Journal Article

Hydrolyzed Konjac Glucomannan Suppresses IgE Production in Mice B Cells

Uchida, Kazue, Suzuki, Hidenori, Onishi, Nobukazu, Ono, Kazuhisa, Oomizu, Souichi, Hide, Michihiro, Kameyoshi, Yoshikazu, Mihara, Shoji, Yanase, Yuhki

2010

Overview

Background: Oral administration of pulverized Konjac glucomannan (KGM) reduces increased plasma IgE and the amount of Ε-germline transcript (ΕGT) in the spleen, as well as preventing the development of dermatitis in mice. To elucidate the mechanism of action of pulverized KGM, we solubilized KGM and studied its effect on IgE in vitro and in vivo. Methods: Solubilized KGM was prepared by acid hydrolysis, and we analyzed the effective molecular size for the suppression of IgE production and ΕGT in vitro and the level of plasma IgE induced by immunization with ovalbumin in BALB/c mice. Results: The production of IgE and ΕGT in splenic cells, but not purified B cells, was inhibited by hydrolyzed KGM (KGM hydrolyzed with 0.25 N HCl; H-KGM) at the optimal size of between 10 and 500 kDa. However, no effect was observed when H-KGM was substituted with unhydrolyzed KGM in vitro. IgE production from purified B cells cocultured with purified monocytes, but not with purified T cells, was inhibited by H-KGM. The release of IFNγ in cultures of monocytes but in purified B cells with or without T cells was enhanced in the presence of H-KGM. Injection of mice with H-KGM also suppressed the production of plasma IgE and IgG1 but not IgG2a in vivo. Conclusion: KGM at an optimal size prevents germline class-switching and IgE production both in vitro and in vivo. H-KGM may be useful as a tool to study the mechanism of action of KGM and as a dietary supplement to prevent atopic diseases.

• Publisher: Karger,S. Karger AG
• Subject: Animals / B-Lymphocytes - cytology / B-Lymphocytes - drug effects / B-Lymphocytes - metabolism / Biological and medical sciences / Coculture Techniques / Cytokines - metabolism / Dermatitis / Dietary supplements / Fundamental and applied biological sciences. Psychology / Fundamental immunology / Gene Expression - drug effects / Gene Expression - genetics / Hydrolysis / Immunoglobulin Class Switching - drug effects / Immunoglobulin E - biosynthesis / Immunoglobulin E - blood / Immunoglobulin E - immunology / Immunoglobulin epsilon-Chains - genetics / Immunoglobulin G - blood / Immunoglobulin G - immunology / Immunoglobulins / Immunopathology / Interferon-gamma - metabolism / Lymphocytes - drug effects / Lymphocytes - metabolism / Male / Mannans - chemistry / Mannans - pharmacology / Medical sciences / Mice / Mice, Inbred BALB C / Monocytes - cytology / Monocytes - drug effects / Monocytes - metabolism / Original Paper / Ovalbumin - immunology / Rodents / Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis / Spleen - cytology / T-Lymphocytes - cytology