Lead induces dysregulation of iron regulatory protein 1 via the extracellular signal-regulated kinase pathway in human vascular endothelial cells

被引:10
作者
Wang, Qiang [1 ,2 ,3 ]
Lin, Yan [4 ]
Zhang, Wenbin [1 ,2 ]
Liu, Mingchao [1 ,2 ]
Chen, Yaoming [1 ,2 ]
Chen, Jingyuan [1 ,2 ]
Luo, Wenjing [1 ,2 ]
机构
[1] Fourth Mil Med Univ, Sch Publ Hlth, Dept Occupat & Environm Hlth, Xian 710032, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Sch Publ Hlth, Minist Educ, Key Lab Hazard Assessment & Control Special Opera, Xian 710032, Shaanxi, Peoples R China
[3] Acad Mil Med Sci, Inst Dis Prevent & Control, Beijing 100071, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Ophthalmol, Xian 710032, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Lead; Iron; Vascular endothelium; Iron regulatory protein 1; ERK pathway; INDUCED HYPERTENSION; MOLECULAR CONTROL; DEPENDENT DEGRADATION; OXIDATIVE STRESS; DOWN-REGULATION; NITRIC-OXIDE; METABOLISM; PHOSPHORYLATION; SUPEROXIDE; ACTIVATION;
D O I
10.1016/j.brainres.2012.03.052
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Lead (Pb) can target the vascular system for both acute injury and disease promotion. Cellular iron (Fe) disruption may be implicated in Pb vascular toxicity. To investigate the potential involvement of iron response element 1 (IRP1) protein in the vascular endothelium during Pb exposure, human umbilical vein endothelial cells (HUVEC) were treated with different concentrations of lead nitrate, 30 mu M iron sulfate, or 100 mu M deferoxamine. PD98059, a specific inhibitor of the mitogen-activated protein kinase kinase (MEK) activator, was administered to block the ERK/MAPK pathway. Western blotting was used to detect the expression of IRP1 and p-ERK1/2, and microscopy, and co-immunoprecipitation was used to show the association between IRP1 and p-ERK1/2. In vitro measurements revealed a decrease in IRP1 and activated ERK1/2 in the membrane following Pb treatment. HUVEC treated with PD98059 enhanced the levels of membrane IRP1 and efficiently inhibited the effect of Pb on the levels of membrane IRP1. Partial IRP1 co-localization existed with p-ERK1/2 in the membrane, and Pb treatment produced an obvious decrease in the amount of IRP1 that co-localized with pERK1/2. Co-immunoprecipitation further revealed a possible association between IRP-1 and p-ERK1/2. Collectively, Pb specifically induced the dysregulation of IRP1 protein by activating the ERK1/2 signaling pathway in the plasma membrane, indicating a novel role for IRP1 and the ERK/MAPK pathway in vascular endothelial functions. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 27
页数:9
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