Abstract

Lentinan (LNT), a β-glucan from the fruiting bodies of Lentinus edodes, is well known to have immunomodulatory activity. NO and TNF-α are associated with many inflammatory diseases. In this study, we investigated the effects of LNT extracted by sonication (LNT-S) on the NO and TNF-α production in LPS-stimulated murine RAW 264.7 macrophages. The results suggested that treatment with LNT-S not only resulted in the striking inhibition of TNF-α and NO production in LPS-activated macrophage RAW 264.7 cells, but also the protein expression of inducible NOS (iNOS) and the gene expression of iNOS mRNA and TNF-α mRNA. It is surprising that LNT-S enhanced LPS-induced NF-κB p65 nuclear translocation and NF-κB luciferase activity, but severely inhibited the phosphorylation of JNK1/2 and ERK1/2. The neutralizing antibodies of anti-Dectin-1 and anti-TLR2 hardly affected the inhibition of NO production. All of these results suggested that the suppression of LPS-induced NO and TNF-α production was at least partially attributable to the inhibition of JNK1/2 and ERK1/2 activation. This work discovered a promising molecule to control the diseases associated with overproduction of NO and TNF-α.

Highlights

  • High level of Nitric oxide (NO) and TNF-␣ can induce diverse effects on host survival

  • LNT extracted by sonication (LNT-S) Suppresses NO and TNF-␣ Production in LPS-Stimulated RAW 264.7—As described in the Introduction, NO and TNF-␣ are two important inflammatory mediators produced from macrophages corresponding to inflammation

  • LNT-S itself was not effective in inducing notable inducible NOS (iNOS) production. This result indicates that the inhibitory activity of LNT-S toward NO production is through the inhibition of iNOS enzyme expression

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Summary

Background

High level of NO and TNF-␣ can induce diverse effects on host survival. Results: Lentinan inhibits NO and TNF-␣ secretion and phosphorylation of MAP kinases JNK1/2 and ERK1/2. The neutralizing antibodies of anti-Dectin-1 and anti-TLR2 hardly affected the inhibition of NO production All of these results suggested that the suppression of LPS-induced NO and TNF-␣ production was at least partially attributable to the inhibition of JNK1/2 and ERK1/2 activation. Nitric oxide (NO) and tumor necrosis factor-␣ (TNF-␣) are two key molecules in the immunopharmacology which have beneficial biological effects on a variety of normal cells mostly related to immunomodulatory or inflammatory or physiological processes [1,2,3,4] Both of them are two important cytotoxic mediators contributing to the antimicrobial and tumoricidal activity of the macrophages [5,6,7] and exert a key role in. In this study, we investigated the effects of LNT on LPS-induced NO and TNF-␣ secretion from murine macrophage RAW 264.7 cells and on the signal transduction induced by LPS

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