Essential Roles of IL-6 Trans-Signaling in Colonic Epithelial Cells, Induced by the IL-6/Soluble-IL-6 Receptor Derived from Lamina Propria Macrophages, on the Development of Colitis-Associated Premalignant Cancer in a Murine Model

被引:174
|
作者
Matsumoto, Satoshi [1 ]
Hara, Theko [1 ]
Mitsuyama, Keiichi [2 ]
Yamamoto, Mayuko [1 ]
Tsuruta, Osamu [2 ]
Sata, Michio [2 ]
Scheller, Juergen [3 ]
Rose-John, Stefan [3 ]
Kado, Sho-ichi [1 ]
Takada, Toshihiko [1 ]
机构
[1] Yakult Cent Inst Microbiol Res, Tokyo 1868650, Japan
[2] Kurume Univ, Sch Med, Dept Med, Div Gastroenterol, Kurume, Fukuoka 830, Japan
[3] Univ Kiel, Dept Biochem, Kiel, Germany
来源
JOURNAL OF IMMUNOLOGY | 2010年 / 184卷 / 03期
关键词
INFLAMMATORY-BOWEL-DISEASE; DEXTRAN SULFATE SODIUM; ULCERATIVE-COLITIS; STAT3; ACTIVATION; INTESTINAL INFLAMMATION; REGULATED EXPRESSION; COLORECTAL-CANCER; SOLUBLE RECEPTORS; GROWTH-FACTOR; CUTTING EDGE;
D O I
10.4049/jimmunol.0801217
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activation of the IL-6/Stat3 via IL-6 trans-signaling plays an important role in the pathogenesis of inflammatory bowel disease. Colitis-associated cancer (CAC) is a large bowel cancer and occurs with long-standing inflammatory bowel disease. The role of the 1L-6/Stat3 in the development of CAC has not been fully understood. We investigate whether IL-6 traits-signaling contributes to the development of CAC using a mouse colitis-associated premalignant cancer (CApC) model. Chronic colitis (CC) was induced in BALB/c mice using dextran sodium sulfate. CApC was induced by dextran sodium sulfate treatment to CC-affected mice. IL-6 expression was determined by quantitative RT-PCR and immunofluorescence staining in colon. Phospho-Stat3 expression was examined by Western blotting and immunofluorescence analysis. The expression of IL-6 receptors (i.e., the IL-6R alpha-chain and gp130) and tumor necrosis factor-a converting enzyme in the colon was examined by laser-capture microdissection and immunofluorescence staining. Soluble IL-6R alpha (sIL-6R alpha) was examined by Western blotting of epithelial cell-depleted colonic tissues. We also investigated whether a soluble gp130-Fc fusion protein could prevent CApC. IL-6 expression was increased in the colon of CC- and CApC-affected mice and was restricted to lamina propria-macrophages. The expression of IL-6R alpha and tumor necrosis factor-alpha converting enzyme was increased in the lamina propria CD11b-macrophages of CC-affected mice. sIL-6R alpha expression was also increased in these tissues. Reduced levels of IL-6R alpha generation were observed in the colonic epithelial cells of CC- and CApC-affected mice and were associated with the increased expression of gp130 and phospho-Stat3. Treatment with soluble gp130Fc significantly reduced the CApC. IL-6 trans-signaling in epithelial cells induced by macrophage-derived IL-6/sIL-6R alpha plays a crucial role in the development of CAC. The Journal of Immunology, 2010, 184: 1543-1551.
引用
收藏
页码:1543 / 1551
页数:9
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