Abstract

BackgroundThe present study extensively aimed to evaluate the underlying mechanism of the immunomodulatory and anti-inflammatory effects of Phellinus linteus mycelium (PLM).MethodsTo assess whether PLM influences the production of markers related to inflammation, Lipopolysaccharide (LPS)-stimulated RAW264.7 cells were treated with PLM (50, 100, 200, and 500 μg/mL). Splenocyte, thymus, peritoneal exudate cells (PEC), and peripheral blood mononuclear cells (PBMC) were isolated from the Balb/c mice treated with Korean red ginseng or PLM once a day for 5 weeks. Moreover, all mice except normal mice were stimulated with 10% proteose peptone (PP) treated 3 days before the sacrifice and 2% starch treated 2 days before the sacrifice. Subsequently, the cytotropic substance was evaluated by using flow cytometry analysis and ELISA assay.ResultsPLM200 treatment significantly suppressed the production of nitric oxide (NO) and prostaglandin E2 (PGE2) and inhibited the release of proinflammatory cytokines such as interleukin (IL)-6, IL-1β, and tumor necrosis factor (TNF)-α dose-dependently in the LPS-stimulated RAW264.7 cells. PLM200 supplementation showed a significant increase in IL-2, IL-12, and interferon (IFN)-γ production and upregulated the ratio of IFN-γ (T-helper type 1, Th1) to IL-4 (T-helper type 2, Th2) in splenocytes. After PLM200 treatment, the significant elevation of CD4+CD25+, CD4+&CD8+, and CD4+CD69+ treatment were detected in thymus. Moreover, CD4+ and CD4+CD69+ in PBMC and CD69+ in PEC were also shown in a significant increase.ConclusionsTaken together, these results showed an immunomodulatory effect of PLM about an elevated INF-γ/IL4 ratio, as an index of Th1/Th2, as well as the anti-inflammatory effect in the LPS-stimulated RAW264.7 cells. Therefore, our findings demonstrate that PLM possesses immunostimulatory and anti-inflammatory effects.

Highlights

  • The present study extensively aimed to evaluate the underlying mechanism of the immunomodula‐ tory and anti-inflammatory effects of Phellinus linteus mycelium (PLM)

  • Effects of PLM on cytotoxicity, nitric oxide (NO), ­prostaglandin E2 (PGE2), tumor necrosis factor (TNF)‐α, IL‐6, and IL‐1β productions in RAW264.7 cells To assess whether PLM influences the production of markers related to inflammation, LPS-stimulated RAW264.7 cells were treated with PLM

  • We investigated the inhibitory effect of PLM on PGE2, IL-6, IL-1β, and TNF-α generation in LPS-treated RAW264.7 cells

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Summary

Introduction

The present study extensively aimed to evaluate the underlying mechanism of the immunomodula‐ tory and anti-inflammatory effects of Phellinus linteus mycelium (PLM). When pathogens reach the initial barriers of the skin or a mucosal surface, Shin et al BMC Complement Med Ther (2021) 21:269 including tissue macrophages and dendritic cells. This program causes by the generation of an antipathogen state and the production of numerous inflammatory cytokines and chemokines [5]. M1-like macrophages produce proinflammatory cytokines such as TNF-α, type I interferon (IFN), IL-1β, IL-6, IL-12, and several chemokines and induce Th1 response activation under acute inflammatory responses. M2-like macrophages produce anti-inflammatory cytokines, such as IL-4, IL-13, IL-10, and induce Th2 response activation [11]. If the immune response fails to effectively control the pathogen, it leads to clinical disease

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