Structural characterization of a polysaccharide from Coreopsis tinctoria Nutt. and its function to modify myeloid derived suppressor cells

被引:21
作者
Zhang, Wen-Sheng [1 ]
Sun, Qi-Li [2 ,3 ]
Zheng, Wei [1 ]
Zhang, Yuan [4 ]
Du, Juan [3 ]
Dong, Cai-Xia [2 ]
Tao, Ning [1 ]
机构
[1] Chinese Acad Sci, Inst Biophys, Key Lab Prot & Peptide Pharmaceut, Datun Rd 15, Beijing, Peoples R China
[2] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therape, Tianjin 300070, Peoples R China
[3] Jiamusi Univ, Coll Pharm, Dept Pharmacognosy, Jiamusi 154007, Peoples R China
[4] Beijing Univ Chinese Med, Sch Chinese Mat Med, Beijing 100102, Peoples R China
基金
中国国家自然科学基金;
关键词
Coreopsis tinctoria Nutt; Polysaccharide; Structure; Myeloid derived suppressor cells; T cells; CANCER STAGE; CORRELATE;
D O I
10.1016/j.ijbiomac.2019.01.002
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
Coreopsis tinctoria Nutt. (C tinctoria) is a natural plant with many health benefits, such as clearing heat and toxic materials. In this study, we investigate the effect of a polysaccharide from C tinctoria, aiming at improving the tumor microenvironment, which is associated with non-resolving inflammation. Through combining ion exchange and gel permeation chromatography, a polysaccharide named CTAP-3 is purified from the crude polysaccharides of C. tinctoria. The structure of CTAP-3 is characterized through high-performance gel permeation chromatography, chemical derivative analyses, GC-MS, FT-IR, and NMR. Results reveal that CTAP-3 consists of predominant amounts (87.2%) of galacturonic acid (GalA) residues, small amounts of arabinose (Ara) and rhamnose (Rham), and trace amounts of galactose (Gal). CTAP-3 is deduced to be native pectin-type polysaccharide containing a homo-galacturanan backbone consisting of alpha-(1 -> 4)-linked GalAp and methyl-esterified alpha-(1 -> 4)-linked GalAp residues in the ratio of 4:1. When myeloid-derived suppressor cells (MDSCs) are treated by CTAP-3, its suppressive effect on T cell proliferation is impaired. This result indicates that CTAP-3 is a candidate drug for improving the tumor microenvironment. (C) 2019 Published by Elsevier B.V.
引用
收藏
页码:926 / 933
页数:8
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