IL-6 amplifier activation in epithelial regions of bronchi after allogeneic lung transplantation

被引:36
作者
Lee, Jihye [1 ,2 ]
Nakagiri, Tomoyuki [3 ]
Kamimura, Daisuke [1 ,2 ]
Harada, Masaya [1 ,2 ]
Oto, Takahiro [4 ]
Susaki, Yoshiyuki [5 ]
Shintani, Yasushi [3 ]
Inoue, Masayoshi [3 ]
Miyoshi, Shinichiro [4 ]
Morii, Eiichi [5 ]
Hirano, Toshio [1 ,2 ,6 ]
Murakami, Masaaki [1 ,2 ]
Okumura, Meinoshin [3 ]
机构
[1] Osaka Univ, Grad Sch Frontier Biosci, Grad Sch Med, Lab Dev Immunol,JST CREST, Suita, Osaka 5650871, Japan
[2] Osaka Univ, WPI Immunol Frontier Res Ctr, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Med, Dept Gen Thorac Surg, Suita, Osaka 5650871, Japan
[4] Okayama Univ, Grad Sch Med, Dept Canc & Thorac Surg, Okayama 7008530, Japan
[5] Osaka Univ, Grad Sch Med, Dept Pathol, Suita, Osaka 5650871, Japan
[6] Osaka Univ, JST CREST, Suita, Osaka 5650871, Japan
基金
日本科学技术振兴机构;
关键词
cytokines; inflammation; NF?B; STAT3; IL-6; transplantation; POSITIVE-FEEDBACK; INTERLEUKIN-6; REJECTION;
D O I
10.1093/intimm/dxs158
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
An IL-6-triggered NF-B loop: the IL-6 amplifier occurs in epithelia of a transplanted human lung.The IL-6 amplifier, a positive feedback loop for NFB signaling, which was originally found to be activated by IL-17A and IL-6 stimulation in non-immune cells, is molecularly a simultaneous activator of NFB and signal transducer and activator of transcription 3 (STAT3), functionally a local chemokine inducer and pathologically a machinery for inflammation development. It has been shown that IL-6 amplifier activation in epithelial cells contributes to rejection responses in a mouse chronic rejection model that develops a bronchiolitis obliterans (BO)-like disease. We investigated whether the IL-6 amplifier is activated in BO regions of a human lung graft after allogeneic transplantation. NFB and STAT3 molecules were phosphorylated in the epithelial regions of bronchi that localized in the BO regions. Additionally, chemokine ligand 2 (CCL2), and CD4 T cells and macrophages increased in these regions. Furthermore, human lung epithelial cells expressed CCL2 after stimulation by IFN in the presence of IL-6 and epidermal growth factor via enhanced STAT3 signaling, which parallels behavior seen in the mouse model. Thus, our results suggest that the IL-6 amplifier in the epithelial cells of grafts is involved in chronic rejection after lung transplantation, suggesting that the amplifier may be a valuable therapeutic target to prevent chronic rejection after lung transplantation.
引用
收藏
页码:319 / 332
页数:14
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