Sa Zeng, Xiaodong Qin, Xiangyi He, Chunxiao Che, Xiao Zhang, Siyu Xie, Guijun Sun, Lihe Wang
School of Stomatology, Lanzhou University, Lanzhou 730000, China.
Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730000, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2016 Oct 1;34(5):443-447. doi: 10.7518/hxkq.2016.05.002.
To construct a cell line of oral mucosa epithelial cells that stably express human telomerase reverse transcriptase (hTERT) by lentiviral vectors, approaches for the establishment of stable and efficient immortalized oral mucosa epithelial cell lines were explored.
Whole RNA was extracted from 293T cells. The hTERT gene was amplified by polymerase chain reaction (PCR) and cloned into the lentiviral vector as pLVX-puro-hTERT. The lentivirus particles were successfully packaged and used to infect primary oral epithelial cells. The positive cell clones were selected by puromycin. Finally, the expression of hTERT was examined by real-time fluorescent quantitative PCR (qRT-PCR) and Western blot analysis.
The sequencing results confirmed the construction of the recombinant lentivirus pLVX-puro-hTERT. The morphology of infected cells was similar to that of normal oral mucosal epithelial cells, with a cobble stone-like appearance. The qRT-PCR and Western blot results showed that hTERT was overexpressed in infected cells compared with the normal group (P<0.05).
The oral epithelial cell line with stable expression of hTERT was successfully established by the lentivirus, which provides an experimental basis for the establishment of a highly efficient and stable oral epithelial immortalized cell line.
通过慢病毒载体构建稳定表达人端粒酶逆转录酶(hTERT)的口腔黏膜上皮细胞系,探索建立稳定高效的永生化口腔黏膜上皮细胞系的方法。
从293T细胞中提取总RNA。通过聚合酶链反应(PCR)扩增hTERT基因,并将其克隆到慢病毒载体中构建成pLVX-puro-hTERT。成功包装慢病毒颗粒并用于感染原代口腔上皮细胞。用嘌呤霉素筛选阳性细胞克隆。最后,通过实时荧光定量PCR(qRT-PCR)和蛋白质免疫印迹分析检测hTERT的表达。
测序结果证实重组慢病毒pLVX-puro-hTERT构建成功。感染细胞的形态与正常口腔黏膜上皮细胞相似,呈鹅卵石样外观。qRT-PCR和蛋白质免疫印迹结果显示,与正常组相比,感染细胞中hTERT表达上调(P<0.05)。
利用慢病毒成功构建了稳定表达hTERT的口腔上皮细胞系,为建立高效稳定的口腔上皮永生化细胞系提供了实验依据。