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铁状态和脂多糖通过激活核因子-κB来调节Ndfip1。

Iron status and lipopolysaccharide regulate Ndfip1 by activation of nuclear factor-kappa B.

作者信息

Xu Huamin, Chang Qing, Jia Wenting, Jiang Hong, Sun Peng, Xie Junxia

机构信息

Department of Physiology, Shandong Provincial Key Laboratory of Pathogenesis and Prevention of Neurological Disorders and State Key Disciplines: Physiology, Medical College of Qingdao University, No. 308 Ningxia Road, Qingdao, 266071, China.

出版信息

Biometals. 2013 Dec;26(6):981-8. doi: 10.1007/s10534-013-9674-7. Epub 2013 Sep 18.

Abstract

Nedd4 family interacting protein 1 (Ndfip1) is an adaptor protein for the Nedd4 family of ubiquitin ligases that target proteins for degradation. Recent studies confirmed the role of Ndfip1 as a regulator of iron metabolism and pointed out that Ndfip1 was involved in iron homeostasis by regulating the degradation of iron importer divalent metal transporter 1 (DMT1). However, little is known about how Ndfip1 is regulated. The aim of this article was to investigate the regulation of Ndfip1 levels and the possible mechanisms. In this study, we investigated the effect of various stimuli, including iron status and lipopolysaccharide (LPS) on Ndfip1 expression in MES23.5 dopaminergic cell lines. Results showed that Ndfip1 expression in these cells was enhanced by ferrous iron overload, but not ferric iron overload, and decreased after iron deprivation by deferoxamine. In addition, LPS could significantly increase the expression of Ndfip1. Furthermore, we demonstrated that the regulation of Ndfip1 expression by these various stimuli was achieving by activation of nuclear factor-kappa B. We speculate that iron status and LPS may contribute to the changes of Ndfip1 expression by activation of nuclear factor-kappa B.

摘要

Nedd4家族相互作用蛋白1(Ndfip1)是一种衔接蛋白,用于泛素连接酶的Nedd4家族,该家族将蛋白质靶向降解。最近的研究证实了Ndfip1作为铁代谢调节剂的作用,并指出Ndfip1通过调节铁输入蛋白二价金属转运体1(DMT1)的降解参与铁稳态。然而,关于Ndfip1如何被调节知之甚少。本文的目的是研究Ndfip1水平的调节及其可能的机制。在本研究中,我们研究了包括铁状态和脂多糖(LPS)在内的各种刺激对MES23.5多巴胺能细胞系中Ndfip1表达的影响。结果表明,亚铁过载而非高铁过载可增强这些细胞中Ndfip1的表达,而去铁胺剥夺铁后Ndfip1表达降低。此外,LPS可显著增加Ndfip1的表达。此外,我们证明了这些各种刺激对Ndfip1表达的调节是通过激活核因子-κB实现的。我们推测铁状态和LPS可能通过激活核因子-κB导致Ndfip1表达的变化。

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