| Literature DB >> 12615922 |
Paola Lovato1, Christine Brender, Jørgen Agnholt, Jens Kelsen, Keld Kaltoft, Arne Svejgaard, Karsten Wessel Eriksen, Anders Woetmann, Niels Ødum.
Abstract
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.Entities:
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Year: 2003 PMID: 12615922 DOI: 10.1074/jbc.M207999200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157