Histidine-rich glycoprotein inhibited high mobility group box 1 in complex with heparin-induced angiogenesis in matrigel plug assay

被引:33
作者
Wake, Hidenori [1 ]
Mori, Shuji [2 ]
Liu, Keyue [1 ]
Takahashi, Hideo K. [1 ]
Nishibori, Masahiro [1 ]
机构
[1] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Pharmacol, Okayama 7008558, Japan
[2] Shujitsu Univ, Sch Pharm, Okayama 7038516, Japan
基金
日本学术振兴会;
关键词
Angiogenesis; HMGB1; HRG; Heparin; ENDOTHELIAL GROWTH-FACTOR; NECROSIS-FACTOR-ALPHA; HUMAN-PLASMA PROTEIN; PLATELET THROMBOSPONDIN; LATE MEDIATOR; COLON-CANCER; TUMOR; BINDING; HMGB1; PROLINE;
D O I
10.1016/j.ejphar.2009.09.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Histidine-rich glycoprotein (HRG) is a heparin-binding glycoprotein present in plasma at 100 mu g/ml. A recent Study revealed that HRG Suppressed heparin-dependent basic fibroblast growth factor (bFGF)-induced angiogenesis. Additionally, we reported that hi.-h mobility group box 1 (HMGB1) in complex with heparin induces angiogenesis; therefore, we examined the effect of HRG oil heparin-dependent HMGB1-induced angiogenesis in the present study. HRG completely inhibited angiogenesis induced by HMGB1 in complex with heparin. HRG inhibited the diffusion of a complex of HMGB1 with heparin front matrigel into surrounding tissue. HRG also competed with HMGB1 for heparin binding in vitro. Moreover, HRG inhibited heparin-dependent vascular endothelial growth factor-A(165) (VEGF-A(165))-induced angiogenesis. These results Strongly suggested that HRG might be an inhibitor of angiogenesis induced by growth factors with heparin binding activity and that HRG may be a potential drug for angiogenic diseases, including tumor growth. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 95
页数:7
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