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Alpinetin enhances cholesterol efflux and inhibits lipid accumulation in oxidized low-density lipoprotein-loaded human macrophages

机译:Alpinetin增强胆固醇流出并抑制氧化的低密度脂蛋白载人巨噬细胞中的脂质蓄积

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Alpinetin is a natural flavonoid abundantly present in the ginger family. Here, we investigated the effect of alpinetin on cholesterol efflux and lipid accumulation in oxidized low-density lipoprotein (ox-LDL)-treated THP-1 macrophages and human peripheral blood monocyte-derived macrophages (HMDMs). After exposing THP-1 macrophages to alpinetin, cholesterol efflux was determined by liquid scintillator. The mRNA and protein levels of peroxisome proliferator-activated receptor gamma (PPAR-), liver X receptor alpha (LXR-), ATP-binding cassette transporter A1 (ABCA1), and ABCG1 and scavenger receptor class B member 1 were determined by reverse-transcriptase PCR (RT-PCR) and Western blot analysis, respectively. Alpinetin promoted apolipoprotein A-I- and high-density-lipoprotein-mediated cholesterol efflux and elevated PPAR- and LXR- mRNA and protein expression in a dose-dependent fashion in ox-LDL-treated THP-1 macrophages and HMDMs. Small interfering RNA-mediated silencing of PPAR- or LXR- dose dependently reversed alpinetin-increased cholesterol efflux in THP-1 macrophages, indicating the involvement of PPAR- and LXR- in alpinetin-promoted cholesterol efflux. Alpinetin inhibited ox-LDL-induced lipid accumulation and enhanced the expression of ABCA1 and ABCG1 mRNA and protein, which was reversed by specific knockdown of PPAR- or LXR-. Taken together, our results reveal that alpinetin exhibits positive effects on cholesterol efflux and inhibits ox-LDL-induced lipid accumulation, which might be through PPAR-/LXR-/ABCA1/ABCG1 pathway. (C) 2014 International Union of Biochemistry and Molecular Biology, Inc.
机译:Alpinetin是姜家族中大量存在的天然类黄酮。在这里,我们研究了高铁素对氧化低密度脂蛋白(ox-LDL)处理的THP-1巨噬细胞和人外周血单核细胞衍生的巨噬细胞(HMDM)中胆固醇外流和脂质蓄积的影响。将THP-1巨噬细胞暴露于高铁素后,通过液体闪烁器测定胆固醇外流。过氧化物酶体增殖物激活受体γ(PPAR-),肝X受体α(LXR-),ATP结合盒转运蛋白A1(ABCA1)以及ABCG1和清除剂受体B类成员1的mRNA和蛋白水平通过反向-转录酶PCR(RT-PCR)和蛋白质印迹分析。 Alpinetin在经ox-LDL处理的THP-1巨噬细胞和HMDM中以剂量依赖的方式促进载脂蛋白A-I和高密度脂蛋白介导的胆固醇外流,并升高PPAR-和LXR-mRNA和蛋白表达。 RNA介导的PPAR或LXR-的小干扰沉默可逆转THP-1巨噬细胞中增加的alpinetin增加的胆固醇流出,表明PPAR-和LXR-参与altintin促进的胆固醇流出。 Alpinetin抑制ox-LDL诱导的脂质蓄积并增强ABCA1和ABCG1 mRNA和蛋白质的表达,这可以通过特异性敲除PPAR-或LXR-来逆转。两者合计,我们的结果表明,高铁素对胆固醇外流具有积极作用,并抑制ox-LDL诱导的脂质蓄积,这可能是通过PPAR- / LXR- / ABCA1 / ABCG1途径引起的。 (C)2014国际生物化学与分子生物学联合会

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