Constitutive STAT3 activation in intestinal T cells from patients with Crohn's disease

被引:163
作者
Lovato, P
Brender, C
Agnholt, J
Kelsen, J
Kaltoft, K
Svejgaard, A
Eriksen, KW
Woetmann, A
Odum, N
机构
[1] Univ Copenhagen, Panum Inst, Inst Med Microbiol & Immunol, DK-2200 Copenhagen, Denmark
[2] Univ Copenhagen, Inst Mol Biol, DK-2200 Copenhagen, Denmark
[3] Aarhus Univ Hosp, Dept Med V, DK-8000 Aarhus, Denmark
[4] Aarhus Univ, Inst Human Genet, DK-8000 Aarhus C, Denmark
[5] Natl Univ Hosp, Tissue Typing Lab, Dept Clin Immunol, DK-2200 Copenhagen, Denmark
关键词
D O I
10.1074/jbc.M207999200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Via cytoplasmic signal transduction pathways, cytokines induce a variety of biological responses and modulate the outcome of inflammatory diseases and malignancies. Crohn's disease is a chronic inflammatory bowel disease of unknown etiology. Perturbation of the intestinal cytokine homeostasis is believed to play a pivotal role, but the pathogenesis of Crohn's disease is not fully understood. Here, we study intestinal T cells from Crohn's disease and healthy volunteers. We show that STAT3 and STAT4 are constitutively activated in Crohn's patients but not in healthy volunteers. The activation is specific, because other STAT proteins are not constitutively activated. Furthermore, the STAT3 regulated protein, SOCS3, is also constitutively expressed in Crohn's patients but not in healthy volunteers. Taken together, these data provide evidence of abnormal STAT/SOCS signaling in Crohn's disease. This aberrant activation, so far noted only in malignant cells, establish a new critical approach for better understanding the immunopathogenesis of Crohn's disease.
引用
收藏
页码:16777 / 16781
页数:5
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