang, Tao [4 ]
Liang, Jimin [3 ]
Tian, Jie [5 ]
Wang, Jing [1 ]
机构
[1] Fourth Mil Med Univ, Dept Nucl Med, Xijing Hosp, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Dept Hematol, Tangdu Hosp, Xian 710038, Shaanxi, Peoples R China
[3] Xidian Univ, Life Sci Res Ctr, Sch Life Sci & Technol, Xian 710071, Shaanxi, Peoples R China
[4] Fourth Mil Med Univ, State Key Lab Canc Biol, Dept Biochem, Xian 710032, Shaanxi, Peoples R China
[5] Chinese Acad Sci, Inst Automat, Beijing 100190, Peoples R China
基金
国家自然科学基金重大项目; 中国国家自然科学基金;
关键词
miRNA; Cerenkov luminescence imaging (CLI); Gamma camera imaging; Human sodium/iodine symporter (hNIS); Let-7; TRANSGENE EXPRESSION; ENDOGENOUS MICRORNA; GENE; PROLIFERATION; BIOGENESIS; PROGNOSIS; SIGNATURE; ONCOGENES; INVASION;
D O I
10.1016/j.nucmedbio.2012.05.004
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
Background and Aim: miRNA is an important factor for tumorigenesis which could act as a potential molecular target for tumor diagnosis. The goal of this study was to explore a new method for visualizing the expression of let-7 in lung adenocarcinoma A549 cells by Cerenkov luminescence imaging (CLI) and gamma camera imaging. Methods: The human sodium/iodine symporter (hNIS) and 3'-UTR sequence of the ras gene (RU) that complementarily binds to let-7 were cloned with hNIS serving as the reporter gene. The expression of hNIS regulated by let-7 in the fusion gene hNIS-RU was constructed; the let-7 primer (pri-let-7), which could specifically bind to RU and the mir-143 primer (pri-mir143) not binding with RU, was cloned. A549 cells were transfected with hNIS or hNIS-RU, and additional cells were cotransfected with hNIS-RU and different concentrations of pri-let-7 or pri-mir143. The cells were incubated with 740 kBq I-131-containing media for 1 h, 24 h after transfection. CLI, gamma camera imaging, and gamma counting were subsequently conducted, and the correlation among CLI, gamma camera imaging, and gamma counting was compared when cotransfected with pri-let-7. Results: CLI, gamma camera imaging, and radioactive counting showed that hNIS-transfected A549 cells had significantly higher uptake of I-131 compared to non-transfected cells. The uptake of I-131 in hNIS-RU transfected A549 cells decreased to approximately 70% compared to hNIS-transfected cells, since hNIS-RU expression was suppressed by intracellular let-7. After cotransfection with hNIS-RU and various concentrations of pri-let-7, I-131 uptake gradually decreased with increasing pri-let-7, while I-131 uptake remained roughly unchanged in the presence of hNIS-RU cotransfected with different amounts of pri-mir143. CLI was highly correlated with gamma camera imaging (r(2) = 0.9893) and radioactivity counting (0.9779). Conclusions: Based upon miRNA-regulated reporter genes which mediate the uptake of the radionuclide, both CLI and gamma camera imaging can noninvasively detect miRNA expression in cells, which may provide a new way for the visualization of miRNA expression. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:948 / 953
页数:6
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