Lipopolysaccharide-induced expression of Th1/Th2 cytokines in whole neonatal cord and adult blood: role of nuclear factor-kappa B and p38 MAPK

Neonatology. 2011;99(2):140-5. doi: 10.1159/000313967. Epub 2010 Aug 27.

Abstract

Background: Sepsis continues to be a leading cause of morbidity and mortality in newborns.

Objective: As both nuclear factor-kappa B (NF-κB) and p38 mitogen-activated protein kinase (MAPK) appear to be critical mediators in inflammatory response, we studied the effects of lipopolysaccharide (LPS) on expression and function of NF-κB and p38 MAPK in whole neonatal cord and adult blood.

Methods: Th1/Th2 cytokine concentrations and phosphorylation of NF-κB and p38 MAPK were determined by flow-cytometric analysis.

Results: Tumor necrosis factor-alpha (TNF-α), IL-6, and IL-10 concentrations were significantly elevated in supernatants of neonatal and adult blood after LPS stimulation for 4 h. IFN-γ, IL-4, and IL-2 showed no significant alterations. Furthermore, TNF-α concentrations were significantly higher in adult compared to neonatal blood after LPS stimulation. Stimulation with LPS resulted in significantly decreased activation of p38 MAPK in neonatal blood, whereas NF-κB showed no difference. Following inhibition of p38 MAPK with the specific inhibitor SB-202190, levels of TNF-α and IL-6 significantly decreased in neonatal and adult blood, whereas pharmacological inhibition of NF-κB with SC-514 showed no significant effect on cytokine expression.

Conclusions: We conclude that p38 MAPK phosphorylation is crucially involved in LPS activation and could explain the differences in early cytokine response between neonatal and adult blood.

MeSH terms

  • Adult
  • Cytokines / biosynthesis*
  • Cytokines / blood
  • Enzyme Inhibitors / pharmacology
  • Fetal Blood / drug effects
  • Fetal Blood / enzymology
  • Fetal Blood / immunology*
  • Flow Cytometry
  • Humans
  • Imidazoles / pharmacology
  • Infant, Newborn
  • Lipopolysaccharides / pharmacology*
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / biosynthesis
  • NF-kappa B / blood
  • Phosphorylation / drug effects
  • Pyridines / pharmacology
  • Signal Transduction
  • Th1 Cells / drug effects
  • Th1 Cells / enzymology
  • Th1 Cells / immunology
  • Th1 Cells / metabolism*
  • Th2 Cells / drug effects
  • Th2 Cells / enzymology
  • Th2 Cells / immunology
  • Th2 Cells / metabolism*
  • Thiophenes / pharmacology
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • p38 Mitogen-Activated Protein Kinases / biosynthesis*
  • p38 Mitogen-Activated Protein Kinases / blood

Substances

  • Cytokines
  • Enzyme Inhibitors
  • Imidazoles
  • Lipopolysaccharides
  • NF-kappa B
  • Pyridines
  • SC 514
  • Thiophenes
  • p38 Mitogen-Activated Protein Kinases
  • 4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)imidazole