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Phagocytic Effects of β-Glucans from the Mushroom Coriolus versicolor are Related to Dectin-1, NOS, TNF-α Signaling in Macrophages
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  • Phagocytic Effects of β-Glucans from the Mushroom Coriolus versicolor are Related to Dectin-1, NOS, TNF-α Signaling in Macrophages
  • Phagocytic Effects of β-Glucans from the Mushroom Coriolus versicolor are Related to Dectin-1, NOS, TNF-α Signaling in Macrophages
저자명
Jang. Seon-A,Kang. Se-Chan,Sohn. Eun-Hwa
간행물명
Biomolecules & therapeutics
권/호정보
2011년|19권 4호|pp.438-444 (7 pages)
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한국응용약물학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

The mushroom Coriolus versicolor contains biologically active polysaccharides, most of which belong to the ${eta}$-glucan group. Diverse physicochemical properties, due to different sources and isolated types of ${eta}$-glucans, can induce distinct biological activities. We investigated the effects of ${eta}$-glucans from C. versicolor on phagocytic activity, nitric oxide (NO), TNF-${alpha}$ production, and signaling of dectin-1, a well-known ${eta}$-glucan receptor, in macrophages. ${eta}$-Glucans increased phagocytic activity and TNF-${alpha}$ and NO-iNOS/eNOS production. Laminarin, a specific inhibitor of dectin-1, showed strong inhibitory effects on phagocytosis and subsequent TNF-${alpha}$, iNOS, and eNOS production increased by ${eta}$-glucans, indicating that ${eta}$-glucans reacts with dectin-1 receptors. We examined whether the aforementioned cytokines were involved in the signaling pathway from the dectin-1 receptor to phagocytosis, and found that the inhibition of iNOS, eNOS, and TNF-${alpha}$ receptors significantly decreased ${eta}$-glucan-induced phagocytosis. In conclusion, our study showed that dectin-1 signaling, triggered by ${eta}$-glucans, subsequently elicited TNF-${alpha}$ and NO-iNOS/eNOS production, and that these molecules seem to act as secondary molecules that cause eventual phagocytosis by macrophages. These findings suggest that C. versicolor could be used as a nutritional medicine that may be useful in the treatment of infectious disease.