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Purification, Structural Characterization and Immunomodulatory Effects of Polysaccharides from Amomumvillosum Lour. on RAW 264.7 Macrophages

机译:氨形状乳清醇的多糖的纯化,结构表征和免疫调节作用。在原始264.7巨噬细胞上

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摘要

Amomum Villosum Lour. (A. villosum) is a folk medicine that has been used for more than 1300 years. However, study of the polysaccharides of A. villosum is seriously neglected. The objectives of this study are to explore the structural characteristics of polysaccharides from A. villosum (AVPs) and their effects on immune cells. In this study, the acidic polysaccharides (AVPG-1 and AVPG-2) were isolated from AVPs and purified via anion exchange and gel filtration chromatography. The structural characteristics of the polysaccharides were characterized by methylation, HPSEC-MALLS-RID, HPLC, FT-IR, SEM, GC-MS and NMR techniques. AVPG-1 with a molecular weight of 514 kDa had the backbone of → 4)-α-d-Glcp-(1 → 3,4)-β-d-Glcp-(1 → 4)-α-d-Glcp-(1 →. AVPG-2 with a higher molecular weight (14800 kDa) comprised a backbone of → 4)-α-d-Glcp-(1 → 3,6)-β-d-Galp-(1 → 4)-α-d-Glcp-(1 →. RAW 264.7 cells were used to investigate the potential effect of AVPG-1 and AVPG-2 on macrophages, and lipopolysaccharide (LPS) was used as a positive control. The results from bioassays showed that AVPG-2 exhibited stronger immunomodulatory activity than AVPG-1. AVPG-2 significantly induced nitric oxide (NO) production as well as the release of interleukin (IL)-6 and tumor necrosis factor alpha (TNF-α), and upregulated phagocytic capacities of RAW 264.7 cells. Real-time PCR analysis revealed that AVPG-2 was able to turn the polarization of macrophages to the M1 direction. These results suggested that AVPs could be explored as potential immunomodulatory agents of the functional foods or complementary medicine.
机译:Amomum villosum lour。 (A. Villosum)是一款已被使用超过1300年的民间医学。然而,对villosum的多糖的研究严重被忽视了。本研究的目的是探讨来自A. Villosum(AVPS)的多糖的结构特征及其对免疫细胞的影响。在该研究中,从AVPS中分离酸性多糖(AVPG-1和AVPG-2)并通过阴离子交换和凝胶过滤色谱纯化。通过甲基化,HPSec-Mall-RiD,HPLC,FT-IR,SEM,GC-MS和NMR技术表征多糖的结构特征。分子量为514 kda的AVPG-1具有→4)-α-D-GLCP-(1→3,4)-β-D-GLCP-(1→4)-α-D-GLCP-的骨干(1→。具有较高分子量(14800kDa)的AVPG-2包括→4)-α-D-GLCP-(1→3,6)-β-D-Galp-(1→4)的骨干 - α-D-GLCP-(1→。原始264.7细胞用于研究AVPG-1和AVPG-2对巨噬细胞的潜在效果,而脂多糖(LPS)用作阳性对照。生物测定的结果表明AVPG -2表现出比AVPG-1更强的免疫调节活性。AVPG-2显着诱导一氧化氮(NO)生产以及白细胞介素(IL)-6和肿瘤坏死因子α(TNF-α)的释放,以及上调的吞噬能力RAW 264.7细胞。实时PCR分析显示,AVPG-2能够将巨噬细胞的极化转向M1方向。这些结果表明AVPS可以探索为功能性食品或互补药物的潜在免疫调节剂。

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