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Construction of a telomerase-immortalized porcine tracheal epithelial cell model for swine-origin mycoplasma infection

文献类型: 外文期刊

作者: Xie Xing 1 ; Hao Fei 1 ; Wang Hai-yan 1 ; Pang Mao-da 2 ; Gan Yuan 1 ; Liu Bei-bei 1 ; Zhang Lei 1 ; Wei Yen-na 1 ; Chen Rong 1 ; Zhang Zhen-zhen 1 ; Bao Wen-bin 3 ; Bai Yun 1 ; Shao Guo-qing 1 ; Xiong Qi-yan 1 ; Feng Zhi-xin 1 ;

作者机构: 1.Jiangsu Acad Agr Sci, Inst Vet Med, Key Lab Vet Bioprod Engn, Minist Agr & Rural Affairs, Nanjing 210014, Peoples R China

2.Jiangsu Acad Agr Sci, Inst Food Safety & Nutr, Jiangsu Key Lab Food Qual & Safety, State Key Lab Cultivat Base,Minist Sci & Technol, Nanjing 210014, Peoples R China

3.Yangzhou Univ, Coll Anim Sci & Technol, Yangzhou 225009, Jiangsu, Peoples R China

关键词: porcine tracheal epithelial cells (PTECs); hTERT-PTECs; swine-origin mycoplasmas; adhesion; cell model

期刊名称:JOURNAL OF INTEGRATIVE AGRICULTURE ( 影响因子:4.384; 五年影响因子:4.021 )

ISSN: 2095-3119

年卷期: 2022 年 21 卷 2 期

页码:

收录情况: SCI

摘要: Primary porcine tracheal epithelial cells (PTECs) are an appropriate model for studying the molecular mechanism of various porcine respiratory diseases, including swine-origin mycoplasmas, which are isolated from respiratory tract of pigs and mainly found on the mucosal surface surrounding swine trachea. However, the short proliferation ability of primary PTECs greatly limits their lifespan. In this study, primary PTECs were carefully isolated and cultured, and immortal PTECs were constructed by transfecting primary PTECs with the recombinant constructed plasmid pEGFP-hTERT containing human telomerase reverse transcriptase (hTERT). Immortal PTECs (hTERT-PTECs) maintained both the morphological and functional characteristics of primary PTECs, as indicated by the expression of cytokeratin 18, cell-cycle analysis, proliferation assay, Western blotting, telomerase activity assay, karyotype analysis and quantitative RT-PCR. Compared to primary PTECs, hTERT-PTECs had an extended replicative lifespan, higher telomerase activity, and enhanced proliferative activity. In addition, this cell line resulted in a lack of transformed and grown tumors in nude mice, suggesting that it could be safely applied in further studies. Moreover, hTERT-PTECs were vulnerable to all swine-origin mycoplasmas through quantitative analysis as indicated by 50% color changing unit (CCU50) calculation, and no significant differences of adhesion ability between primary and immortal PTECs were observed. For the representative swine mycoplasma Mycoplasma hyopneumoniae (Mhp), except for DNA copies quantitative real-time PCR assay, indirect immunofluorescence assay and Western blotting analysis also depicted that hTERT-PTECs was able to adhere to different Mhp strains of different virulence. In summary, like primary PTECs, hTERT-PTECs could be widely used as an adhesion cell model for swine-origin mycoplasmas and in infection studies of various porcine respiratory pathogens.

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