Water extract of Cordyceps militaris enhances maturation of murine bone marrow-derived dendritic cells in vitro

被引:35
作者
Kim, GY [1 ]
Ko, WS
Lee, JY
Lee, JO
Ryu, CH
Choi, BT
Park, YM
Jeong, YK
Lee, KJ
Choi, KS
Heo, MS
Choi, YH
机构
[1] Jeju Natl Univ, Coll Ocean Sci, Sch Appl Marine Sci, Jejudo 690756, South Korea
[2] Clin Res Ctr Oriental Med, Pusan 614052, South Korea
[3] Dong Eui Univ, Coll Oriental Med, Dept Oriental Med, Pusan 614052, South Korea
[4] Pusan Natl Univ, Coll Nat Sci, Dept Microbiol, Pusan 614714, South Korea
[5] Gyeongsang Natl Univ, Div Appl Life Sci, Jinju 660701, South Korea
[6] Pusan Natl Univ, Coll Med, Dept Microbiol & Immunol, Pusan 602739, South Korea
[7] Dong Eui Univ, Dept Microbiol, Pusan 609735, South Korea
关键词
Cordyceps militaris; proteoglycan; dendritic cell; cytotoxic T lymphocyte; P815; mastocytoma;
D O I
10.1248/bpb.29.354
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Water extract (WE) of Cordyceps militaris has been reported to produce antitumor and immunomodulatory activities in vivo and in vitro. However. the therapeutic mechanism has not been known. In this study, we investigated whether water extract of C. militaris induces the phenotypic and functional maturation of dendritic cells (DC). It profoundly increased CD40, CD54, CD80, CD86, and MHC class II expression in murine bone marrow (BM)-derived myeloid DC. Endocytosis was assessed by the uptake of FITC-dextran and FITC-albumin. The ability of unstimulated DC (UT-DC) to uptake dextran and albumin was higher than that of WE- or LPS-stimulated DC (LPS-DC). Also, UT-DC secreted a low concentration of IL-12, while WE- or LPS-DC secreted higher levels of IL-12 than UT-DC. WE not only formed morphologically mature DC and clusters, but also induced predominantly functional maturation. Moreover, WE is shown to promote the cytotoxicity of specific-cytotoxic T lymphocyte (CTL) induced by DC which were pulsed with P815 tumor-lysate during the stage of antigen presentation. These results suggest that DC maturation by WE can play a critical role in the improvement of the immunoregulatory function in patients with impaired host defence.
引用
收藏
页码:354 / 360
页数:7
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