Norepinephrine modulates human dendritic cell activation by altering cytokine release. Academic Article uri icon

Overview

abstract

  • Norepinephrine (NE) can modulate dendritic cell (DC) activation in animal models, but the response of human DC to NE and other response modifiers is as yet not completely understood. Here we report the effect of NE on the cytokine response of a mixed population of human DC cells to extracellular stimuli. These cells were obtained by differentiating human cord blood CD34+ precursor cells. NE inhibited the lipopolysaccharide (LPS)-stimulated production of interleukin (IL)-23, IL-12 p40, tumor necrosis factor (TNF)-alpha and IL-6 whereas the expression of IL-10 was not significantly affected. Thus, human cord blood-derived DC respond to NE in a manner similar to mouse Langerhans cells (LC). Furthermore, forskolin also inhibited the LPS-induced levels of TNF-alpha, IL-12 p40, IL-23 p19 and IL-6, supporting the hypothesis that the effects of NE are mediated by cAMP. Data from experiments using inhibitors of adrenergic receptors suggest that NE acts through beta-adrenergic receptors. As IL-23 promotes the differentiation of CD4+ T cells required for T(H)1-mediated immunity, we suggest that NE decreases the differentiation of CD4+ T cells needed for T(H)1-mediated contact hypersensitivity and that NE is a candidate regulator of human DC functions in the skin.

publication date

  • January 16, 2008

Research

keywords

  • Dendritic Cells
  • Interleukins
  • Lipopolysaccharides
  • Norepinephrine
  • Sympathomimetics
  • Tumor Necrosis Factor-alpha

Identity

Scopus Document Identifier

  • 39049117323

Digital Object Identifier (DOI)

  • 10.1111/j.1600-0625.2007.00677.x

PubMed ID

  • 18205818

Additional Document Info

volume

  • 17

issue

  • 3