Abstract

Agaricus blazei Murill is an edible and medicinal mushroom. In the previous study, we have proved that extracts of A. blazei inhibit human peripheral blood mononuclear cell (PBMC) proliferation activated with phytohemagglutinin (PHA). Currently, we purified 4-hydroxy-17-methylincisterol (4-HM; C21H33O3) from A. blazei investigated its regulatory effects on cytokine productions and cell proliferation of PBMC induced by PHA. The results indicated that 4-HM suppressed, in activated PBMC, the production and mRNA expression of interleukin-2 (IL-2), IL-4, tumor necrosis factor-α, and interferon-γ in a concentration-dependent manner. This inhibition was not related to cell viability. While 4-HM did not affect ERK phosphorylation and its downstream c-fos gene expression in PBMC induced by PHA, it decreased both NF-AT and NF-κB activation. The upstream signaling of NF-AT and NF-κB, intracellular calcium concentrations ([Ca2+]i), and protein kinase C theta (PKC θ) activation in PHA-treated PBMC were reduced by 4-HM. The data demonstrated that the suppressant effects of 4-HM on cell proliferation in PBMC activated by PHA appeared to be mediated, at least in part, through inhibition of Ca2+ mobilization and PKC θ activation, NF-AT and NF-κB activation, and cytokine transcripts and productions of PBMC. We suggested that A. blazei contained a potential immunomodulator 4-HM.

Highlights

  • Agaricus blazei Murill belongs to Basidiomycete and is used as an alternative medicine in Brazil for a long time [1]

  • We have proved that ethanolic extracts from A. blazei inhibit cytokine productions and cell proliferation in human peripheral blood mononuclear cells (PBMC) induced by phytohemagglutinin (PHA) [8]

  • At 10 μM, the stimulated productions of IL-2, IL-4, IFN-γ, and tumor necrosis factor-α (TNF-α) in activated PBMC were completely blocked by 4HM, with their concentrations returning to almost the same as those produced in resting cells

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Summary

Introduction

Agaricus blazei Murill belongs to Basidiomycete and is used as an alternative medicine in Brazil for a long time [1]. The most anticipated pharmacological effect of A. blazei is that a proteoglucan (FIII-2-b) isolated from it has antitumor activity through modulation of the natural killer cell activity and macrophage activation [4, 5]. Linoleic acid isolated form A. blazei is a bactericidal agent [6]. Steroids identified from A. blazei are cytotoxic against HeLa cells [7]. We have proved that ethanolic extracts from A. blazei inhibit cytokine productions and cell proliferation in human peripheral blood mononuclear cells (PBMC) induced by phytohemagglutinin (PHA) [8]. PHA is a mitogen for T lymphocytes. It binds to N-acetylgalactosamine glycoproteins expressed on the surface of T cells activates the cells to produce cytokines and proliferate [9].

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