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An arabinogalactan isolated from Boswellia carterii: Purification, structural elucidation and macrophage stimulation via NF-κB and MAPK pathways

[Display omitted] •Water soluble acidic polysaccharides were isolated and purified from Boswellia carterii.•The molecular weights of polysaccharides ranged from 295.5 to 504.7 × 103 g/mol.•Polysaccharides exhibited notable RAW264.7 macrophage stimulating activity.•Macrophages were activated through...

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Bibliographic Details
Published in:Journal of functional foods 2019-01, Vol.52, p.450-458
Main Authors: Bahramzadeh, Saman, Tabarsa, Mehdi, You, SangGuan, Yelithao, Khamphone, Klochkov, Vladimir, Ilfat, Rakhmatullin
Format: Article
Language:English
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Summary:[Display omitted] •Water soluble acidic polysaccharides were isolated and purified from Boswellia carterii.•The molecular weights of polysaccharides ranged from 295.5 to 504.7 × 103 g/mol.•Polysaccharides exhibited notable RAW264.7 macrophage stimulating activity.•Macrophages were activated through NF-κB and MAPK pathways via TLR4 and TLR2. Polysaccharides from Boswellia carterii were isolated using hot water and fractionated on a DEAE Sepharose Fast Flow column to evaluate their structural characteristics and macrophage stimulating capacities. Crude and fractionated polysaccharides (BCF1 and BCF2) were mainly consisted of different amounts of neutral sugars (63.7–83.3%) and uronic acids (6.2–22.3%). The weight average molecular weights (Mw) of polysaccharides greatly varied between 295.5 and 504.7 × 103 g/mol. The BCF2 was a highly active polysaccharide on RAW264.7 murine macrophage cells inducing considerable release of nitric oxide and proinflammatory cytokines including TNF-α, IL-1β and IL-6. The presence of p-NF-κB, p-JNK, p-ERK and p-p38 proteins in the cytoplasm of the stimulated macrophages indicated the activation of cells via NF-κB and MAPKs signaling pathways which was followed after CBF2-macrophage interaction through TLR4 and TLR2 receptors. The most potent macrophage activating polysaccharide, BCF2, contained a backbone of (1 → 6)-β-galactopyranosyl units branched at C-3.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2018.11.025