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Published on: May 22, 2014
Pyocyanin from Pseudomonas induces IL-8 production through the PKC and NF-κB pathways in U937 cells
Wenshu Chai1, Jia Zhang, Zhitu Zhu
1Department of Respiratory Diseases, The First Affiliated Hospital, Liaoning Medical University, Jinzhou, Liaoning 121001, P.R. China.
Abstract:
Pyocyanin, an extracellular product of Pseudomonas aeruginosa (P. aeruginosa), is important in invasive pulmonary infection. Pseudomonas infections are characterized by a marked influx of polymorphonuclear cells (neutrophils). An increased release of interleukin-8 (IL-8), a potent neutrophil chemoattractant, in response to pyocyanin may contribute to the marked infiltration of neutrophils and subsequent neutrophil-mediated tissue damage observed in Pseudomonas-associated lung diseases. In order to explore the pathogenesis of pyocyanin on macrophages, we treated phorbol-12-myristate-13-acetate (PMA)-differentiated U937 cells with pyocyanin in vitro and explored the expression of IL-8 using reverse transcription polymerase chain reaction (RT-PCR) and enzyme-linked immunosorbent assay (ELISA). In the present study, we also investigated the activation of protein kinase C (PKC) and nuclear factor (NF)-κB in PMA-differentiated U937 cells by western blotting and immunohistochemical methods. It was found that pyocyanin increased IL-8 release and mRNA expression in differentiated U937 cells in a concentration- and time-dependent manner. Calphostin C (Cal C), a protein kinase C (PKC) inhibitor, and pyrrolidine dithiocarbamate (PDTC) , an NF-κB inhibitor, blocked IL-8 expression in a concentration-dependent manner in pyocyanin-induced U937 cells. We concluded that pyocyanin promotes IL-8 secretion and mRNA expression in a concentration- and time-dependent manner and furthermore, that the PKC and NF-κΒ signaling pathways may be involved in the expression of IL-8 in pyocyanin-infected PMA-differentiated U937 cells.
Insights
Pyocyanin from Pseudomonas aeruginosa increases interleukin-8 (IL-8) release and mRNA in U937 cells. Protein kinase C (PKC) and nuclear factor-kappa B (NF-κB) pathways mediate this pyocyanin-induced IL-8 expression, contributing to lung inflammation.
Area of Science:
- Microbiology
- Immunology
- Cell Biology
Background:
- Pseudomonas aeruginosa infections cause significant lung inflammation due to neutrophil infiltration.
- Pyocyanin, a P. aeruginosa toxin, is implicated in the pathogenesis of these infections.
- Interleukin-8 (IL-8) is a key chemoattractant for neutrophils, and its dysregulation contributes to tissue damage.
Purpose of the Study:
- To investigate the effect of pyocyanin on IL-8 expression in macrophages.
- To elucidate the signaling pathways involved in pyocyanin-induced IL-8 production.
Main Methods:
- U937 cells, differentiated with phorbol-12-myristate-13-acetate (PMA), were treated with pyocyanin.
- IL-8 mRNA and protein levels were assessed using RT-PCR and ELISA.
- Activation of protein kinase C (PKC) and nuclear factor-kappa B (NF-κB) was analyzed via western blotting and immunohistochemistry.
Main Results:
- Pyocyanin significantly increased IL-8 release and mRNA expression in a concentration- and time-dependent manner.
- Inhibition of PKC with Calphostin C (Cal C) and NF-κB with pyrrolidine dithiocarbamate (PDTC) blocked pyocyanin-induced IL-8 expression.
- Pyocyanin treatment led to the activation of PKC and NF-κB signaling pathways.
Conclusions:
- Pyocyanin promotes IL-8 secretion and mRNA expression in a dose- and time-dependent manner.
- The PKC and NF-κB signaling pathways are critically involved in pyocyanin-induced IL-8 expression in macrophages.
- These findings highlight a mechanism by which pyocyanin contributes to neutrophil recruitment and lung inflammation in P. aeruginosa infections.
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