TY - JOUR
T1 - Immortalization of Fetal Bovine Colon Epithelial Cells by Expression of Human Cyclin D1, Mutant Cyclin Dependent Kinase 4, and Telomerase Reverse Transcriptase
T2 - An in Vitro Model for Bacterial Infection
AU - Kuroda, Kengo
AU - Kiyono, Tohru
AU - Isogai, Emiko
AU - Masuda, Mizuki
AU - Narita, Moe
AU - Okuno, Katsuya
AU - Koyanagi, Yukako
AU - Fukuda, Tomokazu
N1 - Funding Information:
This study is one of the national projects associated with the Great East Japan Earthquake and has been entirely endorsed and supported by the Japanese government through the Ministry of Education, Culture, Sports, Science and Technology, Japan, and the detailed description of the animal care and protocols is described in our previous study []. In briefly, we collected organs and tissues from the euthanized cattle by the combined unit of veterinary doctors belonging to the Livestock Hygiene Service Center (LHSC) of Fukushima Prefecture and those belonging to the Ministry of Agriculture, Forestry and Fisheries, Japan. Cattle were sacrificed by these veterinarians by the following method according to the Regulation for Animal Experiments and Related Activities at Tohoku University (Regulation No: 2014kado-037). Cattle were sacrificed by exanguination from the jugular vein in their unconscious state by a pentobarbital (2 mg/kg) and suxamethonium (10 ml/kg) after intramuscular injection of hypnotics (xylazine hydrochloride, 0.2 mg/kg).
Publisher Copyright:
© 2015 Kuroda et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2015/12/1
Y1 - 2015/12/1
N2 - Cattle are the economically important animals in human society. They are essential for the production of livestock products such as milk and meats. The production efficiency of livestock products is negatively impacted by infection with zoonotic pathogens. To prevent and control infectious diseases, it is important to understand the interaction between cattle tissue and pathogenic bacteria. In this study, we established an in vitro infection model of an immortalized bovine colon-derived epithelial cell line by transducing the cells with lentiviral vectors containing genes encoding cell cycle regulators cyclin D1, mutant cyclin dependent kinase 4 (CDK4), and human telomerase reverse transcriptase (TERT). The established cell line showed continuous cell proliferation, expression of epithelial markers, and an intact karyotype, indicating that the cells maintained their original nature as colon-derived epithelium. Furthermore, we exposed the established cell line to two strains of Salmonella enterica and EHEC. Interestingly, S. Typhimurium showed higher affinity for the established cell line and invaded the cytoplasm than S. Enteritidis. Quantitative RT-PCR revealed that gene expression of Toll-like receptor 1 (TLR1), TLR 2 and TLR 3, whereas TLR 4, 5 and 6 were not detectable in established cells. Our established immortalized colon-derived epithelial cell should be a useful tool for studies evaluating the molecular mechanisms underlying bacterial infection.
AB - Cattle are the economically important animals in human society. They are essential for the production of livestock products such as milk and meats. The production efficiency of livestock products is negatively impacted by infection with zoonotic pathogens. To prevent and control infectious diseases, it is important to understand the interaction between cattle tissue and pathogenic bacteria. In this study, we established an in vitro infection model of an immortalized bovine colon-derived epithelial cell line by transducing the cells with lentiviral vectors containing genes encoding cell cycle regulators cyclin D1, mutant cyclin dependent kinase 4 (CDK4), and human telomerase reverse transcriptase (TERT). The established cell line showed continuous cell proliferation, expression of epithelial markers, and an intact karyotype, indicating that the cells maintained their original nature as colon-derived epithelium. Furthermore, we exposed the established cell line to two strains of Salmonella enterica and EHEC. Interestingly, S. Typhimurium showed higher affinity for the established cell line and invaded the cytoplasm than S. Enteritidis. Quantitative RT-PCR revealed that gene expression of Toll-like receptor 1 (TLR1), TLR 2 and TLR 3, whereas TLR 4, 5 and 6 were not detectable in established cells. Our established immortalized colon-derived epithelial cell should be a useful tool for studies evaluating the molecular mechanisms underlying bacterial infection.
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U2 - 10.1371/journal.pone.0143473
DO - 10.1371/journal.pone.0143473
M3 - Article
C2 - 26624883
AN - SCOPUS:84955598394
SN - 1932-6203
VL - 10
JO - PLoS One
JF - PLoS One
IS - 12
M1 - e0143473
ER -