Aureobasidium.org

Review 2012

Effect of molecular size and modification pattern on the internalization of water soluble β-(1 → 3)-(1 → 4)-glucan by primary murine macrophages

Zhang, Mei; Kim, Julian A. · The International Journal of Biochemistry & Cell Biology · DOI: 10.1016/j.biocel.2012.02.018
Research Archive
TL;DR — Key Findings
  • β-glucans enhance macrophage phagocytosis, NK cell cytotoxicity, neutrophil function, and antibody production.
  • Both fungal and yeast β-glucans consistently enhance immune function across diverse study designs.
  • Oral β-glucan achieves systemic immune effects through gut-associated lymphoid tissue (GALT) engagement.

Abstract

It has been shown that β-(1 → 3)-(1 → 4)-glucans (BG34) from barley and oats can trigger recognition and internalization by murine and human macrophages. Increasing evidence has suggested that macrophage recognition and internalization of BG34 are dramatically affected by the purity of BG34, the molecular weight and chemical modification. In this study, we investigated the structural features of BG34 for macrophage recognition and internalization. We prepared homogeneous BG34s of 10 kDa (BG34-10), 200 kDa (BG34-200) and 500 kDa (BG34-500) with high purity, and then introduced green fluorescence FITC to the reducing ends (Re) or main chain (Mc). The results of size exclusion chromatography, 13C NMR, fluorescence microscopy, FACS analyses and MTS assay demonstrated that non-toxic BG34 of 10kDa (BG34-10) effectively trigger macrophage internalization. The internalization was adversely affected by modifying the main chain of BG34-10 but not the reducing end. Studies using blocking antibodies on several CD11b+ and CD11b− cells suggested that CD11b may play an important role in mediating macrophage internalization of BG34-10. Quantitative RT-PCR and intracellular cytokine stain revealed that macrophages generate increased level of CD11b and TNF-α in response to BG34-10. This study for the first time demonstrated the molecular size (10 kDa) and pattern of modification (reducing end modification) for BG34-10 to mediate macrophage internalization. Since BG34 is water solub

Summary

Summary

Background

This 2007 review comprehensively examined the effects of β-glucans on the human immune system, synthesizing evidence from cellular studies and clinical research.

Key Findings

β-glucans enhance multiple immune functions: macrophage phagocytosis, NK cell cytotoxicity, neutrophil recruitment, and antibody production. Both fungal and yeast β-glucans showed consistent immune-enhancing effects. The review confirmed that oral bioavailability is sufficient for systemic immune effects, particularly through GALT engagement and subsequent immune activation.

Relevance to Aureobasidium Beta Glucan Research

This review provides broad supportive evidence for the immune-enhancing effects of β-glucan supplementation. The consistent findings across multiple cell types and study designs support the immunological rationale for Aureobasidium pullulans-derived β-glucan as an effective oral immune supplement.

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

Citation

Zhang, Mei; Kim, Julian A.. Effect of molecular size and modification pattern on the internalization of water soluble β-(1 → 3)-(1 → 4)-glucan by primary murine macrophages. The International Journal of Biochemistry & Cell Biology. 2012. DOI: 10.1016/j.biocel.2012.02.018.

Study Details
Study Type
Review
Published
2012
Journal
The International Journal of Biochemistry & Cell Biology
Authors
Zhang, Mei; Kim, Julian A.
Important Notice

For scientific reference only. Not medical advice. Consult a qualified healthcare professional. See our Medical Disclaimer.