Yap Wei Hsum, Ooi Bee Kee, Ahmed Nafees, Lim Yang Mooi
School of Biosciences, Taylor's University, Subang Jaya, Selangor, Malaysia.
J Biosci. 2018 Jun;43(2):277-285.
Secretory phospholipase A2-IIA (sPLA2-IIA) is one of the key enzymes causing lipoprotein modification and vascular inflammation. Maslinic acid is a pentacyclic triterpene which has potential cardioprotective and anti-inflammatory properties. Recent research showed that maslinic acid interacts with sPLA2-IIA and inhibits sPLA2-IIA-mediated monocyte differentiation and migration. This study elucidates the potential of maslinic acid in modulating sPLA2-IIA-mediated inflammatory effects in THP-1 macrophages. We showed that maslinic acid inhibits sPLA2-IIA-mediated LDL modification and suppressed foam cell formation. Further analysis revealed that sPLA2-IIA only induced modest LDL oxidation and that inhibitory effect of maslinic acid on sPLA2-IIA-mediated foam cells formation occurred independently of its anti-oxidative properties. Interestingly, maslinic acid was also found to significantly reduce lipid accumulation observed in macrophages treated with sPLA2-IIA only. Flow cytometry analysis demonstrated that the effect observed in maslinic acid might be contributed in part by suppressing sPLA2-IIA-induced endocytic activity, thereby inhibiting LDL uptake. The study further showed that maslinic acid suppresses sPLA2-IIA-induced up-regulation of PGE2 levels while having no effects on COX-2 activity. Other pro-inflammatory mediators TNF-a and IL-6 were not induced in sPLA2-IIA-treated THP-1 macrophages. The findings of this study showed that maslinic acid inhibit inflammatory effects induced by sPLA2-IIA, including foam cells formation and PGE2 production.
分泌型磷脂酶A2-IIA(sPLA2-IIA)是导致脂蛋白修饰和血管炎症的关键酶之一。山楂酸是一种五环三萜,具有潜在的心脏保护和抗炎特性。最近的研究表明,山楂酸与sPLA2-IIA相互作用,并抑制sPLA2-IIA介导的单核细胞分化和迁移。本研究阐明了山楂酸在调节THP-1巨噬细胞中sPLA2-IIA介导的炎症效应方面的潜力。我们发现山楂酸抑制sPLA2-IIA介导的低密度脂蛋白(LDL)修饰,并抑制泡沫细胞形成。进一步分析表明,sPLA2-IIA仅诱导适度的LDL氧化,且山楂酸对sPLA2-IIA介导的泡沫细胞形成的抑制作用与其抗氧化特性无关。有趣的是,还发现山楂酸能显著减少仅用sPLA2-IIA处理的巨噬细胞中观察到的脂质积累。流式细胞术分析表明,山楂酸观察到的效应可能部分是通过抑制sPLA2-IIA诱导的内吞活性,从而抑制LDL摄取。该研究还表明,山楂酸抑制sPLA2-IIA诱导的前列腺素E2(PGE2)水平上调,而对环氧合酶-2(COX-2)活性无影响。在用sPLA2-IIA处理的THP-1巨噬细胞中未诱导其他促炎介质肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)。本研究结果表明,山楂酸抑制sPLA2-IIA诱导的炎症效应,包括泡沫细胞形成和PGE2产生。