Kim Hyeon Ho, Lee Youngae, Eun Hee Chul, Chung Jin Ho
Department of Dermatology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Biochem Biophys Res Commun. 2008 Apr 4;368(2):343-9. doi: 10.1016/j.bbrc.2008.01.062. Epub 2008 Jan 28.
Eicosapentaenoic acid (EPA) is an omega-3 (omega-3) polyunsaturated fatty acid (PUFA), which has anti-inflammatory and anti-cancer properties. Some reports have demonstrated that EPA inhibits NF-kappaB activation induced by tumor necrosis factor (TNF)-alpha or lipopolysaccharide (LPS) in various cells. However, its detailed mode of action is unclear. In this report, we investigated whether EPA inhibits the expression of TNF-alpha-induced matrix metalloproteinases (MMP)-9 in human immortalized keratinocytes (HaCaT). TNF-alpha induced MMP-9 expression by NF-kappaB-dependent pathway. Pretreatment of EPA inhibited TNF-alpha-induced MMP-9 expression and p65 phosphorylation. However, EPA could not affect IkappaB-alpha phosphorylation, nuclear translocation of p65, and DNA binding activity of NF-kappaB. EPA inhibited TNF-alpha-induced p65 phosphorylation through p38 and Akt inhibition and this inhibition was IKKalpha-dependent event. Taken together, we demonstrate that EPA inhibits TNF-alpha-induced MMP-9 expression through inhibition of p38 and Akt activation.
二十碳五烯酸(EPA)是一种ω-3多不饱和脂肪酸(PUFA),具有抗炎和抗癌特性。一些报告表明,EPA可抑制肿瘤坏死因子(TNF)-α或脂多糖(LPS)在各种细胞中诱导的核因子-κB(NF-κB)激活。然而,其具体作用方式尚不清楚。在本报告中,我们研究了EPA是否抑制人永生化角质形成细胞(HaCaT)中TNF-α诱导的基质金属蛋白酶(MMP)-9的表达。TNF-α通过NF-κB依赖途径诱导MMP-9表达。EPA预处理可抑制TNF-α诱导的MMP-9表达和p65磷酸化。然而,EPA不影响IκB-α磷酸化、p65核转位以及NF-κB的DNA结合活性。EPA通过抑制p38和Akt抑制TNF-α诱导的p65磷酸化,且这种抑制是依赖IKKα的事件。综上所述,我们证明EPA通过抑制p38和Akt激活来抑制TNF-α诱导的MMP-9表达。