Polysaccharide from Lentinus edodes Inhibits the Immunosuppressive Function of Myeloid-Derived Suppressor Cells

被引:42
作者
Wu, Hao [2 ]
Tao, Ning [3 ]
Liu, Xiaoman [3 ]
Li, Xiao [3 ]
Tang, Jian [4 ]
Ma, Chungwah [4 ]
Xu, Xiaofei [4 ]
Shao, Haitao [1 ]
Hou, Baidong [1 ]
Wang, Hui [2 ]
Qin, Zhihai [3 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Key Lab Infect & Immun, Beijing 100080, Peoples R China
[2] Xinxiang Med Univ, Xinxiang, Peoples R China
[3] Chinese Acad Sci, Inst Biophys, Prot & Peptide Pharmaceut Lab, Beijing 100080, Peoples R China
[4] Infinitus China Co Ltd, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
ANTITUMOR-ACTIVITY; IMMUNE-RESPONSES; CANCER-PATIENTS; DIFFERENTIATION; INTERLEUKIN-4; POLARIZATION; EXPANSION; IMPROVES; MICE;
D O I
10.1371/journal.pone.0051751
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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-kappa B 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.
引用
收藏
页数:9
相关论文
共 27 条
[1]   Increased production of immature myeloid cells in cancer patients: A mechanism of immunosuppression in cancer [J].
Almand, B ;
Clark, JI ;
Nikitina, E ;
van Beynen, J ;
English, NR ;
Knight, SC ;
Carbone, DP ;
Gabrilovich, DI .
JOURNAL OF IMMUNOLOGY, 2001, 166 (01) :678-689
[2]   INHIBITION OF MOUSE SARCOMA 180 BY POLYSACCHARIDES FROM LENTINUS EDODES (BERK) SING [J].
CHICHARA, G ;
MAEDA, Y ;
HAMURO, J ;
SASAKI, T ;
FUKUOKA, F .
NATURE, 1969, 222 (5194) :687-&
[3]  
CHIHARA G, 1970, CANCER RES, V30, P2776
[4]   Mechanisms and functional significance of tumour-induced dendritic-cell defects [J].
Gabrilovich, D .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (12) :941-952
[5]   The terminology issue for myeloid-derived suppressor cells [J].
Gabrilovich, Dmitry I. ;
Bronte, Vincenzo ;
Chen, Shu-Hsia ;
Colombo, Mario P. ;
Ochoa, Augusto ;
Ostrand-Rosenberg, Suzanne ;
Schreiber, Hans .
CANCER RESEARCH, 2007, 67 (01) :425-425
[6]   Tumors induce a subset of inflammatory monocytes with immunosuppressive activity on CD8+ T cells [J].
Gallina, Giovanna ;
Dolcetti, Luigi ;
Serafini, Paolo ;
De Santo, Carmela ;
Marigo, Ilaria ;
Colombo, Mario P. ;
Basso, Giuseppe ;
Brombacher, Frank ;
Borrello, Ivan ;
Zanovello, Paola ;
Bicciato, Silvio ;
Bronte, Vincenzo .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (10) :2777-2790
[7]   Myeloid-derived suppressor cell activation by combined LPS and IFN-γ treatment impairs DC development [J].
Greifenberg, Verena ;
Ribechini, Eliana ;
Roessner, Susanne ;
Lutz, Manfred B. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2009, 39 (10) :2865-2876
[8]  
HAMURO J, 1980, IMMUNOLOGY, V39, P551
[9]   Early exposure of high-dose interleukin-4 to tumor stroma reverses myeloid cell-mediated T-cell suppression [J].
Jiang, J. ;
Wang, Z. ;
Li, Z. ;
Zhang, J. ;
Wang, C. ;
Xu, X. ;
Qin, Z. .
GENE THERAPY, 2010, 17 (08) :991-999
[10]   Effect of the degree of sulfation on the physicochemical and biological properties of Pleurotus eryngii polysaccharides [J].
Jung, Ho Young ;
Bae, In Young ;
Lee, Suyong ;
Lee, Hyeon Gyu .
FOOD HYDROCOLLOIDS, 2011, 25 (05) :1291-1295