A novel polysaccharide isolated from Coriolus versicolor polarizes M2 macrophages into an M1 phenotype and reversesits immunosuppressive effect on tumor microenvironment

被引:13
作者
Bi, Sixue [1 ]
Jing, Yongshuai [2 ]
Cui, Xuehui [1 ]
Gong, Yitong [3 ]
Zhang, Junli [4 ]
Feng, Xiaofei [4 ]
Shi, Zhen [3 ]
Zheng, Qiusheng [1 ]
Li, Defang [1 ,5 ]
机构
[1] Binzhou Med Univ, Sch Integrated Tradit Chinese & Western Med, Featured Lab Biosynth & Target Discovery Act Compo, Yantai 264003, Shandong, Peoples R China
[2] Hebei Univ Sci & Technol, Coll Chem & Pharmaceut Engn, Shijiazhuang 050018, Hebei, Peoples R China
[3] Binzhou Med Univ, Sch Basic Med Sci, Yantai 264003, Shandong, Peoples R China
[4] Binzhou Med Univ, Yantai Affiliated Hosp, Clin Med Coll 2, Yantai 264100, Shandong, Peoples R China
[5] Binzhou Med Univ, Sch Integrated Tradit Chinese & Western Med, Yantai 264003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Coriolus versicolor; Polysaccharide; M2; macrophages; GANODERMA-SINENSE POLYSACCHARIDE; STRUCTURAL-CHARACTERIZATION; CANCER; ACTIVATION; CELLS; LIPOPOLYSACCHARIDE; INFLAMMATION; MECHANISMS; IMMUNITY; AGONISTS;
D O I
10.1016/j.ijbiomac.2024.129352
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Converting M2 macrophages into an M1 phenotype in the tumor microenvironment, provides a new direction for tumor treatment. Here, we further report CVPW-1, a new polysaccharide of 1.03 x 106 Da that was isolated from Coriolus versicolor. Its monosaccharide was composed of mannose, glucose, and galactose at a ratio of 1.00:8.73:1.68. The backbone of CVPW-1 was composed of (1 -> 3) -linked alpha-D-Glcp residues and (1 -> 3,6)linked alpha-D-Glcp residues that branched at O-6. The branch consisted of (1 -> 6) -linked alpha-D-Glcp residues and (1 -> 4) -linked alpha-D-Glap, and some branches were terminated with (1 ->)-linked beta-D-Manp residues according to the results of HPLC, FT-IR, GC-MS, 1D and 2D NMR. Meanwhile, CVPW-1 could polarize M2 macrophages to M1 phenotypein vitro by binding to TLR4 and inducing the activation of Akt, JNK and NF-kappa B. This process involved reversing the functional inhibition of CD8+ T lymphocytes by inhibiting the expression of TREM2 in M2 macrophages. The in vivo experiments showed that oral administration of CVPW-1 could inhibit the growth of tumor in mice and polarize TAMs to M1 phenotype. Thus, the novel polysaccharide CVPW-1 from Coriolus versicolor might activate a variety of immune cells and then play an anti -tumor role. These results demonstrated that CVPW-1 could be developed as a potential immuno-oncology treatment reagent.
引用
收藏
页数:17
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