Journal
CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY
Volume 40, Issue 3, Pages 276-282Publisher
TERMEDIA PUBLISHING HOUSE LTD
DOI: 10.5114/ceji.2015.54586
Keywords
p38; interleukin 6; cytokine; lipopolysaccharide; macrophage
Categories
Funding
- National Science Foundation of China [81071535]
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The p38 mitogen-activated protein kinase (MAPK) plays a key role in lipopolysaccharide (LPS)-induced signal transduction pathways that lead to inflammatory cytokine synthesis in macrophages; however, whether the inhibition of p38 MAPK regulates LPS-induced inflammatory cytokine expression in different types of macrophages remains the subject of debate. Herein, we assessed whether the inhibition of p38 MAPK by SB203580 regulates LPS-induced expression of the inflammatory cytokines tumor necrosis factor alpha (TNF-alpha) and interleukin 6 (IL-6) in RAW264.7 and resident peritoneal macrophages. Lipopolysaccharide stimulation of RAW264.7 macrophages or mouse resident peritoneal macrophages significantly increased TNF-a and IL-6 production. The addition of SB203580 to cultures dramatically blocked LPS-induced TNF-a production in RA W264.7 and mouse resident peritoneal macrophages, and dramatically blocked LPS-induced IL-6 production in RA W264.7 macrophages, but not in mouse resident peritoneal macrophages. Additionally, high concentrations of SB203580 resulted in increased IL-6 production. However, LPS-stimulation significantly up-regulated the mRNA transcript levels of TNF-a and IL-6 in RAW264.7 and mouse resident peritoneal macrophages, whereas pretreatment with SB203580 dramatically down-regulated LPS-induced mRNA transcript levels of TNF-alpha and IL-6 in these cells. Our data show that SB203580 differentially modulates LPS-induced production of the inflammatory cytokine IL-6 in two different sources of macrophages, and that this course of regulation occurs at the IL-6 mRNA post-transcriptional stage.
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