Targeted NF-κB inhibition of asthmatic serum-mediated human monocyte-derived dendritic cell differentiation in a transendothelial trafficking model

被引:26
作者
Gu, Xiao-Yan [1 ]
Zhou, Lin-Fu [1 ]
Zhang, Ming-Shun [2 ]
Dai, Wen-Jing [1 ]
Chen, Sai-Ying [3 ]
He, Shao-Heng [1 ]
Ji, Xiao-Hui [2 ]
Yin, Kai-Sheng [1 ]
机构
[1] Nanjing Med Univ, Dept Resp Med, Affiliated Hosp 1, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Dept Microbiol & Immunol, Nanjing 210029, Peoples R China
[3] 81st Hosp Chinese PLA, Dept Obstet & Gynecol, Nanjing 210002, Peoples R China
基金
中国国家自然科学基金;
关键词
Asthma; Monocyte; Dendritic cell; NF-kappa B; Transendothelial trafficking model; CD4(+) T-CELLS; ACTIVATION; ADENOVIRUS; ALPHA; MATURATION; ALLERGEN; EXPRESSION; RESPONSES; STRATEGY; BLOCKADE;
D O I
10.1016/j.cellimm.2009.07.001
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Transendothelial trafficking model mimics in vivo differentiation of monocytes into dendritic cells (DC). The serum from patients with systemic lupus erythematosus promotes the differentiation of monocytes into mature DC. We have shown that selective inhibition of NF-kappa B by adenoviral gene transfer of a novel mutated I kappa B alpha (AdI kappa B alpha M) in DC contributes to T cell tolerance. Here we demonstrated for the first time that asthmatic serum facilitated human monocyte-derived DC (MDDC) maturation associated with increased NF-kappa B activation in this model. Furthermore, selective blockade of NF-kappa B by AdI kappa B alpha M in MDDC led to increased apoptosis, and decreased levels of CD80, CD83, CD86, and IL-12 p70 but not IL-10 in asthmatic serum-stimulated MDDC, accompanied by reduced proliferation of T cells. These results suggest that AdI kappa B alpha M-tramsferred MDDC are at a more immature stage which is beneficial to augment the immune tolerance in asthma. (C) 2009 Elsevier Inc. All rights reserved
引用
收藏
页码:14 / 20
页数:7
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