Activation of EGFR/MEK/ERK/AP-1 signaling mediated by 1,2-naphthoquinone, an atmospheric electrophile, in human pulmonary A549 cells

被引:0
|
作者
Beei, Chang [1 ]
Iwamoto, Noriko [2 ]
Inaba, Takako [1 ]
Shinkai, Yasuhiro [1 ,2 ]
Kumagai, Yoshito [1 ,2 ]
机构
[1] Univ Tsukuba, Grad Sch Life & Environm Sci, Masters Program Environm, Tsukuba, Ibaraki 3058575, Japan
[2] Univ Tsukuba, Grad Sch Comprehens Human Sci, Doctoral Program Biomed Sci, Tsukuba, Ibaraki 3058575, Japan
来源
JOURNAL OF TOXICOLOGICAL SCIENCES | 2013年 / 38卷 / 05期
关键词
Electrophile; Covalent modification; Signal transduction; EGFR; GROWTH-FACTOR RECEPTOR; KINASE; INHIBITOR; PROTEINS;
D O I
暂无
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1,2-Naphthoquinone (1,2-NQ) is found to be an electrophile contaminated in the atmosphere. Although we found that 1,2-NQ activates epidermal growth factor receptor (EGFR) coupled to inhibition of protein tyrosine phosphatase 1B (PTP1B) activity through covalent modification of Cys121 in human epithelial A431 cells, modulation of its downstream signal transduction pathway caused by 1,2-NQ remains to be elucidated In the present study, we examined whether 1,2-NQ could affect such cellular signaling in human pulmonary A549 cells. Exposure of A549 cells to 1,2-NQ increased EGFR phosphorylation, resulting in activation of MEK/ERK signaling that was blocked by either PD15035 or PD98059. As a result, DNA binding activity of transcription factor AP-1 was enhanced during exposure to 1,2-NQ in the cells. These results suggest that the atmospheric electrophile phosphorylates EGFR, thereby activating the MEK/ERK/AP-1 signal transduction pathway in A549 cells.
引用
收藏
页码:793 / 797
页数:5
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