Upregulation of hepcidin by interleukin-1beta in human hepatoma cell lines. |
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Authors: | Junki Inamura Katsuya Ikuta Junko Jimbo Motohiro Shindo Kazuya Sato Yoshihiro Torimoto Yutaka Kohgo |
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Affiliation: | Third Department of Internal Medicine, Asahikawa Medical College, 2-1-1-1 Midorigaoka-Higashi, Asahikawa, Hokkaido 078-8510, Japan. |
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Abstract: | Anemia of chronic disease (ACD) is commonly observed in chronic inflammation, although its pathogenesis is poorly understood. Hepcidin is thought to be a key regulator in iron metabolism and has been implicated in ACD. Although the induction of hepcidin by an inflammatory cytokine interleukin-6 (IL-6) seems to have been confirmed, it is still controversial whether interleukin-1beta (IL-1beta), also known as an inflammatory cytokine, regulates hepcidin expression. We demonstrated that hepcidin mRNA was upregulated by IL-1beta in human hepatoma-derived HuH-7 cells, particularly at low concentrations of IL-1beta, while high concentrations of IL-6 were needed for the upregulation of hepcidin mRNA. Therefore, IL-1beta might be more important for the upregulation of hepcidin in physiological conditions than IL-6. Although IL-1beta induces IL-6 production in hepatocytes, our data indicate that the effect of IL-1beta on hepcidin expression is independent from that of IL-6. In conclusion, IL-1beta might have an important role in ACD. |
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Keywords: | Hepcidin Anemia of chronic disease (ACD) Interleukin-1β (IL-1β) Interleukin-6 (IL-6) Iron metabolism HuH-7 cells |
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