Dai Hai-Yang, He Rong, Zhang Ying, Wu Ren-Hua, Xiao Ye-Yu
Department of Medical Imaging, Huizhou Municipal Central Hospital, Huizhou, China.
Department of Medical Imaging, the 2nd Affiliated Hospital of Shantou University Medical College, Shantou, China.
PLoS One. 2017 Sep 25;12(9):e0185260. doi: 10.1371/journal.pone.0185260. eCollection 2017.
The aim of the present work was to verify whether adenoviral vector mediated ferritin over-expression in mesenchymal stem cells could be detected by 7T MRI device, and to explore the relationship between ferritin content and MRI signal intensities.
A recombined adenoviral vector (rAdV) encoding ferritin heavy chain (FTH1) subunit was specially designed for the aim of infecting bone marrow mesenchymal stem cells (BMSCs). Ferritin over-expression in BMSCs was determined by cell immunocytochemistry and the ferritin content in cells was determined by ELISA assay. BMSCs were subjected to cell viability, proliferation and multi-differentiation analyses as well as 7T MRI test using fast spin-echo pulse sequence. The R2 value andδR2 were calculated according to T2 mapping images.
As was confirmed by cell immunocytochemistry and ELISA assay, rAdV mediated ferritin was over-expressed in BMSCs. Ferritin over-expression did not interfere with stem cell viability or pluripotent differentiation but slowed cell proliferation. The R2 value of BMSCs-FTH1 vs control BMSCs from 1-4 weeks was16.65±1.28 s-1 vs 13.99±0.80 s-1, (t = 3.94, p = 0.004), 15.63±1.37 s-1 vs 13.87±0.83 s-1 (t = 2.47, p = 0.039), 15.53±0.88 s-1 vs 14.25±0.53 s-1 (t = 2.80, p = 0.023) and 14.61±1.28 s-1 vs 13.69±1.03 s-1 (t = 1.25, p = 0.24), respectively. δR2 gradually decreased from 1-4 weeks and the difference between the groups had statistical significance (F = 12.45, p<0.01).δR2 was positively correlated with OD value (r = 0.876, p<0.01) and ferritin concentration (r = 0.899, p<0.01) as determined by Pearson correlation.
Our study confirms that ferritin could be over-expressed in BMSCs as a result of rAdV mediated infection and could be quantitatively detected by 7T MRI device. The differences in T2 signal intensities and R2 values stem from internal contrast generated by endogenous ferritin over-expression. The correlation between δR2, OD and ferritin concentration suggests that MRI can detect ferritin signal change accurately.
本研究旨在验证7T磁共振成像(MRI)设备能否检测到腺病毒载体介导的间充质干细胞中铁蛋白的过表达,并探讨铁蛋白含量与MRI信号强度之间的关系。
专门设计一种编码铁蛋白重链(FTH1)亚基的重组腺病毒载体(rAdV),用于感染骨髓间充质干细胞(BMSCs)。通过细胞免疫细胞化学法测定BMSCs中铁蛋白的过表达情况,采用酶联免疫吸附测定(ELISA)法测定细胞中铁蛋白含量。对BMSCs进行细胞活力、增殖和多向分化分析,并使用快速自旋回波脉冲序列进行7T MRI检测。根据T2映射图像计算R2值和δR2值。
细胞免疫细胞化学和ELISA检测证实,rAdV介导的铁蛋白在BMSCs中过表达。铁蛋白过表达不影响干细胞活力或多能分化,但减缓细胞增殖。1 - 4周时,BMSCs - FTH1组与对照BMSCs组的R2值分别为16.65±1.28 s-1对13.99±0.80 s-1,(t = 3.94,p = 0.004);15.63±1.37 s-1对13.87±0.83 s-1(t = 2.47,p = 0.039);15.53±0.88 s-1对14.25±0.53 s-1(t = 2.80,p = 0.023);14.61±1.28 s-1对13.69±1.03 s-1(t = 1.25,p = 0.24)。δR2在1 - 4周逐渐降低,组间差异具有统计学意义(F = 12.45,p<0.01)。Pearson相关性分析显示,δR2与OD值(r = 0.876,p<0.01)和铁蛋白浓度(r = 0.899,p<0.01)呈正相关。
我们的研究证实,rAdV介导的感染可使BMSCs中铁蛋白过表达,且7T MRI设备可对其进行定量检测。T2信号强度和R2值的差异源于内源性铁蛋白过表达产生的内在对比。δR2、OD与铁蛋白浓度之间的相关性表明,MRI能够准确检测铁蛋白信号变化。