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Mechanism of macrophage activation induced by β-glucan produced from Paenibacillus polymyxa JB115
被引:29
|作者:
Chang, Zhi-Qiang
Lee, Joong-Su
Gebru, Elias
Hong, Joo-Heon
[2
]
Jung, Hee-Kyung
[2
]
Jo, Woo-Sik
[3
]
Park, Seung-Chun
[1
]
机构:
[1] Kyungpook Natl Univ, Dept Pharmacol, Coll Vet Med, Taegu 702701, South Korea
[2] Bio Ind Ctr, Taegu 704701, South Korea
[3] Gyeongbuk Agr Technol Adm, Agr Environm Dept, Taegu 702708, South Korea
关键词:
beta-Glucan;
Macrophage;
MAPKs;
NF kappa B;
NITRIC-OXIDE PRODUCTION;
TUMORICIDAL ACTIVITY;
IMMUNE RECOGNITION;
PROTEIN-KINASE;
SYNTHASE GENE;
POLYSACCHARIDE;
LIPOPOLYSACCHARIDE;
INDUCTION;
ANTITUMOR;
CANCER;
D O I:
10.1016/j.bbrc.2009.12.064
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:
beta-Glucans are heterogeneous groups of glucose polymers found in the cell walls of fungi, plants and some bacteria. Our previous report showed that a novel beta-1,3/1,6-glucan produced from Paenibacillus (P.) polymyxa JB115 can induce nitric oxide (NO) production in RAW264.7 cells. In the present study, the P-glucan significantly increased luciferase activity in cells transfected with NF kappa B or AP1, but not STAT1, reporter vector DNA, which contain their binding promoter site. All specific NF kappa B and MAPKs pathway inhibitors (pyrrolidine dithiocarbamate, AG490, U0126, SB203580 and SP600125) remarkably attenuated NO production induced by the beta-glucan. Furthermore, Western blot analysis revealed that the stimulation of Raw264.7 cells by beta-glucan induced phosphorylation of I kappa B and the consequent translocation of NF kappa B into the nucleus. Meanwhile, phosphorylation of ERK1/2, JNK/SAPK and p38 MAPKs in cytoplasm were also confirmed. All these results indicated that beta-glucan from P. polymyxa JB115 activates macrophages through MAPKs and NF kappa B signaling pathway. (C) 2009 Elsevier Inc. All rights reserved.
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页码:1358 / 1362
页数:5
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