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Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages

BACKGROUND: Sparassis latifolia (S. latifolia) is a precious edible fungus with multiple biological activities. To date, no study has been investigated the underlying molecular mechanism of immunoregulation caused by the neutral polysaccharide of S. latifolia. MATERIALS AND METHODS: To investigate i...

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Autores principales: Qiao, Zening, Zhao, Yue, Wang, Menghao, Cao, Jinling, Chang, Mingchang, Yun, Shaojun, Cheng, Yanfen, Cheng, Feier, Feng, Cuiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515474/
https://www.ncbi.nlm.nih.gov/pubmed/36185691
http://dx.doi.org/10.3389/fnut.2022.994971
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author Qiao, Zening
Zhao, Yue
Wang, Menghao
Cao, Jinling
Chang, Mingchang
Yun, Shaojun
Cheng, Yanfen
Cheng, Feier
Feng, Cuiping
author_facet Qiao, Zening
Zhao, Yue
Wang, Menghao
Cao, Jinling
Chang, Mingchang
Yun, Shaojun
Cheng, Yanfen
Cheng, Feier
Feng, Cuiping
author_sort Qiao, Zening
collection PubMed
description BACKGROUND: Sparassis latifolia (S. latifolia) is a precious edible fungus with multiple biological activities. To date, no study has been investigated the underlying molecular mechanism of immunoregulation caused by the neutral polysaccharide of S. latifolia. MATERIALS AND METHODS: To investigate immunomodulatory mechanism of S. latifolia neutral polysaccharide (SLNP), SLNP was obtained from S. latifolia and its structure, immune receptors and regulation mechanism were studied. RESULTS: S. latifolia neutral polysaccharide consisted of arabinose, galactose, glucose, xylose, and mannose with a molar ratio of 6:12:63:10:5. SLNP was a pyran polysaccharide with a relative molecular weight of 3.2 × 10(5) Da. SLNP promoted the proliferation of RAW264.7, which further induced the secretions of nitric oxide, TNF-α, IL-6, and IFN-β, and upregulated the immune receptor TLR4 expression. Moreover, SLNP increased remarkably the levels of TRAF6, IRF3, JNK, ERK, p38, and p38 mRNA and protein mediated by TLR4. CONCLUSION: S. latifolia neutral polysaccharide regulated the immune function of RAW264.7 through MyD88-dependent and -independent signaling pathways mediated by TLR4 receptor, which suggests that SLNP is a new immunomodulator.
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spelling pubmed-95154742022-09-29 Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages Qiao, Zening Zhao, Yue Wang, Menghao Cao, Jinling Chang, Mingchang Yun, Shaojun Cheng, Yanfen Cheng, Feier Feng, Cuiping Front Nutr Nutrition BACKGROUND: Sparassis latifolia (S. latifolia) is a precious edible fungus with multiple biological activities. To date, no study has been investigated the underlying molecular mechanism of immunoregulation caused by the neutral polysaccharide of S. latifolia. MATERIALS AND METHODS: To investigate immunomodulatory mechanism of S. latifolia neutral polysaccharide (SLNP), SLNP was obtained from S. latifolia and its structure, immune receptors and regulation mechanism were studied. RESULTS: S. latifolia neutral polysaccharide consisted of arabinose, galactose, glucose, xylose, and mannose with a molar ratio of 6:12:63:10:5. SLNP was a pyran polysaccharide with a relative molecular weight of 3.2 × 10(5) Da. SLNP promoted the proliferation of RAW264.7, which further induced the secretions of nitric oxide, TNF-α, IL-6, and IFN-β, and upregulated the immune receptor TLR4 expression. Moreover, SLNP increased remarkably the levels of TRAF6, IRF3, JNK, ERK, p38, and p38 mRNA and protein mediated by TLR4. CONCLUSION: S. latifolia neutral polysaccharide regulated the immune function of RAW264.7 through MyD88-dependent and -independent signaling pathways mediated by TLR4 receptor, which suggests that SLNP is a new immunomodulator. Frontiers Media S.A. 2022-09-14 /pmc/articles/PMC9515474/ /pubmed/36185691 http://dx.doi.org/10.3389/fnut.2022.994971 Text en Copyright © 2022 Qiao, Zhao, Wang, Cao, Chang, Yun, Cheng, Cheng and Feng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Qiao, Zening
Zhao, Yue
Wang, Menghao
Cao, Jinling
Chang, Mingchang
Yun, Shaojun
Cheng, Yanfen
Cheng, Feier
Feng, Cuiping
Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages
title Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages
title_full Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages
title_fullStr Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages
title_full_unstemmed Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages
title_short Effects of Sparassis latifolia neutral polysaccharide on immune activity via TLR4-mediated MyD88-dependent and independent signaling pathways in RAW264.7 macrophages
title_sort effects of sparassis latifolia neutral polysaccharide on immune activity via tlr4-mediated myd88-dependent and independent signaling pathways in raw264.7 macrophages
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515474/
https://www.ncbi.nlm.nih.gov/pubmed/36185691
http://dx.doi.org/10.3389/fnut.2022.994971
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