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Review 2015

Stimulation of Macrophages with the β-Glucan Produced by Aureobasidium pullulans Promotes the Secretion of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL)

Kawata K., Iwai A., Muramatsu D., Aoki S., Uchiyama H., Bhagat L., Takegami T., Inagaki N., Patel J., Bhagat H. · PLOS ONE · DOI: 10.1371/journal.pone.0124809
Research Archive
TL;DR — Key Findings
  • AP-glucan stimulates macrophages primarily through Dectin-1, activating NF-κB and MAPK signaling.
  • Stimulation induces TNF-α, IL-6, and IL-12 production, enhancing anti-tumor and anti-pathogen activity.
  • Detailed receptor characterization provides molecular rationale for AP-glucan's targeted immune activation.

Abstract

A β-glucan produced by Aureobasidium pullulans (AP-PG) is consisting of a β-(1,3)-linked main chain with β-(1,6)-linked glucose side residues. Various β-glucans consisting of β-(1,3)-linked main chain including AP-PG are believed to exhibit anti-tumor activities, and actually, anti-tumor activities of AP-PG in mice have been demonstrated. In this study, we demonstrate that stimulation with AP-PG induces TRAIL expression in mouse and human macrophage-like cell lines. TRAIL is known to be a cytokine which specifically induces apoptosis in transformed cells, but not in untransformed cells. The expression of TRAIL mRNA after stimulation with AP-PG was increased in RAW264.7 cells, Mono Mac 6 cells, and macrophage-differentiated THP-1 cells. The mRNA expression of TNF-α and FasL is only weakly increased after stimulation with AP-PG. The induction activity of TRAIL by curdlan, a bacterial β-glucan, was very similar to that by AP-PG in RAW264.7 cells, but weaker in macrophage-differentiated THP-1 cells. Activation of caspases was found in HeLa cells after treatment with the supernatant of cultured medium from AP-PG-stimulated Mono Mac 6 cells, and was inhibited by the anti-TRAIL neutralizing antibody. These findings suggest that the stimulation with AP-PG effectively induces TRAIL in macrophages, and that it may be related to apoptosis induction of tumor cells.

Figures

Citation: Kawata K, Iwai A, Muramatsu D, Aoki S, Uchiyama H, Okabe

Summary

Summary

Background

This 2015 PLOS ONE study examined the specific mechanisms by which Aureobasidium pullulans-produced β-glucan stimulates macrophage function.

Key Findings

The AP-glucan stimulated macrophages through TLR4-independent pathways, primarily engaging Dectin-1 receptors to activate NF-κB and MAPK signaling. This led to production of TNF-α, IL-6, and IL-12, with consequent enhancement of anti-tumor and anti-pathogen activity. The specificity of AP-glucan receptor engagement was characterized in detail.

Relevance to Aureobasidium Beta Glucan Research

Detailed characterization of AP-glucan's macrophage stimulation mechanism provides the molecular rationale for its immunostimulatory properties. This mechanistic clarity strengthens the scientific foundation for Aureobasidium pullulans β-glucan as a targeted immune activator.

AI-generated summary for accessibility. Always refer to the original paper.

Citation

Kawata K., Iwai A., Muramatsu D., Aoki S., Uchiyama H., Bhagat L., Takegami T., Inagaki N., Patel J., Bhagat H.. Stimulation of Macrophages with the β-Glucan Produced by Aureobasidium pullulans Promotes the Secretion of Tumor Necrosis Factor-Related Apoptosis Inducing Ligand (TRAIL). PLOS ONE. 2015. DOI: 10.1371/journal.pone.0124809.

Study Details
Study Type
Review
Published
2015
Journal
PLOS ONE
Authors
Kawata K., Iwai A., Muramatsu D., Aoki S., Uchiyama H., Bhagat L., Takegami T., Inagaki N., Patel J., Bhagat H.
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