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首页> 外文期刊>Marine Drugs >The Anti-Inflammatory Effect and Structure of EPCP1-2 from Crypthecodinium cohnii via Modulation of TLR4-NF-???oB Pathways in LPS-Induced RAW 264.7 Cells
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The Anti-Inflammatory Effect and Structure of EPCP1-2 from Crypthecodinium cohnii via Modulation of TLR4-NF-???oB Pathways in LPS-Induced RAW 264.7 Cells

机译:脂多糖诱导的LP 26诱导的RAW 264.7细胞中TLR4-NF-βoB途径对Crypthecodinium cohnii EPCP1-2的抗炎作用和结构

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Exopolysaccharide from Crypthecodinium cohnii (EPCP1-2) is a marine exopolysaccharide that evidences a variety of biological activities. We isolated a neutral polysaccharide from the fermentation liquid of Crypthecodinium cohnii (CP). In this study, a polysaccharide that is derived from Crypthecodinium cohnii were analyzed and its anti-inflammatory effect was evaluated on protein expression of toll-like receptor 4 and nuclear factor ???oB pathways in macrophages. The structural characteristics of EPCP1-2 were characterized by GC (gas chromatography) and GC-MS (gas Chromatography-Mass Spectrometer) analyses. The molecular weight was about 82.5 kDa. The main chain of EPCP1-2 consisted of (1?¢????6)-linked mannopyranosyl, (1?¢????6)-linked glucopyranosyl, branched-chain consisted of (1?¢????3,6)-linked galactopyranosyl and terminal consisted of t- l -Rhapyranosyl. The in vitro anti-inflammatory activity was representated through assay of proliferation rate, pro-inflammatory factor (NO) and expressions of proteins on RAW 264.7, the macrophage cell line. The results revealed that EPCP1-2 exhibited significant anti-inflammatory activity by regulating the expression of toll-like receptor 4, mitogen-activated protein kinases, and Nuclear Factor-???oB protein.
机译:来自Crypthecodinium cohnii(EPCP1-2)的胞外多糖是一种海洋胞外多糖,具有多种生物活性。我们从Crypthecodinium cohnii(CP)的发酵液中分离了中性多糖。在这项研究中,分析了一种来自Crypthecodinium cohnii的多糖,并评估了它对巨噬细胞中toll样受体4的蛋白表达和核因子oB途径的抗炎作用。 EPCP1-2的结构特征通过GC(气相色谱)和GC-MS(气相色谱-质谱仪)分析来表征。分子量约为82.5kDa。 EPCP1-2的主链由(1′→6′)连接的甘露吡喃糖基,(1′′→6′)-连接的吡喃吡喃糖基,支链由(1′′→6′′)组成。 3,6)-连接的吡喃半乳糖基和末端由t-1-Rhapyranosyl组成。体外抗炎活性通过测定巨噬细胞系RAW 264.7上的增殖速率,促炎因子(NO)和蛋白质表达来表示。结果表明,EPCP1-2通过调节toll样受体4,有丝分裂原活化的蛋白激酶和核因子-βoB蛋白的表达而表现出显着的抗炎活性。

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