Eng Hock-Liew, Hsu Yuan-Ying, Lin Tsun-Mei
Department of Pathology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, 833, Taiwan.
Department of Pathology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, 833, Taiwan.
Biochem Biophys Res Commun. 2018 Feb 26;497(1):319-325. doi: 10.1016/j.bbrc.2018.02.079. Epub 2018 Feb 12.
The recognition of single-stranded RNA by TLR7/8 leads to the production of NF-κB-mediated cytokines and type I IFNs. However, the role of TLR7/8 activation in monocytes and macrophages is still unclear. The aim of this study was to investigate the differences in the activation of TLR7/8 between these two cell types. Microarray analysis, qRT-PCR and flow cytometry were used to analyse TLR7/8 signalling pathways in monocytes and macrophages after stimulation with agonists. Our data indicated that TLR8 agonists activated the NF-κB- and IRF-mediated pathways in THP-1 cells, whereas TLR7 agonists did not. However, silent TLR8 and enhanced TLR7 expression could increase TLR7-induced NF-κB activation in monocytes. TLR7 and TLR8 agonists induced NF-κB activation but no ISG response in PMA-differentiated THP-1 cells. The mRNA levels of pro-inflammatory cytokine were elevated upon CL075 stimulation in macrophages compared to monocytes. Thus, TLR7 and TLR8 might modulate different immune responses in monocytes and macrophages.
TLR7/8对单链RNA的识别会导致NF-κB介导的细胞因子和I型干扰素的产生。然而,TLR7/8激活在单核细胞和巨噬细胞中的作用仍不清楚。本研究的目的是调查这两种细胞类型之间TLR7/8激活的差异。使用微阵列分析、qRT-PCR和流式细胞术分析激动剂刺激后单核细胞和巨噬细胞中TLR7/8信号通路。我们的数据表明,TLR8激动剂可激活THP-1细胞中NF-κB和IRF介导的通路,而TLR7激动剂则不能。然而,沉默TLR8并增强TLR7表达可增加单核细胞中TLR7诱导的NF-κB激活。TLR7和TLR8激动剂在PMA分化的THP-1细胞中诱导NF-κB激活,但无ISG反应。与单核细胞相比,巨噬细胞在CL075刺激后促炎细胞因子的mRNA水平升高。因此,TLR7和TLR8可能在单核细胞和巨噬细胞中调节不同的免疫反应。