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Impaired transactivation of the human CYP2J2 arachidonic acid epoxygenase gene in HepG2 cells subjected to nitrative stress
Author(s) -
Cui Pei H,
Lee Andy C,
Zhou Fanfan,
Murray Michael
Publication year - 2010
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2009.00628.x
Subject(s) - kinase , epoxygenase , p38 mitogen activated protein kinases , protein kinase a , mapk/erk pathway , activator (genetics) , microbiology and biotechnology , biology , cytochrome p450 , chemistry , biochemistry , gene , enzyme
Background and purpose: Human cytochrome P450 2J2 (CYP2J2) generates epoxyfatty acids that modulate cellular apoptosis and proliferation. CYP2J2 regulation has not been intensively studied but induction of the activator protein‐1 (AP‐1) subunit c‐fos mediates CYP2J2 down‐regulation in hypoxia, a component of ischaemic injury. Decreased CYP2J2 expression may contribute to tissue injury. Experimental approach: HepG2 cells were treated with sodium nitroprusside (SNP) to induce nitrative stress, which has been associated with inflammation and infection in liver and other tissues. CYP2J2 protein and mRNA expression were evaluated by immunoblotting and real‐time PCR respectively. The role of mitogen‐activated protein (MAP) kinases in CYP2J2 dysregulation was assessed using specific inhibitors and dominant negative MAP kinase expression plasmids. CYP2J2‐luciferase reporter constructs and electromobility shift assays (EMSAs) were used to identify SNP‐regulated regions in the CYP2J2 gene. Key results: Cytochrome P450 2J2 was down‐regulated by SNP while the AP‐1 proteins c‐jun and c‐fos were up‐regulated; inhibition of p38 and ERK MAP kinases normalized their expression. The gene elements at −105/−95 and −56/−63 were required for the down‐regulation of CYP2J2 induced by nitrative stress. Conclusions and implications: p38 and ERK MAP kinases transduce stress stimuli that down‐regulate CYP2J2. Targeting these kinases may prevent the loss of CYP2J2 and epoxy‐fatty acids that protect cells against deleterious stresses.