Sun Gui-Jun, Qin Xiao-Dong, Wang Shi-Qin, Hu Hui-Zhen, Lu Xiao-Yan, Jin Jia-Jia, Wu Sheng-Rong, He Xiang-Yi
Research Institute 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. 2019 Feb 1;37(1):25-30. doi: 10.7518/hxkq.2019.01.005.
This study aims to establish an effective and stable periodontal ligament cell line stably expressing human telomerase reverse transcriptase (hTERT) gene by using the adenovirus method.
Polymerase chain reaction (PCR) was used to amplify the full length of hTERT gene to construct recombinant adenovirus plasmid pAd-pshuttle-cmv-hTERT. Packaged adenovirus particles were used for infection of human periodontal ligament cells. The expression levels of hTERT and osteogenic genes, such as alkaline phosphatase, Runt-related transcription factor 2, bone sialoprotein, osteocalcin, osteopontin, and collagen Ⅰ mRNA, were detected by quantitative real-time PCR (qRT-PCR). The ability of osteogenic differentiation was observed by alizarin red staining, and the cell proliferation was determined by CCK-8.
Adenovirus particles containing the hTERT gene were successfully constructed and infected with periodontal ligament cells. The infected cells were similar to normal periodontal ligament cells. The qRT-PCR results showed that hTERT and osteogenesis-associated genes were highly expressed in the periodontal ligament cell lines constructed by adenoviruses. Alizarin red staining showed that the periodontal ligament cell line had strong osteogenic differentiation capability. CCK-8 showed that the periodontal ligament cell line had strong proliferation capability.
The human periodontal ligament cell line with high efficiency and stable expression of hTERT was established by the adenovirus method, thereby providing an ideal cell line for studying the mechanism of periodontal regeneration.
本研究旨在通过腺病毒法建立稳定表达人端粒酶逆转录酶(hTERT)基因的有效且稳定的牙周膜细胞系。
采用聚合酶链反应(PCR)扩增hTERT基因全长,构建重组腺病毒质粒pAd-pshuttle-cmv-hTERT。用包装好的腺病毒颗粒感染人牙周膜细胞。通过定量实时PCR(qRT-PCR)检测hTERT及成骨基因如碱性磷酸酶、 runt相关转录因子2、骨唾液蛋白、骨钙素、骨桥蛋白和Ⅰ型胶原mRNA的表达水平。通过茜素红染色观察成骨分化能力,用CCK-8检测细胞增殖情况。
成功构建含hTERT基因的腺病毒颗粒并感染牙周膜细胞。感染后的细胞与正常牙周膜细胞相似。qRT-PCR结果显示,hTERT及成骨相关基因在腺病毒构建的牙周膜细胞系中高表达。茜素红染色显示该牙周膜细胞系具有较强的成骨分化能力。CCK-8检测显示该牙周膜细胞系具有较强的增殖能力。
通过腺病毒法建立了高效稳定表达hTERT的人牙周膜细胞系,为研究牙周再生机制提供了理想的细胞系。