A novel homogeneous polysaccharide (LYP-S3) that promotes
the M2
polarization of macrophages was obtained from large yellow tea by
a bioactivity-guided sequential isolation procedure and activity evaluation
in the present study. Structural characterization revealed that LYP-S3
has an average molecular weight of 28.6 kDa and is composed of rhamnose,
arabinose, galactose, glucose, and galacturonic acid at the molar
ratio of 8.08:11.66:11.77:3.96:58.02. The main backbone of LYP-S3
consists of →4)-α-d-GalpA-6-OMe-(1→,
β-d-GalpA-(1→, →4)-β-d-Galp-(→1, and →β-d-Galp-(1→, and the branches are composed
of α-l-Araf-(→1, →5)-α-l-Araf-(1→, →2,4)-β-l-Rhap-(1→, →2)-β-l-Rhap-(1→, and →4)-β-d-Glcp-(1→. An in vitro bioactivity evaluation
assay showed that LYP-S3 remarkably reduced the expression of M1 macrophage
markers and increased the expression of M2 macrophage markers. In
addition, LYP-S3 inhibited adipocyte differentiation and adipogenesis
in 3T3-L1 adipocytes and blocked macrophage migration toward 3T3-L1
adipocytes in the cocultures of bone-marrow-derived monocytes and
3T3-L1 adipocytes. Furthermore, LYP-S3 promoted the M2 polarization
of macrophages in cocultures. These findings suggested that LYP-S3
has a potential function in preventing inflammation and obesity.