Augmentation of LPS-induced vascular endothelial cell growth factor production in macrophages by transforming growth factor-β1

被引:16
|
作者
Koide, Naoki [1 ]
Odkhuu, Erdenezaya [1 ]
Naiki, Yoshikazu [1 ]
Tsolmongyn, Bilegtsaikhan [1 ]
Ito, Kiyoaki [1 ]
Komatsu, Takayuki [1 ]
Yoshida, Tomoaki [1 ]
Yokochi, Takashi [1 ]
机构
[1] Aichi Med Univ, Dept Microbiol & Immunol, Sch Med, Nagakute, Aichi 4801195, Japan
关键词
Lipopolysaccharide; transforming growth factor-1; vascular endothelial cell growth factor; macrophage; NITRIC-OXIDE; MURINE MACROPHAGES; GENE-EXPRESSION; VEGF; ANGIOGENESIS; HYPOXIA; INHIBITION; ACTIVATION;
D O I
10.1177/1753425913509291
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
The effect of LPS on the production of vascular endothelial growth factor (VEGF) was examined using RAW 264.7 macrophage cells. LPS induced VEGF production in RAW 264.7 cells and mouse peritoneal cells. LPS induced VEGF production via the expression of hypoxia inducible factor-1 alpha and LPS-induced VEGF production was dependent on the activation of p38 MAPK and NF-kappa B activation Transforming growth factor (TGF)-beta 1 augmented LPS-induced VEGF production, although TGF-beta 1 alone did not induce VEGF production. The augmentation of LPS-induced VEGF production by TGF-beta 1 was inhibited by a p38 MAPK inhibitor and was correlated with the phosphorylation of Smad3. The enhancing effect of TGF-beta 1 on LPS-induced VEGF production was observed invivo in the skin lesions of mice receiving a subcutaneous injection of LPS. Taken together, it is suggested that LPS induced the VEGF production in macrophages and that it was augmented by TGF-beta 1 invitro and invivo.
引用
收藏
页码:816 / 825
页数:10
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