The effect of regulator proteins on the IFN-γ/TLR9 synergistic signal transduction
- VernacularTitle:IFN-γ/TLR9-ийн харилцан дэмжих үйлчлэлд зохицуулагч молекулын нөлөө
- Author:
Baljinnyam T
1
,
2
;
Khulan O
2
;
Erkhembayar Sh
3
;
Baasansuren E
2
;
Jawkhlan B
2
;
Batkhishig
2
;
Enkhsaikhan L
2
;
Galindew B
2
;
Tsewelmaa N
2
;
Baigalmaa B
2
;
Hongorzul B
2
;
Sodnomtsogt L
2
;
Nyambayar D
2
;
Batbaatar G
2
;
Monhbat B
2
;
Munkhtuwshin N
1
;
Bilegtsaikhan Ts
1
,
2
Author Information
- Publication Type:Journal Article
- From: Health Laboratory 2018;8(1):8-13
- CountryMongolia
- Language:Mongolian
-
Abstract:
Introduction:When human body encounters external pathogens primary/innate immunity cells are activated by recognizing them and secondary/adaptive immunity is activated consecutively. Immune cell surface receptors, called Toll-like receptors (TLRs) recognize and bind pathogens. In our previous study, we revealed that there is a synergistic action between TLR9 and IFN-γ signaling in the endothelial cells.
Purpose:To determine the role of negative and positive regulatory proteins on the IFN-γ/TLR9 synergistic signaling pathway
Materials and Methods:This study was held in the Core Laboratory, Science Technology Center, Mongolian National University of Medical Sciences (MNUMS). In this study, murine endothelial cell (END-D) culture was used. The negative and positive regulator protein expression was detected by Western blotting.
Result:Result of immunoblotting assay indicated that CpG DNA enhanced IFN-γ positive regulator protein p38 phosphorylation in the endothelial cells. Treatment by TLR9 ligand CpG DNA and IFN-γ increased p38 activation in 0.5 hour and 1 hour. CpG DNA inhibited IFN-γ negative regulator SOCS1 protein expression in 4 hr and 8 hr. Therefore, TLR9 ligand CpG DNA increased IFN-γ signal transduction in the endothelial cell line.
Conclusion:TLR9 ligand CpG DNA has decreased IFN-γ negative regulator protein SOCS1 expression. CpG DNA has increased IFN-γ positive regulator protein p38 phosphorylation. - Full text:HL-2018-8(2)-8-13.pdf