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通过慢病毒介导的hTERT基因转导建立树鼩永生化肠上皮细胞系。

Establishment of an immortalized intestinal epithelial cell line from tree shrews by lentivirus-mediated hTERT gene transduction.

作者信息

Yin Bowen, Song Qingkai, Chen Lingxia, Li Xiaofei, Han Yuanyuan, Wang Xuan, Dai Jiejie, Sun Xiaomei

机构信息

Center of Tree Shrew Germplasm Resources, Institute of Medical Biology, The Chinese Academy of Medical Science, Peking Union Medical College, Jiaoling Road 935, Kunming, 650118, China.

出版信息

Cytotechnology. 2019 Feb;71(1):107-116. doi: 10.1007/s10616-018-0270-0. Epub 2019 Jan 2.

Abstract

The intestinal epithelium has an average lifespan of 4-5 days. Normally, primary intestinal epithelial cells can be cultured for about 15 days in vitro. The aim of this study was to explore methods to isolate and immortalize intestinal epithelial cells (IECs) of tree shrews in order to establish a new resource of experimental material and to provide a cell model for drug development and infection mechanism research. Tissue from the small intestine of tree shrews was digested with collagenase XI, neutral protease I, and dithiothreitol. The human telomerase reverse transcriptase gene (hTERT) was transferred into tree shrew IECs using the pHBLV-CMVIE-ZsGreen-Puro vector. The level of hTERT mRNA was detected by quantitative reverse transcription polymerase chain reaction. Immunofluorescence and western blot assays were performed to detect biochemical markers of IECs. The micromorphology of cells was observed with electron microscopy. We then conducted experiments to assess proliferative activity and analyze the karyotype of isolated cells. The results showed the immortalized cell line that we established and screened, maintained the characteristics and biochemical markers of primary IECs. Our results showed that the cell line we established can be considered an alternative cell model for intestinal drug research and for studies on intestinal infection and cell signaling.

摘要

肠上皮的平均寿命为4 - 5天。正常情况下,原代肠上皮细胞在体外可培养约15天。本研究的目的是探索分离和永生化树鼩肠上皮细胞(IECs)的方法,以建立新的实验材料资源,并为药物开发和感染机制研究提供细胞模型。用XI型胶原酶、I型中性蛋白酶和二硫苏糖醇消化树鼩小肠组织。使用pHBLV - CMVIE - ZsGreen - Puro载体将人端粒酶逆转录酶基因(hTERT)转入树鼩IECs。通过定量逆转录聚合酶链反应检测hTERT mRNA水平。进行免疫荧光和蛋白质印迹分析以检测IECs的生化标志物。用电子显微镜观察细胞的微观形态。然后我们进行实验评估增殖活性并分析分离细胞的核型。结果表明,我们建立并筛选的永生化细胞系保持了原代IECs的特征和生化标志物。我们的结果表明,我们建立的细胞系可被视为用于肠道药物研究以及肠道感染和细胞信号传导研究的替代细胞模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03b4/6368523/e55a50eab0f1/10616_2018_270_Fig1_HTML.jpg

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