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党参果胶多糖的结构表征及其体内外免疫调节活性

Structural characterization of a pectic polysaccharide from Codonopsis pilosula and its immunomodulatory activities in vivo and in vitro.

作者信息

Zhang Pei, Hu Linhai, Bai Ruibin, Zheng Xiaoping, Ma Yuling, Gao Xia, Sun Bolu, Hu Fangdi

机构信息

School of Pharmacy, Lanzhou University, Lanzhou, 730000, China.

Spine surgery, First people's Hospital of Jiayuguan City, Jiayuguan, 735100, China.

出版信息

Int J Biol Macromol. 2017 Nov;104(Pt A):1359-1369. doi: 10.1016/j.ijbiomac.2017.06.023. Epub 2017 Jun 6.

Abstract

A pectic polysaccharide (named as CPP1c) extracted from Codonopsis pilosula was evaluated for its structural features and potential of immune-modulating activities in an aging mouse model of senescence accelerated mouse prone 8 (SAMP8) in vitro and in vivo. The relative molecular weight and the absolute molecular weight of CPP1c were 1.26×10Da and 1.49×10Da, respectively. Investigation of structural features by a combination of chemical and instrumental analysis showed CPP1c was composed of →1)-α-l-Rhap-(2,4→, →1)-α-l-Araf-(5→, →1)-α-d-Galp-(6→ and →1)-α-d-GalpA-(4→ in a molar ratio of 3:1:2:33. CPP1c could promote lymphocyte proliferation, modulate the percentage of CD4, CD8, CD28 and CD152 T cells and enhance the production of IL-2, TNF-α and IFN-γ. Moreover, PCR assay revealed CPP1c augmented the expressions of CD28, PI3K and p38MAPK mRNA, and the increase of protein expressions of the same genes was also confirmed by western blot analyses. In addition, CPP1c had the potential of promoting the homing of lymphocytes. Taking all factors into consideration, we deduced CPP1c might exert its immunostimulating potency via promoting T cell activation by TCR/CD28 signaling pathways.

摘要

从党参中提取的一种果胶多糖(命名为CPP1c),在体外和体内衰老加速小鼠易感8(SAMP8)衰老小鼠模型中,对其结构特征和免疫调节活性潜力进行了评估。CPP1c的相对分子量和绝对分子量分别为1.26×10Da和1.49×10Da。通过化学和仪器分析相结合的方法对其结构特征进行研究表明,CPP1c由→1)-α-L-鼠李糖基-(2,4→、→1)-α-L-阿拉伯糖基-(5→、→1)-α-D-半乳糖基-(6→和→1)-α-D-半乳糖醛酸基-(4→组成,摩尔比为3:1:2:33。CPP1c可促进淋巴细胞增殖,调节CD4、CD8、CD28和CD152 T细胞的百分比,并增强IL-2、TNF-α和IFN-γ的产生。此外,PCR检测显示CPP1c增强了CD28、PI3K和p38MAPK mRNA的表达,蛋白质印迹分析也证实了相同基因蛋白质表达的增加。此外,CPP1c具有促进淋巴细胞归巢的潜力。综合考虑所有因素,我们推断CPP1c可能通过TCR/CD28信号通路促进T细胞活化来发挥其免疫刺激效力。

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