Gender dependent importance of IRAK-1 in dextran sulfate sodium induced colitis

被引:16
作者
Berglund, Martin [1 ]
Thomas, James A. [2 ]
Fredin, Maria Fritsch [1 ,3 ]
Melgar, Silvia [4 ]
Hornquist, Elisabeth H. [1 ,5 ]
Hultgren, Olof H. [1 ,6 ]
机构
[1] Univ Gothenburg, Dept Microbiol & Immunol, Inst Biomed, Sahlgrenska Acad, S-40530 Gothenburg, Sweden
[2] Univ Texas SW Med Ctr Dallas, Dept Pediat & Mol Biol, Dallas, TX 75390 USA
[3] AstraZeneca R&D, Dept Biosci, Molndal, Sweden
[4] Natl Univ Ireland Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
[5] Univ Orebro, Dept Med, Sch Hlth & Med Sci, Orebro, Sweden
[6] Orebro Univ Hosp, Dept Clin Microbiol, Orebro, Sweden
基金
瑞典研究理事会;
关键词
TLR-signaling; Intestinal inflammation; Mucosal immunity; INFLAMMATORY-BOWEL-DISEASE; RECEPTOR-ASSOCIATED KINASE; ULCERATIVE-COLITIS; THYMIC INVOLUTION; INTERFERON-GAMMA; CROHNS-DISEASE; MICE LACKING; BALB/C MICE; IFN-GAMMA; ACTIVATION;
D O I
10.1016/j.cellimm.2009.05.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Toll-like receptor (TLR) signaling is important for the induction of pro-inflammatory cytokines and interferon (IFN)-inducible genes in response to bacterial and viral challenge. Interleukin-1 receptor-associated kinase-1 (IRAK-1) is a signaling kinase situated downstream of the adapter protein myeloid differentiation factor 88 (MyD88) in the TLR intracellular signaling cascade and is required for normal signal transduction through this pathway. We investigated the importance of IRAK-1 in intestinal inflammation by using the dextran sulfate sodium (DSS)-colitis model. We show that IRAK-1 deficient mice are protected against systemic signs of inflammation, i.e., weight loss and spleen enlargement compared to wild-type controls irrespective of gender. However, IRAK-1(-/y) males but not IRAK-1(-/-) females display significant protection against colitis and thymic atrophy compared to wild-type mice. Our results indicate a gender specific effect of IRAK-1 in the DSS-induced colitis, an interesting finding since the Irak-1 gene is located on the X-chromosome and several inflammatory diseases have a gender dependent incidence. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:27 / 32
页数:6
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