2020
DOI: 10.1016/j.carbpol.2020.116469
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A heteropolysaccharide purified from leaves of Ilex latifolia displaying immunomodulatory activity in vitro and in vivo

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Cited by 28 publications
(13 citation statements)
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“…In the aggregated state, an irregular branch network structure with an uneven surface was noted, suggesting an amorphous structure of GFPA. The surface of GFPA was uneven in thickness and showed crests and sags, which may have been caused by the branched structure of GFPA ( Figures 2G–J ) ( 31 ).…”
Section: Resultsmentioning
confidence: 99%
“…In the aggregated state, an irregular branch network structure with an uneven surface was noted, suggesting an amorphous structure of GFPA. The surface of GFPA was uneven in thickness and showed crests and sags, which may have been caused by the branched structure of GFPA ( Figures 2G–J ) ( 31 ).…”
Section: Resultsmentioning
confidence: 99%
“…Shi et al . (2020) suggested that Ilex latifolia Thunb polysaccharide (ILP50‐2) could significantly promote the secretion of NO and ROS in zebrafish, which exhibited immunoregulatory effects in vivo . In the present study, we only evaluated the in vitro immunomodulatory activity of PGPIV‐1‐a on macrophages.…”
Section: Resultsmentioning
confidence: 99%
“…Effects of PGPIV-1-a on NO, TNF-a and IL-6 production of RAW 264.7 cells Figure 5 Triple-helical conformation analysis of PGPIV-1-a. When macrophages are activated, they can induce the production of NO and cytokine (TNF-a and IL-6), which plays indispensable roles in immunomodulatory responses (Sun et al, 2015). Nitric oxide (NO) is an intracellular messenger, which contributes to defend the host against the invasion of pathogens and mediates a variety of biological functions (Du et al, 2016).…”
Section: Immunomodulatory Activity Of Pgpiv -1-amentioning
confidence: 99%
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“…The phagocytic ability of RAW264.7 macrophages after treating with EGCG was determined by the neutral red assay, according to the previous method. , Briefly, the cells seeded in 96-well plates (1 × 10 5 cells/mL) were stimulated into the M1 phenotype and treated with different concentrations of EGCG (1, 5, 10, 25 μM) for 24 h simultaneously. The control group was set up as the cells without treating with EGCG.…”
Section: Methodsmentioning
confidence: 99%