Cargando…

Nrf2(−/−) regulated lung DNA demethylation and CYP2E1 DNA methylation under PM(2.5) exposure

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) e...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Mengjie, Jiang, Menghui, Ding, Hao, Tang, Siying, Li, Daochuan, Pi, Jingbo, Zhang, Rong, Chen, Wen, Chen, Rui, Zheng, Yuxin, Piao, Jinmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10128193/
https://www.ncbi.nlm.nih.gov/pubmed/37113990
http://dx.doi.org/10.3389/fgene.2023.1144903
Descripción
Sumario: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).