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从丛生大叶藻中提取、分离、结构表征及富含阿魏酸半乳糖醛酸聚糖的抗肿瘤特性

Extraction, Isolation, Structural Characterization and Anti-Tumor Properties of an Apigalacturonan-Rich Polysaccharide from the Sea Grass Zostera caespitosa Miki.

作者信息

Lv Youjing, Shan Xindi, Zhao Xia, Cai Chao, Zhao Xiaoliang, Lang Yinzhi, Zhu He, Yu Guangli

机构信息

Key Laboratory of Marine Drugs, Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.

Shandong Provincial Key Laboratory of Glycoscience and Glycotechnology, Ocean University of China, Qingdao 266003, China.

出版信息

Mar Drugs. 2015 Jun 11;13(6):3710-31. doi: 10.3390/md13063710.

Abstract

An apigalacturonan (AGA)-rich polysaccharide, ZCMP, was isolated from the sea grass Zostera caespitosa Miki. The depolymerized fragments derived from ZCMP were obtained by either acidic degradation or pectinase degradation, and their structures were characterized by electrospray ionization collision-induced-dissociation mass spectrometry (ESI-CID-MS2) and nuclear magnetic resonance (NMR) spectroscopy. The average molecular weight of ZCMP was 77.2 kD and it consisted of galacturonic acid (GalA), apiosefuranose (Api), galactose (Gal), rhamnose (Rha), arabinose (Ara), xylose (Xyl), and mannose (Man), at a molar ratio of 51.4꞉15.5꞉6.0꞉11.8꞉4.2꞉4.4꞉4.2. There were two regions of AGA (70%) and rhamnogalacturonan-I (RG-Ι, 30%) in ZCMP. AGA was composed of an α-1,4-D-galactopyranosyluronan backbone mainly substituted at the O-3 position by single Api residues. RG-Ι possessed a backbone of repeating disaccharide units of →4GalAα1,2Rhaα1→, with a few α-L-arabinose and β-D-galactose residues as side chains. The anti-angiogenesis assay showed that ZCMP inhibited the migratory activity of human umbilical vein endothelial cell (HUVECs), with no influence on endothelial cells growth. ZCMP also promoted macrophage phagocytosis. These findings of the present study demonstrated the potential anti-tumor activity of ZCMP through anti-angiogenic and immunoregulatory pathways.

摘要

从丛生大叶藻中分离出一种富含阿魏酸半乳糖醛酸聚糖(AGA)的多糖——ZCMP。通过酸性降解或果胶酶降解获得了源于ZCMP的解聚片段,并用电喷雾电离碰撞诱导解离质谱(ESI-CID-MS2)和核磁共振(NMR)光谱对其结构进行了表征。ZCMP的平均分子量为77.2 kD,它由半乳糖醛酸(GalA)、阿魏呋喃糖(Api)、半乳糖(Gal)、鼠李糖(Rha)、阿拉伯糖(Ara)、木糖(Xyl)和甘露糖(Man)组成,摩尔比为51.4∶15.5∶6.0∶11.8∶4.2∶4.4∶4.2。ZCMP中有两个区域,即AGA(70%)和鼠李糖半乳糖醛酸聚糖-I(RG-I,30%)。AGA由α-1,4-D-吡喃半乳糖醛酸聚糖主链组成,主要在O-3位被单个Api残基取代。RG-I具有→4GalAα1,2Rhaα1→的重复二糖单元主链,有一些α-L-阿拉伯糖和β-D-半乳糖残基作为侧链。抗血管生成试验表明,ZCMP抑制人脐静脉内皮细胞(HUVECs)的迁移活性,对内皮细胞生长无影响。ZCMP还促进巨噬细胞吞噬作用。本研究的这些发现证明了ZCMP通过抗血管生成和免疫调节途径具有潜在的抗肿瘤活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e86/4483652/1f996c607ee7/marinedrugs-13-03710-g001.jpg

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