Isolation, structural elucidation and immuno-stimulatory properties of polysaccharides from Cuminum cyminum
•Water-soluble polysaccharides were purified from Cuminum cyminum.•Polysaccharides activated RAW264.7 cells to produce proinflammatory mediators.•Polysaccharides stimulated NK-92 cells to produce TNF-α, INF-γ and perforin.•RAW264.7 and NK cells were activated through NF-κB and MAPK signaling pathway...
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Published in: | Carbohydrate polymers Vol. 230; p. 115636 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Elsevier Ltd
15-02-2020
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Subjects: | |
Online Access: | Get full text |
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Summary: | •Water-soluble polysaccharides were purified from Cuminum cyminum.•Polysaccharides activated RAW264.7 cells to produce proinflammatory mediators.•Polysaccharides stimulated NK-92 cells to produce TNF-α, INF-γ and perforin.•RAW264.7 and NK cells were activated through NF-κB and MAPK signaling pathways.•The most active polysaccharide contained high (1→4)-Galp and (1→2)-Arap units.
The aim of the present study was to evaluate the effect of water-soluble polysaccharides from Cuminum cyminum to induce inflammatory response in immune cells and understand their underlying mechanisms. Weight average molecular weight (Mw) of polysaccharides varied between 191.4–512.2 × 103 g/mol. Polysaccharides induced RAW264.7 cells to release nitric oxide and express TNF-α, IL-1β, IL-6 and IL-12 inflammatory cytokines. Polysaccharides activated NK-92 cells to produce TNF-α, IFN-γ, perforin, granzyme B, NKG2D and FasL. Activations of RAW264.7 and NK-92 cells were through NF-κB and MAPKs signal pathways indicated by the presence of phosphorylated NF-κB, ERK, JNK and p38 proteins. The polysaccharide structure was mainly constituted of →4)-Galp-(1→, →3)-Galp-(1→, →2)-Arap-(1→ and →2)-Arap-(1→ glycosidic linkages. Overall results suggested that polysaccharides from C. cyminum possessing lower MW and greater expanded conformation more effectively stimulate RAW264.7 and NK-92 cells and thus could be considered for further studies on their biomedical applications. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2019.115636 |