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GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist
Ganoderma sinense is a Chinese unique medicinal fungus that has been used in folk medicine for thousands of years. Polysaccharides are considered to be biologically active ingredients due to their immune-modulating functions. Previously we found that GSP-2, a new polysaccharide isolated from Ganoder...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707555/ https://www.ncbi.nlm.nih.gov/pubmed/31442262 http://dx.doi.org/10.1371/journal.pone.0221636 |
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author | Liu, Kai-Sheng Zhang, Cheng Dong, Hong-Liang Li, Kai-Kai Han, Quan-Bin Wan, Yong Chen, Rui Yang, Fang Li, Hai-Li Ko, Chun-Hay Han, Xiao-Qiang |
author_facet | Liu, Kai-Sheng Zhang, Cheng Dong, Hong-Liang Li, Kai-Kai Han, Quan-Bin Wan, Yong Chen, Rui Yang, Fang Li, Hai-Li Ko, Chun-Hay Han, Xiao-Qiang |
author_sort | Liu, Kai-Sheng |
collection | PubMed |
description | Ganoderma sinense is a Chinese unique medicinal fungus that has been used in folk medicine for thousands of years. Polysaccharides are considered to be biologically active ingredients due to their immune-modulating functions. Previously we found that GSP-2, a new polysaccharide isolated from Ganoderma sinense, exerts an immunomodulatory effect in human peripheral blood mononuclear cells but the underlying mechanism is unclear. The present study aimed to investigate how GSP-2 triggers immunologic responses and the implicated signaling pathways. GSP-2 effects were investigated both in a macrophagic cell line, RAW264.7, and in primary macrophages. Moreover, the molecular basis of GSP-2 recognition by immune cells, and the consequent activation of signaling cascades, were explored by employing recombinant human HEK293-TLR-Blue clones, individually overexpressing various Toll-like receptors. GSP-2 dose-dependently induced the overexpression of Toll-like receptor 4 (TLR4) but did not affect the expression of other TLRs. Moreover, GSP-2 induced TNFα secretion in primary macrophages from wild-type, but not TLR4-knockout mice. In addition, GSP-2 upregulated TLR4 protein expression and activated the MAPK pathway in RAW246.7 macrophages. Finally, GSP-2 induced the production of the cytokines TNFα, IL1β, and IL6. Our data demonstrated that GSP-2 was specifically recognized by TLR4, promoting cytokine secretion and immune modulation in macrophages. |
format | Online Article Text |
id | pubmed-6707555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67075552019-09-04 GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist Liu, Kai-Sheng Zhang, Cheng Dong, Hong-Liang Li, Kai-Kai Han, Quan-Bin Wan, Yong Chen, Rui Yang, Fang Li, Hai-Li Ko, Chun-Hay Han, Xiao-Qiang PLoS One Research Article Ganoderma sinense is a Chinese unique medicinal fungus that has been used in folk medicine for thousands of years. Polysaccharides are considered to be biologically active ingredients due to their immune-modulating functions. Previously we found that GSP-2, a new polysaccharide isolated from Ganoderma sinense, exerts an immunomodulatory effect in human peripheral blood mononuclear cells but the underlying mechanism is unclear. The present study aimed to investigate how GSP-2 triggers immunologic responses and the implicated signaling pathways. GSP-2 effects were investigated both in a macrophagic cell line, RAW264.7, and in primary macrophages. Moreover, the molecular basis of GSP-2 recognition by immune cells, and the consequent activation of signaling cascades, were explored by employing recombinant human HEK293-TLR-Blue clones, individually overexpressing various Toll-like receptors. GSP-2 dose-dependently induced the overexpression of Toll-like receptor 4 (TLR4) but did not affect the expression of other TLRs. Moreover, GSP-2 induced TNFα secretion in primary macrophages from wild-type, but not TLR4-knockout mice. In addition, GSP-2 upregulated TLR4 protein expression and activated the MAPK pathway in RAW246.7 macrophages. Finally, GSP-2 induced the production of the cytokines TNFα, IL1β, and IL6. Our data demonstrated that GSP-2 was specifically recognized by TLR4, promoting cytokine secretion and immune modulation in macrophages. Public Library of Science 2019-08-23 /pmc/articles/PMC6707555/ /pubmed/31442262 http://dx.doi.org/10.1371/journal.pone.0221636 Text en © 2019 Liu et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Liu, Kai-Sheng Zhang, Cheng Dong, Hong-Liang Li, Kai-Kai Han, Quan-Bin Wan, Yong Chen, Rui Yang, Fang Li, Hai-Li Ko, Chun-Hay Han, Xiao-Qiang GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist |
title | GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist |
title_full | GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist |
title_fullStr | GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist |
title_full_unstemmed | GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist |
title_short | GSP-2, a polysaccharide extracted from Ganoderma sinense, is a novel toll-like receptor 4 agonist |
title_sort | gsp-2, a polysaccharide extracted from ganoderma sinense, is a novel toll-like receptor 4 agonist |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707555/ https://www.ncbi.nlm.nih.gov/pubmed/31442262 http://dx.doi.org/10.1371/journal.pone.0221636 |
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