Macrophages produce IL-33 by activating MAPK signaling pathway during RSV infection
Feifei Qi1, Song Bai1, Dandan Wang1
1Department of Immunology, School of Basic Medical Science, China Medical University, Shenyang, China.
Abstract:
It has been reported that RSV infection can enhance IL-33 production in lung macrophages. However, little is known about specific signaling pathways for activation of macrophages during RSV infection. In the present study, by using real-time RT-PCR as well as western blot assay, it became clear that RSV infection can enhance not only the expression of mRNAs for MAPK molecules (including p38, JNK1/2, and ERK1/2), but also the levels of MAPK proteins in lung macrophages as well as RAW264.7 cells. Furthermore, infection with RSV resulted in an increased level of phosphorylated MAPK proteins in RAW264.7 cells, suggesting that MAPK signaling pathway may participate in the process of RSV-induced IL-33 secretion by macrophages. In fact, the elevated production of IL-33 in RAW264.7 was attenuated significantly by pretreatment of the cells with special MAPK inhibitor before RSV infection, further confirming the function of MAPKs pathway in RSV-induced IL-33 production in macrophages. In contrast, the expression of NF-κB mRNA as well as the production of NF-κB protein in lung macrophages and RAW264.7 cells was not enhanced markedly after RSV infection. Moreover, RSV infection failed to induce the phosphorylation of NF-κB in RAW264.7 cells, suggesting that NF-κB signaling pathway may be not involved in RSV-induced IL-33 production in macrophages. Conclusion, these results indicate that RSV-induced production of IL-33 in macrophages is dependent on the activation of MAPK signaling pathway.
Insights
Respiratory Syncytial Virus (RSV) infection activates macrophages to produce Interleukin-33 (IL-33) via the Mitogen-Activated Protein Kinase (MAPK) signaling pathway, not the NF-κB pathway.
Area of Science:
- Immunology
- Virology
- Cell Biology
Background:
- Respiratory Syncytial Virus (RSV) infection is known to increase Interleukin-33 (IL-33) production in lung macrophages.
- Specific signaling pathways regulating macrophage activation during RSV infection remain largely unknown.
Purpose of the Study:
- To investigate the role of Mitogen-Activated Protein Kinase (MAPK) and Nuclear Factor kappa B (NF-κB) signaling pathways in RSV-induced IL-33 production by macrophages.
Main Methods:
- Real-time RT-PCR and Western blot assays were used to analyze gene and protein expression.
- RAW264.7 cells and primary lung macrophages were infected with RSV.
- MAPK and NF-κB signaling pathway activation was assessed via phosphorylation levels.
- The effect of MAPK inhibitors on IL-33 production was evaluated.
Main Results:
- RSV infection significantly enhanced mRNA and protein expression of MAPK molecules (p38, JNK1/2, ERK1/2) in macrophages.
- RSV infection led to increased phosphorylation of MAPK proteins, indicating pathway activation.
- Inhibition of MAPK signaling pathways significantly reduced RSV-induced IL-33 production.
- RSV infection did not markedly enhance NF-κB mRNA or protein expression, nor did it induce NF-κB phosphorylation.
Conclusions:
- RSV-induced IL-33 production in macrophages is dependent on the activation of the MAPK signaling pathway.
- The NF-κB signaling pathway does not appear to be involved in this process.
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