4.0 Article

Regulation of Differentiation and Function of Helper T Cells by Lymphocyte-Derived Catecholamines via α1- and β2- Adrenoceptors

Journal

NEUROIMMUNOMODULATION
Volume 22, Issue 3, Pages 138-151

Publisher

KARGER
DOI: 10.1159/000360579

Keywords

Adrenoceptors; Catecholamines; Interferon-gamma; Interleukin-4; Th1/Th2

Funding

  1. National Natural Science Foundation of China [81271323, 31371182]
  2. Natural Science Foundation of Jiangsu Province of China [BK2011386]
  3. Nantong Applied Research Program of China [BK2012014, BK2012015, CP12012003]
  4. Natural Science Foundation of Nantong University [09B14, 12Z003]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions

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Objective: Recently, we have reported that lymphocyte-derived endogenous catecholamines (CAs) facilitate a shift in the T helper (Th)1/Th2 balance towards Th2. The purpose of this study was to explore the involvement of adrenoreceptors (ARs) in Th differentiation and function modulation by lymphocyte-derived CAs. Methods: Lymphocytes were separated from the mesenteric lymph nodes of mice, stimulated with concanavalin A (Con A) and treated with pargyline, an inhibitor of CA degradation. Results: Pargyline downregulated the expression of Th1-relative factors, T-bet, interferon (IFN)-gamma and interleukin (IL)-2, but upregulated the expression of Th2-relative factors, GATA-3, IL-4 and IL-10. Pargyline reduced the percentage of IFN-gamma-producing CD4+ cells and the CD4+ IFN-gamma+/CD4+IL-4+cell ratio, although it did not alter the proportion of IL-4-producing CD4+ cells. In addition, the percentage of CD4+CD26+T cells and the CD4+CD26+/CD4+CD30+ cell ratio were also reduced in the pargylinetreated group. Furthermore, Con A-activated T cells treated with pargyline produced a lower level of IFN-gamma and a higher level of IL-4 than the control group. All these effects were blocked by the alpha(1)-AR antagonist corynanthine or the beta(2)-AR antagonist ICI 118551, but not by the alpha(2)-AR antagonist yohimbine or beta(1)-AR antagonist atenolol. Conclusions: These results imply that lymphocyte-derived CAs promote polarization of differentiation and function towards Th2 cells and that this effect is mediated by alpha(1)-AR and beta(2)-AR. (C) 2014 S. Karger AG, Basel

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