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Characterization and anti-inflammation role of swine IFITM3 gene

IFITM3 is involved in cell adhesion, apoptosis, immune, and antivirus activity. Furthermore, IFITM3 gene has been considered as a preferential marker for inflammatory diseases, and positive correlation to pathological grades. Therefore, we assumed that IFITM3 was regulated by different signal pathwa...

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Autores principales: Li, He-Ping, Chen, Pei-Ge, Liu, Fu-Tao, Zhu, He-Shui, Jiao, Xian-Qin, Zhong, Kai, Guo, Yu-Jie, Zha, Guang-Ming, Han, Li-Qiang, Lu, Wei-Fei, Wang, Yue-Ying, Yang, Guo-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650283/
https://www.ncbi.nlm.nih.gov/pubmed/29088728
http://dx.doi.org/10.18632/oncotarget.20568
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author Li, He-Ping
Chen, Pei-Ge
Liu, Fu-Tao
Zhu, He-Shui
Jiao, Xian-Qin
Zhong, Kai
Guo, Yu-Jie
Zha, Guang-Ming
Han, Li-Qiang
Lu, Wei-Fei
Wang, Yue-Ying
Yang, Guo-Yu
author_facet Li, He-Ping
Chen, Pei-Ge
Liu, Fu-Tao
Zhu, He-Shui
Jiao, Xian-Qin
Zhong, Kai
Guo, Yu-Jie
Zha, Guang-Ming
Han, Li-Qiang
Lu, Wei-Fei
Wang, Yue-Ying
Yang, Guo-Yu
author_sort Li, He-Ping
collection PubMed
description IFITM3 is involved in cell adhesion, apoptosis, immune, and antivirus activity. Furthermore, IFITM3 gene has been considered as a preferential marker for inflammatory diseases, and positive correlation to pathological grades. Therefore, we assumed that IFITM3 was regulated by different signal pathways. To better understand IFITM3 function in inflammatory response, we cloned swine IFITM3 gene, and detected IFITM3 distribution in tissues, as well as characterized this gene. Results indicated that the length of swine IFITM3 gene was 438 bp, encoding 145 amino acids. IFITM3 gene expression abundance was higher in spleen and lungs. Moreover, we next constructed the eukaryotic expression vector PBIFM3 and transfected into PK15 cells, finally obtained swine IFITM3 gene stable expression cell line. Meanwhile, we explored the effects of LPS on swine IFITM3 expression. Results showed that LPS increased IFITM3 mRNA abundance and exhibited time-dependent effect for LPS treatment. To further demonstrate the mechanism that IFITM3 regulated type I IFNs production, we also detected the important molecules expression of TLR4 signaling pathway. In transfected and non-transfected IFITM3 PK15 cells, LPS exacerbated the relative expression of TLR4-NFκB signaling molecules. However, the IFITM3 overexpression suppressed the inflammatory development of PK15 cells. In conclusion, these data indicated that the overexpression of swine IFITM3 could decrease the inflammatory response through TLR4 signaling pathway, and participate in type I interferon production. These findings may lead to an improved understanding of the biological function of IFITM3 in inflammation.
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spelling pubmed-56502832017-10-30 Characterization and anti-inflammation role of swine IFITM3 gene Li, He-Ping Chen, Pei-Ge Liu, Fu-Tao Zhu, He-Shui Jiao, Xian-Qin Zhong, Kai Guo, Yu-Jie Zha, Guang-Ming Han, Li-Qiang Lu, Wei-Fei Wang, Yue-Ying Yang, Guo-Yu Oncotarget Research Paper: Immunology IFITM3 is involved in cell adhesion, apoptosis, immune, and antivirus activity. Furthermore, IFITM3 gene has been considered as a preferential marker for inflammatory diseases, and positive correlation to pathological grades. Therefore, we assumed that IFITM3 was regulated by different signal pathways. To better understand IFITM3 function in inflammatory response, we cloned swine IFITM3 gene, and detected IFITM3 distribution in tissues, as well as characterized this gene. Results indicated that the length of swine IFITM3 gene was 438 bp, encoding 145 amino acids. IFITM3 gene expression abundance was higher in spleen and lungs. Moreover, we next constructed the eukaryotic expression vector PBIFM3 and transfected into PK15 cells, finally obtained swine IFITM3 gene stable expression cell line. Meanwhile, we explored the effects of LPS on swine IFITM3 expression. Results showed that LPS increased IFITM3 mRNA abundance and exhibited time-dependent effect for LPS treatment. To further demonstrate the mechanism that IFITM3 regulated type I IFNs production, we also detected the important molecules expression of TLR4 signaling pathway. In transfected and non-transfected IFITM3 PK15 cells, LPS exacerbated the relative expression of TLR4-NFκB signaling molecules. However, the IFITM3 overexpression suppressed the inflammatory development of PK15 cells. In conclusion, these data indicated that the overexpression of swine IFITM3 could decrease the inflammatory response through TLR4 signaling pathway, and participate in type I interferon production. These findings may lead to an improved understanding of the biological function of IFITM3 in inflammation. Impact Journals LLC 2017-08-27 /pmc/articles/PMC5650283/ /pubmed/29088728 http://dx.doi.org/10.18632/oncotarget.20568 Text en Copyright: © 2017 Li et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper: Immunology
Li, He-Ping
Chen, Pei-Ge
Liu, Fu-Tao
Zhu, He-Shui
Jiao, Xian-Qin
Zhong, Kai
Guo, Yu-Jie
Zha, Guang-Ming
Han, Li-Qiang
Lu, Wei-Fei
Wang, Yue-Ying
Yang, Guo-Yu
Characterization and anti-inflammation role of swine IFITM3 gene
title Characterization and anti-inflammation role of swine IFITM3 gene
title_full Characterization and anti-inflammation role of swine IFITM3 gene
title_fullStr Characterization and anti-inflammation role of swine IFITM3 gene
title_full_unstemmed Characterization and anti-inflammation role of swine IFITM3 gene
title_short Characterization and anti-inflammation role of swine IFITM3 gene
title_sort characterization and anti-inflammation role of swine ifitm3 gene
topic Research Paper: Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650283/
https://www.ncbi.nlm.nih.gov/pubmed/29088728
http://dx.doi.org/10.18632/oncotarget.20568
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