Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.

Ginseng extract has been shown to possess certain anti-virus, anti-tumor and immune-activating effects. However, the immunostimulatory effect of ginseng berry extract (GB) has been less well characterized. In this study, we investigated the effect of GB on the activation of mouse dendritic cells (DC...

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Main Authors: Wei Zhang, Si-Young Cho, Gao Xiang, Kyung-Jin Min, Qing Yu, Jun-O Jin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4474810?pdf=render
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spelling doaj-45206c4a60814faea3de7ec226bcb16a2020-11-25T02:34:03ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01106e013092610.1371/journal.pone.0130926Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.Wei ZhangSi-Young ChoGao XiangKyung-Jin MinQing YuJun-O JinGinseng extract has been shown to possess certain anti-virus, anti-tumor and immune-activating effects. However, the immunostimulatory effect of ginseng berry extract (GB) has been less well characterized. In this study, we investigated the effect of GB on the activation of mouse dendritic cells (DCs) in vitro and in vivo. GB treatment induced up-regulation of co-stimulatory molecules in bone marrow-derived DCs (BMDCs). Interestingly, GB induced a higher degree of co-stimulatory molecule up-regulation than ginseng root extract (GR) at the same concentrations. Moreover, in vivo administration of GB promoted up-regulation of CD86, MHC class I and MHC class II and production of IL-6, IL-12 and TNF-α in spleen DCs. GB also promoted the generation of Th1 and Tc1 cells. Furthermore, Toll like receptor 4 (TLR4) and myeloid differentiation primary response 88 (MyD88) signaling pathway were essential for DC activation induced by GB. In addition, GB strongly prompted the proliferation of ovalbumin (OVA)-specific CD4 and CD8 T cells. Finally, GB induced DC activation in tumor-bearing mice and the combination of OVA and GB treatment inhibited B16-OVA tumor cell growth in C57BL/6 mice. These results demonstrate that GB is a novel tumor therapeutic vaccine adjuvant by promoting DC and T cell activation.http://europepmc.org/articles/PMC4474810?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Wei Zhang
Si-Young Cho
Gao Xiang
Kyung-Jin Min
Qing Yu
Jun-O Jin
spellingShingle Wei Zhang
Si-Young Cho
Gao Xiang
Kyung-Jin Min
Qing Yu
Jun-O Jin
Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.
PLoS ONE
author_facet Wei Zhang
Si-Young Cho
Gao Xiang
Kyung-Jin Min
Qing Yu
Jun-O Jin
author_sort Wei Zhang
title Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.
title_short Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.
title_full Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.
title_fullStr Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.
title_full_unstemmed Ginseng Berry Extract Promotes Maturation of Mouse Dendritic Cells.
title_sort ginseng berry extract promotes maturation of mouse dendritic cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Ginseng extract has been shown to possess certain anti-virus, anti-tumor and immune-activating effects. However, the immunostimulatory effect of ginseng berry extract (GB) has been less well characterized. In this study, we investigated the effect of GB on the activation of mouse dendritic cells (DCs) in vitro and in vivo. GB treatment induced up-regulation of co-stimulatory molecules in bone marrow-derived DCs (BMDCs). Interestingly, GB induced a higher degree of co-stimulatory molecule up-regulation than ginseng root extract (GR) at the same concentrations. Moreover, in vivo administration of GB promoted up-regulation of CD86, MHC class I and MHC class II and production of IL-6, IL-12 and TNF-α in spleen DCs. GB also promoted the generation of Th1 and Tc1 cells. Furthermore, Toll like receptor 4 (TLR4) and myeloid differentiation primary response 88 (MyD88) signaling pathway were essential for DC activation induced by GB. In addition, GB strongly prompted the proliferation of ovalbumin (OVA)-specific CD4 and CD8 T cells. Finally, GB induced DC activation in tumor-bearing mice and the combination of OVA and GB treatment inhibited B16-OVA tumor cell growth in C57BL/6 mice. These results demonstrate that GB is a novel tumor therapeutic vaccine adjuvant by promoting DC and T cell activation.
url http://europepmc.org/articles/PMC4474810?pdf=render
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