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Effect of Telomerase Reverse Transcriptase Gene (TERT) Modification on Proliferation of Mongolian Sheep (Ovis aries) Oviduct Epithelial Cells In vitro |
LIU Yang1,2, HAI Le-Si1,2, LIU Yong-Bin3, LIU Chun-Xia1,2, CAO Jun-Wei1,2,*, ZHANG Yan-Ru1,2,* |
1 College of Life Sciences, Inner Mongolia Agricultural University, Hohhot 010018, China; 2 Inner Mongolia Autonomous Region Key Laboratory of Biomanufacturing, Hohhot 010018, China; 3 Inner Mongolia Academy of Agriculture and Animal Husbandry Sciences, Hohhot 010031, China |
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Abstract Oviduct epithelial cells (OECs) can provide an ideal physiological and biochemical environment to support embryonic development, but their proliferation ability in vitro is weak, which can not meet the needs of experimental research and application. In this study, exogenous telomerase reverse transcriptase gene (TERT) was transferred into Mongolian sheep (Ovis aries) oviduct epithelial cells (sheep OCEs, SOECs), and the proliferation ability of Mongolian sheep oviduct epithelial cells modified by telomerase gene was observed in vitro. Firstly, the SOECs system was established by enzyme digestion, and the recombinant plasmid pCI-neo-TERT was transfected into the primary SOECs by liposome method. The results showed that the expression of TERT gene was detected by qPCR; The growth curve and activity of cytokeratin18 (CK18), a specific marker of epithelial cells, were detected by immunofluorescence. The results showed that TERT gene was successfully introduced into SOECs, and PCR showed that 276 bp TERT gene fragment was expressed in the cells, and the expression of TERT gene was significantly higher than that of the uninfected and transfected pCI-neo empty vector (P<0.001). The transfected cells still retained the biological characteristics of SOECs. The doubling time of P5 TERT-SOECs was 46.61 h, while that of P5 SOECs was 65.03 h. It was obvious that the proliferation rate of TERT-SOECs was significantly higher than that of SOECs. In conclusion, the study successfully established the TERT-SOECs system with strong in vitro proliferation ability, which laid an important foundation for the seed cell supply of germplasm cell bank.
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Received: 05 July 2021
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Corresponding Authors:
*caojunwei1970@163.com; yanru1964@163.com
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[1] 巴雅斯古楞, 冯书堂, 牟玉莲等. 2005. 阳性脂质体介导的转染法的研究[J]. 中国畜牧兽医, 32(11): 33-35. (Ba Y S G L, Feng S T, Mou Y Let al.2005. Study on positive liposome mediated transfection[J]. China Animal Husbandry and Veterinary, 32(11): 33-35.) [2] 付改玲. 2011. 性激素对奶牛输卵管上皮细胞前列腺素受体表达的调控作用[D]. 硕士学位论文,内蒙古农业大学, 导师: 曹金山, pp. 7-8. (Fu G L.2011. The regulation of sex hormone on the expression of prostaglandin receptor in bovine oviduct epithelial cells[D]. Thesis for M.S., Inner Mongolia Agricultural University, Supervisor: Cao J S, pp. 7-8.) [3] 高甜. 2018. 雌激素调控输卵管上皮胃饥饿素基因表达信号通路研究[D]. 硕士学位论文, 内蒙古农业大学, 导师: 曹贵方, 常福厚, pp. 26-27. (Gao T.2018. Study on the signal pathway of estrogen regulating ghrelin gene expression in oviduct epithelium[D]. Thesis for M. S., Inner Mongolia Agricultural University, Supervisor: Cao G F, Chang F H, pp. 26-27.) [4] 郭文文. 2019. 奶牛子宫内膜永生化细胞系的建立[D]. 硕士学位论文, 西北农林科技大学, 导师: 靳亚平, pp. 24-25. (Guo W W.2019. Establishment of immortalized cell line of cow endometrium[D]. Thesis for M.S., Northwest A&F University, Supervisor: Jin Y P, pp. 24-25.) [5] 李秀男. 2018. E_2促进输卵管上皮细胞β-防御素1表达通路及转录组学分析[D]. 硕士学位论文, 内蒙古农业大学, 导师: 曹贵方, pp. 11-12. (Li X N.2018. E_2 promote the growth of oviduct epithelial cells β- defensin-1 expression pathway and transcriptome analysis[D]. Thesis for M.S., Inner Mongolia Agricultural University, Supervisor: Cao G F, pp. 11-12.) [6] 陆笑颜. 2019. 过表达hTERT对人口腔黏膜上皮细胞凋亡通路的影响及机制研究[D]. 博士学位论文, 兰州大学, 导师: 何祥一, 张志东, pp. 44-45. (Lu X Y.2019. Effect of overexpression of hTERT on apoptosis pathway of human oral mucosal epithelial cells and its mechanism [D]. Thesis for Ph. D., Lanzhou University, Supervisor: He X Y, Zhang Z D, pp. 44-45.) [7] 罗荣松. 2020. 奶绵羊与蒙古羊全基因组选择信号和DNA甲基化差异研究[D]. 博士学位论文, 内蒙古大学, 导师: 李光鹏, 姜雨, pp. 3-4. (Luo R S.2020. Study on the difference of whole genome selection signal and DNA methylation between dairy sheep and mongolian sheep [ D]. Thesis for Ph. D., Inner Mongolia University, Supervisor: Li G P, Jiang Y, pp. 3-4.) [8] 尚颖, 赵丽丽, 席雯等. 2018. 成人真皮成纤维细胞原代培养及鉴定[J]. 细胞与分子免疫学杂志, 34(09): 824-828. (Shang Y, Zhao L L, Xi Wet al.2018. Primary culture and identification of adult dermal fibroblasts[J]. Journal of Cell and Molecular Immunology, 34(09): 824-828.) [9] 宋慧子. 2019. 永生化绵羊附睾上皮细胞系的建立及其生物学特性分析[D]. 硕士学位论文, 内蒙古农业大学, 导师: 张家新, pp. 21-22. ( Song H Z.2019. Establishment of immortalized sheep epididymal epithelial cell line and analysis of its biological characteristics[D]. Thesis for M.S., Inner Mongolia Agricultural University, Supervisor: Zhang J X, pp. 21-22.) [10] 孙永刚, 徐惊涛, 才让东智等. 2013. 牦牛输卵管上皮细胞分离培养和纯化鉴定[J]. 生物学杂志, 30(06) : 22-25. (Sun Y G, Xu J T, Cai R D Z, et al.2013. Isolation, culture, purification and identification of yak oviduct epithelial cells[J] . Journal of Biology, 30(06): 22-25.) [11] 谭秀文, 马所峰, 刘新勇等. 2006. 不同物种输卵管上皮细胞培养、纯度检测及支持小鼠胚胎发育的能力[J]. 畜牧兽医学报, 37(9): 878-882. (Tan X W, Ma S F, Liu X Yet al.2006. Culture and purity detection of oviduct epithelial cells from different species and their ability to support mouse embryonic development[J]. Acta Zoologica Veterinary Sinica, 37(9): 878-882.) [12] 王曼曼. 2019. 家兔永生化黑色素细胞的建立、鉴定及应用[D]. 硕士学位论文, 扬州大学, 导师: 吴信生, 潘雨来, pp. 19-20. ( Wang M M.2019. Establishment, identification and application of rabbit immortalized melanocytes [D]. Thesis for M.S., Yangzhou University, Supervisor: Wu X S, Pan Y L, pp. 19-20.) [13] 吴萌, 殷建忠, 朱武洋等. 2015. 人端粒酶逆转录酶永生化MRC-5细胞方法的建立[J]. 中华实验和临床病毒学杂志, 29(02): 177-179. (Wu M, Yin J Z, Zhu W Yet al.2015. Establishment of immortalization method of human telomerase reverse transcriptase in MRC-5 cells[J] . Chinese Journal of Experimental and Clinical Virology, 29(02): 177-179. ) [14] 赵奇慧, 张恂, 申刚义等. 2019. 组织块贴壁法和混合酶消化法分离原代血管平滑肌细胞的表型特征比较[J] . 中国医药导刊, 21(05): 294-298. (Zhao Q H, Zhang X, Shen G Yet al.2019. Comparison of phenotypic characteristics of primary vascular smooth muscle cells isolated by tissue block adherence method and mixed enzyme digestion method[J]. Chinese Journal of Medicine, 21(05): 294-298.) [15] An K, Liu H P, Zhong X Let al.2017. hTERT-immortalized bone mesenchymal stromal cells expressing rat galanin via a single tetracycline-inducible lentivirus system[J]. Stem Cells International, 6082684 (doi: 10. 1155/ 2017/ 6082684). [16] Kawano Y, Kobune M, Yamaguchi M, et al.2003. Ex vivo expansion of human umbilical cord hematopoietic progenitor cells using a coculture system with human telomerase catalytic subunit (hTERT)-transfected human stromal cells[J]. Blood, 101(2): 532-540. [17] Li N F, Broad S, Lu Y Jet al.2007. Human ovarian surface epithelial cells immortalized with hTERT maintain functional prb and p53 expression[J]. Cell Proliferation, 40(5): 780-794. [18] Orsi N M, Reischl J B.2007. Mammalian embryo co-culture: Trials and tribulations of a misunderstood method[J]. Theriogenology, 67: 441-458. [19] Petkov S, Kahland T, Shomroni Oet al.2018. Immortalization of common marmoset monkey fibroblasts by piggybac transposition of hTERT[J]. PLOS ONE, 13(9): e0204580. [20] Shay J W, Wright W E.2005. Senescence and immortalization: Role of telomeres and telomerase[J] . Carcinogenesis, 26(5): 867-74. [21] Wang B., Jiang J., Zhang Yet al.2021. Combination of hde and biib021 efficiently inhibits cell proliferation and induces apoptosis via downregulating hTERT in myelodysplastic syndromes[J]. Experimental and Therapeutic Medicine, 21(5): 503-503. [22] Yeager T R, Reddel R R.1999. Constructing immortalized human cell lines[J]. Current Opinion in Biotechnology, 10(5): 465-469. [23] Yin B, Song Q, Chen Let al.2019. Establishment of an immortalized intestinal epithelial cell line from tree shrews by lentivirus-mediated hTERT gene transduction[J]. Cytotechnology, 71(1): 107-116. |
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