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首页> 外文期刊>The Journal of Nutritional Biochemistry >The iron regulatory hormone hepcidin inhibits expression of iron release as well as iron uptake proteins in J774 cells
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The iron regulatory hormone hepcidin inhibits expression of iron release as well as iron uptake proteins in J774 cells

机译:铁调节激素铁调素抑制J774细胞中铁释放以及铁摄取蛋白的表达

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摘要

The mechanism by which hepcidin controls cellular iron release protein ferroportin 1 (Fpn1) in macrophages has been well established. However, little is known about the effects of hepcidin on cellular iron uptake proteins. Here, we demonstrated for the first time that hepcidin can significantly inhibit the expression of transferrin receptor 1 (TfR1) and divalent metal transporter 1 in addition to Fpn1, and therefore reduce transferrin-bound iron and non-transferrin-bound iron uptake and also iron release in J774 macrophages. Analysis of mechanisms using the iron-depleted cells showed that hepcidin has a direct inhibitory effect on all iron transport proteins we examined. Further studies demonstrated that the down-regulation of TfR1 induced by hepcidin is associated with cyclic adenosine monophosphate (cAMP) and protein kinase A (PKA), probably being mediated by the cAMP–PKA pathway in J774 macrophages.
机译:hepcidin控制巨噬细胞中的细胞铁释放蛋白ferroportin 1(Fpn1)的机制已经建立。然而,关于铁调素对细胞铁摄取蛋白的影响知之甚少。在这里,我们首次证明铁调素可以显着抑制除Fpn1之外的转铁蛋白受体1(TfR1)和二价金属转运蛋白1的表达,从而减少与转铁蛋白结合的铁和未与转铁蛋白结合的铁的摄取,以及铁在J774巨噬细胞中释放。使用贫铁细胞的机制分析表明,铁调素对我们研究的所有铁转运蛋白都有直接的抑制作用。进一步的研究表明,铁调素诱导的TfR1的下调与环状单磷酸腺苷(cAMP)和蛋白激酶A(PKA)相关,可能是由J774巨噬细胞中的cAMP–PKA途径介导的。

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