Suppr超能文献

龙眼活性多糖的结构表征及免疫活性评价。

Structural characterization of an active polysaccharide of longan and evaluation of immunological activity.

机构信息

Engineering Research Center of Utilization of Tropical Polysaccharide Resources, Ministry of Education, College of Food Science and Technology, Hainan University, Haikou 570228, China.

College of Food Science, South China Agricultural University, Guangzhou 510642, China.

出版信息

Carbohydr Polym. 2019 Jun 1;213:247-256. doi: 10.1016/j.carbpol.2019.03.007. Epub 2019 Mar 4.

Abstract

An active polysaccharide (LPD2) was isolated from longan pulp by comparing the effects of polysaccharides on the phagocytosis of macrophages. LPD2 was composed of arabinose, mannose, glucose, and galactose in a molar ratio of 0.25:0.49:1:0.5 with average molecular weight of 9.64 × 10 Da. The main linkages of the sugar residues of LPD2 were (1→4)-β-Glc and (1→6)-β-Man. LPD2 significantly enhanced the lymphocytes proliferation, phagocytosis and NO and IL-6 secretion by macrophage. The anti-TLR2 and anti-TLR4 mAbs markedly suppressed LPD2-mediated NO and IL-6 production. Furthermore, anti-TLR4 or anti-TLR2 plus anti-TLR4 treatment significantly decreased LPD2-induced increase of MyD88, IRAK4, TRAF6 and INOS mRNA expression. Moreover, western blotting analysis showed that LPD2 enhanced the expression of target proteins in MyD88/IRAK4-TRAF6- INOS pathways. These results suggested that LPD2 induced macrophage activation partly via the TLR2- and TLR4-mediated MyD88/IRAK4-TRAF6 signaling pathways. Knowing the structural features and activities of active polysaccharide of longan gives the insights into longan polysaccharide application as an immunomodulatory agent.

摘要

一种活性多糖(LPD2)通过比较多糖对巨噬细胞吞噬作用的影响,从龙眼果肉中分离得到。LPD2 由阿拉伯糖、甘露糖、葡萄糖和半乳糖组成,摩尔比为 0.25:0.49:1:0.5,平均分子量为 9.64×10 Da。LPD2 的糖残基的主要键合方式为(1→4)-β-Glc 和(1→6)-β-Man。LPD2 显著增强了淋巴细胞的增殖、吞噬作用以及巨噬细胞的 NO 和 IL-6 分泌。抗 TLR2 和抗 TLR4 mAb 显著抑制了 LPD2 介导的 NO 和 IL-6 的产生。此外,抗 TLR4 或抗 TLR2 加抗 TLR4 处理显著降低了 LPD2 诱导的 MyD88、IRAK4、TRAF6 和 INOS mRNA 表达的增加。此外,Western blot 分析表明,LPD2 增强了 MyD88/IRAK4-TRAF6-INOS 途径中靶蛋白的表达。这些结果表明,LPD2 通过 TLR2 和 TLR4 介导的 MyD88/IRAK4-TRAF6 信号通路部分诱导了巨噬细胞的激活。了解龙眼活性多糖的结构特征和活性,为龙眼多糖作为免疫调节剂的应用提供了深入了解。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验