A Polysaccharide Isolated from Codonopsis pilosula with Immunomodulation Effects Both In Vitro and In Vivo

In this study, an acidic polysaccharide from Nannf. var. (Nannf.) L. T. Shen (WCP-I) and its main fragment, WCP-Ia, obtained after pectinase digestion, were structurally elucidated and found to consist of a rhamnogalacturonan I (RG-I) region containing both arabinogalactan type I (AG-I) and type II...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2019-10, Vol.24 (20), p.3632
Hauptverfasser: Zou, Yuan-Feng, Zhang, Yan-Yun, Fu, Yu-Ping, Inngjerdingen, Kari Tvete, Paulsen, Berit Smestad, Feng, Bin, Zhu, Zhong-Kai, Li, Li-Xia, Jia, Ren-Yong, Huang, Chao, Song, Xu, Lv, Cheng, Ye, Gang, Liang, Xiao-Xia, He, Chang-Liang, Yin, Li-Zi, Yin, Zhong-Qiong
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Sprache:eng
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Zusammenfassung:In this study, an acidic polysaccharide from Nannf. var. (Nannf.) L. T. Shen (WCP-I) and its main fragment, WCP-Ia, obtained after pectinase digestion, were structurally elucidated and found to consist of a rhamnogalacturonan I (RG-I) region containing both arabinogalactan type I (AG-I) and type II (AG-II) as sidechains. They both expressed immunomodulating activity against Peyer's patch cells. Endo-1,4-β-galactanase degradation gave a decrease of interleukine 6 (IL-6) production compared with native WCP-I and WCP-Ia, but exo-α-l-arabinofuranosidase digestion showed no changes in activity. This demonstrated that the stimulation activity partly disappeared with removal of β-d-(1→4)-galactan chains, proving that the AG-I side chain plays an important role in immunoregulation activity. WCP-Ia had a better promotion effect than WCP-I in vivo, shown through an increased spleen index, higher concentrations of IL-6, transforming growth factor-β (TGF-β), and tumor necrosis factor-α (TNF-α) in serum, and a slight increment in the secretory immunoglobulin A (sIgA) and CD4 /CD8 T lymphocyte ratio. These results suggest that β-d-(1→4)-galactan-containing chains in WCP-I play an essential role in the expression of immunomodulating activity. Combining all the results in this and previous studies, the intestinal immune system might be the target site of WCP-Ia.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules24203632