6-Hydroxydopamine upregulates iron regulatory protein 1 by activating certain protein kinase C isoforms in the dopaminergic MES23.5 cell line

被引:7
作者
Wang, Wenjie
Song, Ning
Zhang, Haoyun
Xie, Junxia
Wang, Jun [1 ]
机构
[1] Qingdao Univ, Dept Physiol, Shandong Prov Key Lab Pathogenesis & Prevent Neur, Coll Med, Qingdao 266071, Peoples R China
基金
中国国家自然科学基金;
关键词
Parkinson's disease; Iron; Ferroportin; 1; Iron regulatory protein 1; Protein kinase C; 6-Hydroxydopamine; PARKINSONS-DISEASE; INDUCED APOPTOSIS; NITRIC-OXIDE; PKC-ZETA; IN-VIVO; KAPPA-B; ACCUMULATION; EXPRESSION; BINDING; METABOLISM;
D O I
10.1016/j.biocel.2012.07.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Iron-induced oxidative stress is thought to play a crucial role in the pathogenesis of Parkinson's disease. Our previous studies demonstrated that decreased expression of ferroportin 1 contributes to 6-hydroxydopamine induced intracellular iron accumulation and that decreased ferroportin 1 expression is caused by increased expression of iron regulatory protein 1. Iron regulatory protein 1 is a central regulator of iron homeostasis and is a likely target of extracellular agents to program changes in cellular iron metabolism. Therefore, the mechanism of iron regulatory protein 1 upregulation induced by 6-hydroxydopamine has become a significant focus of research. Iron regulatory protein 1 is regulated by protein kinase C, although this regulation is tissue specific. Therefore, in the present study, we aimed to determine whether alteration of protein kinase C activity modified iron regulatory protein 1 expression in the dopaminergic MES23.5 cell line, Furthermore, we investigated whether 6-hydroxydopamine induced iron regulatory protein 1 upregulation is mediated by protein kinase C, thus achieving regulation of cellular iron levels. The results showed that iron regulatory protein 1 was upregulated by phorbol 12-myristate-13-acetate, the PKC activator in dopaminergic MES23.5 cells, and ferroportin 1 expression and iron efflux were decreased as a result of iron regulatory protein 1 upregulation. The protein kinase C inhibitor bisindolylmaleimide I hydrochloride abolished the effect of phorbol 12-myristate-13-acetate. Protein kinase C-delta and protein kinase C-zeta, but not protein kinase C-epsilon were activated by 6-hydroxydopamine. The protein kinase C-delta inhibitor rottlerin inhibited protein kinase C-delta phosphorylation and abolished iron regulatory protein 1 upregulation induced by 6-hydroxydopamine. The protein kinase C-zeta pseudo-substrate inhibitor inhibited protein kinase C-zeta phosphorylation and abolished iron regulatory protein I upregulation induced by 6-hydroxydopamine. These data indicate that iron regulatory protein 1 is regulated by protein kinase C in dopaminergic MES23.5 cells and that protein kinase C activated by 6-hydroxydopamine regulates iron regulatory protein 1 expression, thus achieving regulation of cellular iron levels. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1987 / 1992
页数:6
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