Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells.
Reversing the function of immune suppressor cells may improve the efficacy of cancer therapy. Here, we have isolated a novel polysaccharide MPSSS (577.2 Kd) from Lentinus edodes and examined its effects on differentiation and function of myeloid-derived suppressor cells (MDSCs). MPSSS is composed of...
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2012-01-01
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doaj-165c6838e9c54e57bfaff065b9915c372020-11-24T21:20:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5175110.1371/journal.pone.0051751Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells.Hao WuNing TaoXiaoman LiuXiao LiJian TangChungwah MaXiaofei XuHaitao ShaoBaidong HouHui WangZhihai QinReversing the function of immune suppressor cells may improve the efficacy of cancer therapy. Here, we have isolated a novel polysaccharide MPSSS (577.2 Kd) from Lentinus edodes and examined its effects on differentiation and function of myeloid-derived suppressor cells (MDSCs). MPSSS is composed of glucose (75.0%), galactose (11.7%), mannose (7.8%), and xylose (0.4%). In vivo, it inhibits the growth of McgR32 tumor cells, which is correlated with a reduced percentage of MDSCs in peripheral blood. In vitro, it induces both morphological and biophysical changes in MDSCs. Importantly, MPSSS up-regulates MHC II and F4/80 expression on MDSCs, and reverses their inhibition effect on CD4(+) T cells in a dose-dependent manner. The mechanism study shows that MPSSS may stimulate MDSCs through a MyD88 dependent NF-κB signaling pathway. Together, we demonstrated for the first time that MPSSS stimulates the differentiation of MDSCs and reverses its immunosuppressive functions, shedding new light on developing novel anti-cancer strategies by targeting MDSCs.http://europepmc.org/articles/PMC3525656?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hao Wu Ning Tao Xiaoman Liu Xiao Li Jian Tang Chungwah Ma Xiaofei Xu Haitao Shao Baidong Hou Hui Wang Zhihai Qin |
spellingShingle |
Hao Wu Ning Tao Xiaoman Liu Xiao Li Jian Tang Chungwah Ma Xiaofei Xu Haitao Shao Baidong Hou Hui Wang Zhihai Qin Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. PLoS ONE |
author_facet |
Hao Wu Ning Tao Xiaoman Liu Xiao Li Jian Tang Chungwah Ma Xiaofei Xu Haitao Shao Baidong Hou Hui Wang Zhihai Qin |
author_sort |
Hao Wu |
title |
Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. |
title_short |
Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. |
title_full |
Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. |
title_fullStr |
Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. |
title_full_unstemmed |
Polysaccharide from Lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. |
title_sort |
polysaccharide from lentinus edodes inhibits the immunosuppressive function of myeloid-derived suppressor cells. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2012-01-01 |
description |
Reversing the function of immune suppressor cells may improve the efficacy of cancer therapy. Here, we have isolated a novel polysaccharide MPSSS (577.2 Kd) from Lentinus edodes and examined its effects on differentiation and function of myeloid-derived suppressor cells (MDSCs). MPSSS is composed of glucose (75.0%), galactose (11.7%), mannose (7.8%), and xylose (0.4%). In vivo, it inhibits the growth of McgR32 tumor cells, which is correlated with a reduced percentage of MDSCs in peripheral blood. In vitro, it induces both morphological and biophysical changes in MDSCs. Importantly, MPSSS up-regulates MHC II and F4/80 expression on MDSCs, and reverses their inhibition effect on CD4(+) T cells in a dose-dependent manner. The mechanism study shows that MPSSS may stimulate MDSCs through a MyD88 dependent NF-κB signaling pathway. Together, we demonstrated for the first time that MPSSS stimulates the differentiation of MDSCs and reverses its immunosuppressive functions, shedding new light on developing novel anti-cancer strategies by targeting MDSCs. |
url |
http://europepmc.org/articles/PMC3525656?pdf=render |
work_keys_str_mv |
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