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CYP2J2 overexpression increases EETs and protects against angiotensin II-induced abdominal aortic aneurysm in mice

机译:CYP2J2过表达增加EET并保护小鼠免受血管紧张素II诱导的腹主动脉瘤

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摘要

Cytochrome P450 epoxygenase 2J2 (CYP2J2) metabolizes arachidonic acids to form epoxyeicosatrienoic acids (EETs), which possess various beneficial effects on the cardiovascular system. However, whether increasing EETs production by CYP2J2 overexpression in vivo could prevent abdominal aortic aneurysm (AAA) remains unknown. Here we investigated the effects of recombinant adeno-associated virus (rAAV)-mediated CYP2J2 overexpression on angiotensin (Ang) II-induced AAA in apoE-deficient mice. rAAV-CYP2J2 delivery led to an abundant aortic CYP2J2 expression and increased EETs generation. It was shown that CYP2J2 overexpression attenuated matrix metalloproteinase expression and activity, elastin degradation, and AAA formation, which was associated with reduced aortic inflammation and macrophage infiltration. In cultured vascular smooth muscle cells (VSMCs), rAAV-mediated CYP2J2 overexpression and EETs markedly suppressed Ang II-induced inflammatory cytokine expression. Moreover, overexpressed CYP2J2 and EETs inhibited Ang II-induced macrophage migration in a VSMC-macrophage coculture system. We further indicated that these protective effects were mediated by peroxisome proliferator-activated receptor (PPAR)γ activation. Taken together, these results provide evidence that rAAV-mediated CYP2J2 overexpression prevents AAA development which is likely via PPARγ activation and anti-inflammatory action, suggesting that increasing EETs levels could be considered as a potential strategy to prevent and treat AAA.
机译:细胞色素P450环氧合酶2J2(CYP2J2)代谢花生四烯酸形成环氧二十碳三烯酸(EET),对心血管系统具有多种有益作用。但是,是否通过CYP2J2的体内过表达增加EETs的产生是否可以预防腹主动脉瘤(AAA),仍然是未知的。在这里,我们研究了重组腺相关病毒(rAAV)介导的CYP2J2过表达对apoE缺陷小鼠中血管紧张素(Ang)II诱导的AAA的影响。 rAAV-CYP2J2传递导致丰富的主动脉CYP2J2表达并增加EET的产生。结果表明,CYP2J2的过表达会减弱基质金属蛋白酶的表达和活性,弹性蛋白降解以及AAA形成,这与减少主动脉炎症和巨噬细胞浸润有关。在培养的血管平滑肌细胞(VSMC)中,rAAV介导的CYP2J2过表达和EETs显着抑制了Ang II诱导的炎性细胞因子表达。此外,在VSMC-巨噬细胞共培养系统中,CYP2J2和EETs的过表达抑制了Ang II诱导的巨噬细胞迁移。我们进一步表明,这些保护作用是由过氧化物酶体增殖物激活受体(PPAR)γ激活介导的。综上所述,这些结果提供了证据,证明rAAV介导的CYP2J2过表达阻止了AAA的发展,这很可能是通过PPARγ激活和抗炎作用而来的,这表明增加EETs水平可被视为预防和治疗AAA的潜在策略。

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