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山楂酸调节分泌型磷脂酶A2-IIA(sPLA2-IIA)介导的巨噬细胞泡沫细胞形成中的炎症效应。

Maslinic acid modulates secreted phospholipase A2-IIA (sPLA2-IIA)-mediated inflammatory effects in macrophage foam cells formation.

作者信息

Yap Wei Hsum, Ooi Bee Kee, Ahmed Nafees, Lim Yang Mooi

机构信息

School of Biosciences, Taylor's University, Subang Jaya, Selangor, Malaysia.

出版信息

J Biosci. 2018 Jun;43(2):277-285.

Abstract

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.

摘要

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。

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