Upregulation of hepcidin by interleukin-1β in human hepatoma cell lines

被引:36
作者
Inamura, J [1 ]
Ikuta, K [1 ]
Jimbo, J [1 ]
Shindo, M [1 ]
Sato, K [1 ]
Torimoto, Y [1 ]
Kohgo, Y [1 ]
机构
[1] Asahikawa Med Coll, Dept Internal Med 3, Asahikawa, Hokkaido 0788510, Japan
关键词
hepcidin; anemia of chronic disease (ACD); interleukin-1 beta (1L-1 beta); interleukin-6 (IL-6); iron metabolism; HuH-7; cells;
D O I
10.1016/j.hepres.2005.08.005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 AM Although the induction of hepcidin by an inflammatory cytokine interleukin-6 (IL-6) seems to have been confirmed, it is still controversial whether interleukin-1 beta (IL-1 beta), also known as an inflammatory cytokine, regulates hepcidin expression. We demonstrated that hepcidin mRNA was upregulated by IL-1 beta in human hepatoma-derived HuH-7 cells, particularly at low concentrations of IL-1 beta, while high concentrations of IL-6 were needed for the upregulation of hepcidin mRNA. Therefore, IL-1 beta might be more important for the upregulation of hepcidin in physiological conditions than IL-6. Although IL-1 beta induces IL-6 production in hepatocytes, our data indicate that the effect of IL-1 beta on hepcidin expression is independent from that of IL-6. In conclusion, IL-1 beta might have an important role in ACD. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:198 / 205
页数:8
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