Proteoglycan from Bacillus sp. BS11 Inhibits the Inflammatory Response by Suppressing the MAPK and NF-κB Pathways in Lipopolysaccharide-Induced RAW264.7 Macrophages

被引:9
|
作者
Wang, Qingchi [1 ,2 ,3 ,4 ]
Liu, Weixiang [1 ,2 ,3 ,4 ]
Yue, Yang [1 ,2 ,3 ,4 ]
Sun, Chaomin [1 ,2 ,3 ,4 ]
Zhang, Quanbin [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Inst Oceanol, CAS Key Lab Expt Marine Biol, Qingdao 266071, Peoples R China
[2] Qingdao Natl Lab Marine Sci & Technol, Lab Marine Biol & Biotechnol, Qingdao 266071, Peoples R China
[3] Univ Chinese Acad Sci, Dept Earth Sci, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Ctr Ocean Megasci, Qingdao 266071, Peoples R China
关键词
Bacillus sp; proteoglycan; anti-inflammation; macrophages; ACTIVATED PROTEIN-KINASE; NITRIC-OXIDE SYNTHASE; POLYSACCHARIDE; MECHANISMS; TARGETS;
D O I
10.3390/md18120585
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Inflammation is involved in the pathogenesis of many debilitating diseases. Proteoglycan isolated from marine Bacillus sp. BS11 (EPS11) was shown to have anticancer activity, but its anti-inflammatory potential remains elusive. In the present study, the anti-inflammatory effects and mechanism of EPS11 were evaluated using a lipopolysaccharide (LPS)-induced RAW264.7 macrophage model. Biochemical characterization showed that the total sugar content and protein content of EPS11 were 49.5% and 30.2% respectively. EPS11 was composed of mannose, glucosamine, galactosamine, glucose, galactose, rhamnose, and glucuronic acid. Its molecular weight was determined to be 3.06 x 10(5) Da. The protein determination of EPS11 was also performed. EPS11 displayed a strong anti-inflammatory effect on LPS-stimulated RAW264.7 macrophages in vitro, which significantly suppressed inflammatory cytokines and mediators (such as NO, TNF-alpha, IL-6 and IL-1 beta, and COX-2). Western blot analysis indicated that EPS11 could downregulate the expression of many key proteins in mitogen-activated protein kinases (MAPKs) and transcription factor nuclear factor-kappa B (NF-kappa B) signaling pathways. In particular, EPS11 almost completely inhibited the expression of NF-kappa B P65, which indicated that EPS11 acted primarily on the NF-kappa B pathways. These findings offer new insights into the molecular mechanism underlying the anti-inflammatory effect of EPS11.
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页数:16
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