Jaceosidin inhibits contact hypersensitivity in mice via down-regulating IFN-γ/STAT1/T-bet signaling in T cells.

Jaceosidin inhibits contact hypersensitivity in mice via down-regulating IFN-γ/STAT1/T-bet signaling in T cells.
复制标题

Jaceosidin 通过下调 T 细胞中的 IFN-γ/STAT1/T-bet 信号传导来抑制小鼠的接触性超敏反应。

DOI:
10.1016/j.ejphar.2010.10.068
复制
发表时间:
2011-01
影响因子:
5
通讯作者:
--
中科院分区:
医学2区
文献类型:
--
作者:

文献摘要

参考文献

相似文献

本研究旨在研究毛蒿黄酮类化合物jaceosidin在体内外对T淋巴细胞的免疫抑制作用,并进一步探讨其可能的分子机制。Jaceosidin可浓度依赖性地抑制刀豆球蛋白A(ConA)诱导的T细胞增殖和活化,并抑制活化T细胞分泌IL-2、TNF-α和IFN-γ等促炎细胞因子。进一步的研究表明,jaceosidin下调活化的T细胞中STAT 1的活化和T-bet的表达。此外,为了研究jaceosidin在体内的免疫抑制作用,在BALB/c小鼠上进行苦基氯(picryl chloride,PCl)诱导的耳接触性皮炎模型。Jaceosidin以剂量依赖性方式显著改善PCl诱导的耳肿胀,这是由于其抑制STAT 1/T-bet信号通路。总之,这些发现表明,jaceosidin通过抑制T细胞增殖和活化在体外和体内发挥其免疫抑制作用,这与其有效下调IFN-γ/STAT 1/T-bet信号通路密切相关。
In the present study, we aimed to investigate the immunosuppressive activity of jaceosidin, a flavone isolated from Artemisia vestita, on T lymphocytes both in vitro and in vivo, and further explore its potential molecular mechanism. Jaceosidin exerted a significant inhibition on the T cell proliferation and activation induced by concanavalin A (Con A) in a concentration-dependent manner and it also inhibited the secretion of the proinflammatory cytokines such as IL-2, TNF-α and IFN-γ of activated T cells. Further study showed that jaceosidin down-regulated STAT1 activation and T-bet expression in activated T cells. Moreover, in order to investigate the immunosuppressive effect of jaceosidin in vivo, the picryl chloride (PCl)-induced ear contact dermatitis model was performed on BALB/c mice. Jaceosidin significantly ameliorated PCl-induced ear swelling in a dose-dependent manner, which was due to its inhibition of the STAT1/T-bet signaling pathway. In summary, these findings suggest that jaceosidin exerts its immunosuppressive effect both in vitro and in vivo through inhibiting T cell proliferation and activation, which is closely associated with its potent down-regulation of the IFN-γ/STAT1/T-bet signaling pathway.
DOI: 10.1016/j.jep.2005.01.054
发表时间: 2005-04-26
影响因子: 5.4
作者:
Lee, HG;Yu, KA;Yoon, DY
通讯作者: Yoon, DY
DOI: 10.1016/s0270-9139(03)80236-7
发表时间: 2003
期刊: Hepatology
影响因子: 13.5
作者:
J. Siebler;S. Wirtz;M. Protschka;L. Glimcher;M. Blessing;P. Galle;M. Neurath
通讯作者: J. Siebler;S. Wirtz;M. Protschka;L. Glimcher;M. Blessing;P. Galle;M. Neurath
DOI: 10.1016/j.jaci.2005.08.032
发表时间: 2005-12-01
影响因子: 14.2
作者:
Fei, MJ;Wu, XF;Xu, Q
通讯作者: Xu, Q
DOI: 10.1016/j.intimp.2007.08.028
发表时间: 2007-12-15
影响因子: 5.6
作者:
Lee, Seung Hoon;Bae, Eun-Ah;Kim, Doniz-Hyun
通讯作者: Kim, Doniz-Hyun
DOI: 10.1016/j.hep.2003.09.020
发表时间: 2003-12-01
期刊: HEPATOLOGY
影响因子: 13.5
作者:
Siebler, J;Wirtz, S;Neurath, MF
通讯作者: Neurath, MF