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pubmed-article:16023604pubmed:dateCreated2005-7-18lld:pubmed
pubmed-article:16023604pubmed:abstractTextWater-soluble proteoglycan (WSPG) of Agaricus blazei Murill has been known to stimulate the non-specific complements and humoral immune functions to act as polyclonal activators of B cells and to inhibit tumor growth and metastasis. However, little is known about its immunomodulating effects on murine bone marrow (BM)-derived dendritic cells (DC). In the present study, we examined the maturation process of murine BM-DC. BM cells were cultured in the presence of IL-4 and GM-CSF and the generated immature DC were stimulated with WSPG or LPS (WSPG-DC and LPS-DC, respectively) for 24 h. WSPG significantly enhanced the expression of co-stimulatory molecules (CD80 and CD86) and major histocompatibility complex (MHC) II, as did LPS. IL-12p70 production in WSPG-DC was also identical to that in LPS-DC. The antigen-uptake capacity of WSPG-DC was determined by FITC-labeled dextran uptake. WSPG-DC lost dextran uptake capacity comparable to LPS-DC. The antigen-presenting capacity of WSPG-DC as analyzed by allogeneic T cell proliferation was significantly increased in comparison with immature DC, was identical to LPS-DC, and induced higher levels of IL-2 in responding T cells. These results indicate the immunomodulatory properties of WSPG, which might be therapeutically useful in the control of cancers and immunodeficient diseases through the up-regulation of DC maturation.lld:pubmed
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pubmed-article:16023604pubmed:authorpubmed-author:ChoiIn-HakIHlld:pubmed
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pubmed-article:16023604pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16023604pubmed:articleTitleEffect of water-soluble proteoglycan isolated from Agaricus blazei on the maturation of murine bone marrow-derived dendritic cells.lld:pubmed
pubmed-article:16023604pubmed:affiliationDepartment of Microbiology and Medical Research Institute, Pusan National University, College of Medicine, Ami-dong 1-10, Seo-gu, Pusan 602-739, Republic of Korea.lld:pubmed
pubmed-article:16023604pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16023604pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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