Nrf2-/- regulated lung DNA demethylation and CYP2E1 DNA methylation under PM2.5 exposure

Mengjie Wu; Menghui Jiang; Hao Ding; Siying Tang; Daochuan Li; Jingbo Pi; Rong Zhang; Wen Chen; Rui Chen; Yuxin Zheng; Jinmei Piao

doi:10.3389/fgene.2023.1144903

Nrf2^-/- regulated lung DNA demethylation and CYP2E1 DNA methylation under PM_2.5 exposure

Front Genet. 2023 Mar 20:14:1144903. doi: 10.3389/fgene.2023.1144903. eCollection 2023.

Authors

Mengjie Wu¹, Menghui Jiang¹, Hao Ding², Siying Tang³, Daochuan Li⁴, Jingbo Pi⁵, Rong Zhang⁶, Wen Chen⁴, Rui Chen⁷, Yuxin Zheng¹, Jinmei Piao¹

Affiliations

¹ School of Public Health, Qingdao University, Qingdao, China.
² The Municipal Government Hospital of Zibo, Zibo, Shandong, China.
³ Qingdao Chengyang District Center for Disease Control and Prevention, Qingdao, China.
⁴ Department of Toxicology, School of Public Health, Sun Yat-Sen University, Guangzhou, China.
⁵ School of Public Health, China Medical University, Shenyang, China.
⁶ Department of Toxicology, School of Public Health, Hebei Medical University, Shijiazhuang, China.
⁷ School of Public Health, Capital Medical University, Beijing, China.

Abstract

Cytochrome P450 (CYP450) can mediate fine particulate matter (PM_2.5) exposure leading to lung injury. Nuclear factor E2-related factor 2 (Nrf2) can regulate CYP450 expression; however, the mechanism by which Nrf2^-/- (KO) regulates CYP450 expression via methylation of its promoter after PM_2.5 exposure remains unclear. Here, Nrf2^-/- (KO) mice and wild-type (WT) were placed in a PM_2.5 exposure chamber (PM) or a filtered air chamber (FA) for 12 weeks using the real-ambient exposure system. The CYP2E1 expression trends were opposite between the WT and KO mice following PM_2.5 exposure. After exposure to PM_2.5, CYP2E1 mRNA and protein levels were increased in WT mice but decreased in KO mice, and CYP1A1 expression was increased after exposure to PM_2.5 in both WT and KO mice. CYP2S1 expression decreased after exposure to PM_2.5 in both the WT and KO groups. We studied the effect of PM_2.5 exposure on CYP450 promoter methylation and global methylation levels in WT and KO mice. In WT and KO mice in the PM_2.5 exposure chamber, among the methylation sites examined in the CYP2E1 promoter, the CpG2 methylation level showed an opposite trend with CYP2E1 mRNA expression. The same relationship was evident between CpG3 unit methylation in the CYP1A1 promoter and CYP1A1 mRNA expression, and between CpG1 unit methylation in the CYP2S1 promoter and CYP2S1 mRNA expression. This data suggests that methylation of these CpG units regulates the expression of the corresponding gene. After exposure to PM_2.5, the expression of the DNA methylation markers ten-eleven translocation 3 (TET3) and 5-hydroxymethylcytosine (5hmC) was decreased in the WT group but significantly increased in the KO group. In summary, the changes in CYP2E1, CYP1A1, and CYP2S1 expression in the PM_2.5 exposure chamber of WT and Nrf2^-/- mice might be related to the specific methylation patterns in their promoter CpG units. After exposure to PM_2.5, Nrf2 might regulate CYP2E1 expression by affecting CpG2 unit methylation and induce DNA demethylation via TET3 expression. Our study revealed the underlying mechanism for Nrf2 to regulate epigenetics after lung exposure to PM_2.5.

Keywords: CYP2E1; DNA methylation; Nrf2; PM2.5; Tet3.

Grants and funding

This study was primarily supported by the National Natural Science Foundation of China (Nos. 81872600, 91943301), and the Natural Science Foundation of Shandong Province, China (No. ZR2020MH333), and the Guangdong Provincial Natural Science Foundation Team Project (2018B030312005).