细胞因子
肿瘤坏死因子α
内分泌学
细胞生物学
受体
人口
福斯科林
内科学
脐带血
化学
树突状细胞
生物
免疫学
免疫系统
医学
环境卫生
作者
Earl Goyarts,Mary S. Matsui,Tom Mammone,Anna M. Bender,John A. Wagner,Daniel Maes,Richard D. Granstein
标识
DOI:10.1111/j.1600-0625.2007.00677.x
摘要
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.
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