Please use this identifier to cite or link to this item: https://doi.org/10.18632/oncotarget.20568
Title: Characterization and anti-inflammation role of swine IFITM3 gene
Authors: Li, H.-P
Chen, P.-G
Liu, F.-T
Zhu, H.-S
Jiao, X.-Q
Zhong, K
Guo, Y.-J
Zha, G.-M
Han, L.-Q
Lu, W.-F 
Wang, Y.-Y
Yang, G.Y
Keywords: amino acid
immunoglobulin enhancer binding protein
interferon
lipopolysaccharide
messenger RNA
toll like receptor 4
animal cell
animal tissue
antiinflammatory activity
Article
biological activity
controlled study
cytokine production
eukaryotic expression vector
gene
gene expression
gene expression regulation
gene function
gene overexpression
gene vector
genetic code
genetic transfection
IFITM3 gene
inflammation
lung
molecular cloning
nonhuman
pig
PK-15 cell line
signal transduction
spleen
Issue Date: 2017
Citation: Li, H.-P, Chen, P.-G, Liu, F.-T, Zhu, H.-S, Jiao, X.-Q, Zhong, K, Guo, Y.-J, Zha, G.-M, Han, L.-Q, Lu, W.-F, Wang, Y.-Y, Yang, G.Y (2017). Characterization and anti-inflammation role of swine IFITM3 gene. Oncotarget 8 (43) : 73579-73589. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.20568
Rights: Attribution 4.0 International
Abstract: 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-NF?B 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. ? Li et al.
Source Title: Oncotarget
URI: https://scholarbank.nus.edu.sg/handle/10635/179547
ISSN: 19492553
DOI: 10.18632/oncotarget.20568
Rights: Attribution 4.0 International
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