Prostaglandin E2 increases fibroblast gene-specific and global DNA methylation via increased DNA methyltransferase expression

被引:47
|
作者
Huang, Steven K. [1 ]
Scruggs, Anne M. [1 ]
Donaghy, Jake [1 ]
McEachin, Richard C. [2 ]
Fisher, Aaron S. [1 ]
Richardson, Bruce C. [3 ]
Peters-Golden, Marc [1 ]
机构
[1] Univ Michigan, Sch Med, Div Pulm & Crit Care Med, Ann Arbor, MI USA
[2] Univ Michigan, Sch Med, Dept Computat Med & Bioinformat, Ann Arbor, MI USA
[3] Univ Michigan, Sch Med, Div Rheumatol, Ann Arbor, MI USA
来源
FASEB JOURNAL | 2012年 / 26卷 / 09期
基金
美国国家卫生研究院;
关键词
epigenetics; eicosanoids; macrophage; RECEPTOR-MEDIATED INCREASE; LUNG FIBROBLASTS; E-PROSTANOID-2; RECEPTOR; DE-NOVO; TRANSCRIPTIONAL REGULATION; INHIBITS FIBROBLAST; MAMMALIAN-CELLS; CANCER; GROWTH; CYCLOOXYGENASE-2;
D O I
10.1096/fj.11-203323
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
Although alterations in DNA methylation patterns have been associated with specific diseases and environmental exposures, the mediators and signaling pathways that direct these changes remain understudied. The bioactive lipid mediator prostaglandin E-2 (PGE(2)) has been shown to exert a myriad of effects on cell survival, proliferation, and differentiation. Here, we report that PGE(2) also signals to increase global DNA methylation and DNA methylation machinery in fibroblasts. HumanMethylation27 BeadChip array analysis of primary fetal (IMR-90) and adult lung fibroblasts identified multiple genes that were hypermethylated in response to PGE(2). PGE(2), compared with nontreated controls, increased expression and activity (EC50 similar to 10(7) M) of one specific isoform of DNA methyltransferase, DNMT3a. Silencing of DNMT3a negated the ability of PGE(2) to increase DNMT activity. The increase in DNMT3a expression was mediated by PGE(2) signaling via its E prostanoid 2 receptor and the second messenger cAMP. PGE(2), compared with the untreated control, increased the expression and activity of Sp1 and Sp3 (EC50 similar to 3 x 10(7) M), transcription factors known to increase DNMT3a expression, and inhibition of these transcription factors abrogated the PGE(2) increase of DNMT3a expression. These findings were specific to fibroblasts, as PGE(2) decreased DNMT1 and DNMT3a expression in RAW macrophages. Taken together, these findings establish that DNA methylation is regulated by a ubiquitous bioactive endogenous mediator. Given that PGE(2) biosynthesis is modulated by environmental toxins, various disease states, and commonly used pharmacological agents, these findings uncover a novel mechanism by which alterations in DNA methylation patterns may arise in association with disease and certain environmental exposures.-Huang, S. K., Scruggs, A. M., Donaghy, J., McEachin, R. C., Fisher, A. S., Richardson, B. C., Peters-Golden, M. Prostaglandin E-2 increases fibroblast gene-specific and global DNA methylation via increased DNA methyltransferase expression. FASEB J. 26, 3703-3714 (2012). www.fasebj.org
引用
收藏
页码:3703 / 3714
页数:12
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