Flagellin stimulation suppresses IL-7 secretion of intestinal epithelial cells

IL-7 is a cytokine, which regulates development, maintenance and proliferation of T lymphocytes within the human immune system. Production of IL-7 is observed in a sterile environment such as thymus or bone marrow. However, it is also known that intestinal epithelial cells (IECs) residing in close c...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2008-10, Vol.44 (1), p.57-64
Hauptverfasser: Yoshioka, Atsushi, Okamoto, Ryuichi, Oshima, Shigeru, Akiyama, Junko, Tsuchiya, Kiichiro, Nakamura, Tetsuya, Kanai, Takanori, Watanabe, Mamoru
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Sprache:eng
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Zusammenfassung:IL-7 is a cytokine, which regulates development, maintenance and proliferation of T lymphocytes within the human immune system. Production of IL-7 is observed in a sterile environment such as thymus or bone marrow. However, it is also known that intestinal epithelial cells (IECs) residing in close contact with numerous bacterial stimuli also produce IL-7. Here we show that secretion of IL-7 by IECs is significantly suppressed upon stimulation by various bacterial components, including flagellin. Analysis of the intracellular mechanism by which flagellin regulates IL-7 production revealed that flagellin down-regulates expression of the two major transcripts encoding IL-7. Surprisingly, such function of flagellin was independent from the known transcriptional regulation of the IL-7 gene, as no significant change was observed in the transcriptional activity regulated by the previously identified promoter region. As the stability of IL-7 mRNA also remained unchanged upon flagellin stimulation, results suggested the possible involvement of a yet unknown transcriptional regulation of the IL-7 gene. These results describe a novel regulation of IL-7 production by bacterial stimuli, presumably mediated via Toll-like receptors. The present system might contribute to regulate the local lymphocyte pool, in response to the gut luminal or sub-mucosal bacterial abundance.
ISSN:1043-4666
1096-0023
DOI:10.1016/j.cyto.2008.06.004