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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >A polysaccharide isolated from the fruits of Physalis alkekengi L. induces RAW264.7 macrophages activation via TLR2 and TLR4-mediated MAPK and NF-kappa B signaling pathways
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A polysaccharide isolated from the fruits of Physalis alkekengi L. induces RAW264.7 macrophages activation via TLR2 and TLR4-mediated MAPK and NF-kappa B signaling pathways

机译:从液体alAkekengi L的果实中分离的多糖诱导Raw264.7通过TLR2和TLR4介导的MAPK和NF-Kappa发信号通路的巨噬细胞激活

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摘要

Polysaccharides from Physalis alkekengi L. have been proven to possess many biological activities. In our previous study, a homogeneous polysaccharide (PPSB) was extracted and purified from the fruits of Physalis alkekengi L., and the structure characterization was analyzed. The present study aimed to investigate the effects of PPSB on RAW264.7 macrophage cells activation and the underlying molecular mechanism. PPSB could activate RAW264.7 cells by not only enhancing the pinocytic and phagocytic activity, but also promoting the production of NO, ROS, TNF-alpha, and IL-6 in RAW264.7 cells. Meanwhile, PPSB up-regulated the expression of major histocompatibility complex (MHC-I/II) and costimulatory molecules such as CD40, CD80 and CD86. Mechanism studies showed that PPSB induced the activation of mitogen-activated protein kinases (MAPKs) and nuclear factor-kappa B (NF-kappa B) pathways. Moreover, the production of NO, TNF-alpha and IL-6 induced by PPSB in RAW264.7 cells were suppressed by specific MAPKs and NF-kappa B inhibitors. Further experiments with blocking antibodies demonstrated that the releases of NO, INF-alpha and IL-6 and the activation of MAPKs and NF-kappa B induced by PPSB were decreased after TLR2 and TLR4 were blocked. Our date illustrated that PPSB was capable of activating the RAW264.7 cells via MAPKs and NF-kappa B signaling mediated by TLR2 and TLR4. (C) 2019 Elsevier B.V. All rights reserved.
机译:来自Physalis Alkekengi L的多糖已被证明具有许多生物学活动。在我们以前的研究中,从physalisAlkekengi L的果实中提取并纯化均相多糖(PPSB),分析结构表征。本研究旨在探讨PPSB对Raw264.7巨噬细胞活化和底层分子机制的影响。 PPSB可以通过不仅增强针状细胞和吞噬活性而活化的Raw264.7细胞,而且可以在Raw264.7细胞中促进NO,ROS,TNF-α和IL-6的产生。同时,PPSB上调主要组织相容络合物(MHC-I / II)和共刺激分子如CD40,CD80和CD86的表达。机制研究表明,PPSB诱导丝裂原激活蛋白激酶(MAPK)和核因子-Kappa B(NF-Kappa B)途径的活化。此外,通过特定MAPK和NF-Kappa B抑制剂抑制了PPSB中PPSB诱导的NO,TNF-α和IL-6的产生。通过阻断抗体的进一步实验表明,在TLR2和TLR4被封闭后,通过PPSB诱导的NO,INF-α和IL-6的释放和MAPK和NF-κB的活化降低。我们的日期说明了PPSB能够通过MAPK和NF-Kappa B信令激活RAW264.7细胞,由TLR2和TLR4介导。 (c)2019 Elsevier B.v.保留所有权利。

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