Hemolysate-induced Expression of Intercellular Adhesion Molecule-1 and Monocyte Chemoattractant Protein-1 Expression in Cultured Brain Microvascular Endothelial Cells via Through ROS-dependent NF-κB Pathways

被引:9
|
作者
Lu, Hua [1 ]
Shi, Ji-Xin [1 ]
Zhang, Dong-Mei [2 ,3 ]
Shen, Jie [2 ,3 ]
Lin, Yi-Xing [1 ]
Hang, Chun-Hua [1 ]
Yin, Hong-Xia [1 ]
机构
[1] Nanjing Univ, Sch Clin, Jinling Hosp, Dept Neurosurg, Nanjing 210002, Peoples R China
[2] Nanjing Univ, Coll Life Sci, Dept Biochem, Nanjing 210093, Peoples R China
[3] Nanjing Univ, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
Brain microvascular endothelial cells; Hemolysate; Inflammation; Intercellular adhesion molecule-1; Monocyte chemoattractant protein-1; NF-kappa B; Reactive oxygen species; SUBARACHNOID HEMORRHAGE; TRANSENDOTHELIAL MIGRATION; OXIDATIVE STRESS; PATHOGENESIS; INFLAMMATION; MECHANISMS; VASOSPASM; MCP-1;
D O I
10.1007/s10571-008-9300-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In order to determine the possible effects of hemolysate on brain microvascular endothelial cells (BMECs), we examined the effects of hemolysate on the expression of intercellular adhesion molecule-1 (ICAM-1) and monocyte chemoattractant protein-1 (MCP-1), generation of reactive oxygen species (ROS), and NF-kappa B activation in rat BMECs. Hemolysate induced the expression of ICAM-1 and MCP-1 in endothelial cells. In addition, hemolysate stimulated nuclear translocation of the p65 subunit of NF-kappa B, and NF-kappa B DNA-binding activity in BMECs. Furthermore, hemolysate increased ROS generation, and hemolysate-induced ICAM-1 and MCP-1 expression and NF-kappa B activation were abrogated in the presence of the direct scavenger of ROS. Taken together, our results indicate that hemolysate can induce inflammatory responses that increase expression of ICAM-1 and MCP-1, through ROS-dependent NF-kappa B activation in BMECs.
引用
收藏
页码:87 / 95
页数:9
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