Preliminary investigation on adenovirus-mediated transferrin receptor reporter gene in colorectal cancer cell MR imaging
10.13929/j.1672-8475.201712016
- VernacularTitle:腺病毒介导转铁蛋白受体报告基因在结直肠癌细胞MRI中的初步观察
- Author:
Mengling XU
1
;
Yifan WANG
;
Hua HE
;
Fabao GAO
;
Yulin GUO
Author Information
1. 宁夏医科大学基础医学院
- Keywords:
Receptors,transferrin;
Magnetic resonance imaging;
Rectal neoplasms;
Reporter gene
- From:
Chinese Journal of Interventional Imaging and Therapy
2018;15(5):311-315
- CountryChina
- Language:Chinese
-
Abstract:
Objective To explore the best multiplicities of infection (MOI),the expression of the target gene and in vitro MR imaging of adenovirus vector-mediated transferrin receptor (TFRC) reporter gene transfection of human colorectal cancer Lovo cells.Methods Lovo cells were transfected with recombinant adenovirus (Ad-TFRC) at 5,10,50,100 MOI to determine the best MOI,and quantitative real-time PCR was performed to detect the eDNA of TFRC.The transfected cells were incubated in the culture medium including Tf-USPIO of various concentrations,and were observed by Prussian blue staining,then the cell viability was evaluated via Trypan blue staining.The labeled cells were scanned with 7.0T MR T2W,T2 map,T2* map sequences,and the signal intensities were analyzed.Results Ad-TFRC were successfully transfected into Lovo cells.The best MOI was 50,and the efficiency of infection was more than 90%.The relative expression amount of TFRC in transfected cells was higher than that in control Lovo cells by real-time quantitive PCR (P< 0.01).Prussian blue staining showed numerous blue iron particles in transfected cells when the best labeling concentration was 1.5 μg/ml.Trypan blue staining results of transfected Lovo cells and control Lovo cells was (93.80± 1.60)% and (95.10±2.30) %,respectively (P>0.05).MR imaging in vitro showed that compared with control Lovo cells,the signal intensity decreased on T2WI,T2 map and T2* map sequences in transfected Lovo cells (P<0.05).Conclusion TFRC reporter gene can be efficiently mediated by adenovirus for expression in Lovo cells.After magnetization labeling,7.0T MR imaging of Lovo cells can be successfully achieved in vitro.