| 注册
首页|期刊导航|中国病理生理杂志|p38/ATF-2通路参与 C 反应蛋白诱导的内皮细胞活化

p38/ATF-2通路参与 C 反应蛋白诱导的内皮细胞活化

刘少军 李沅美 刘慰华 熊龙根 刘世明

中国病理生理杂志Issue(5):808-811,4.
中国病理生理杂志Issue(5):808-811,4.DOI:10.3969/j.issn.1000-4718.2015.05.007

p38/ATF-2通路参与 C 反应蛋白诱导的内皮细胞活化

p38 MAPK/ATF-2 pathway is involved in C-relative protein-induced en-dothelial cell activation

刘少军 1李沅美 2刘慰华 1熊龙根 1刘世明1

作者信息

  • 1. 广州医科大学附属第二医院广州心血管疾病研究所/心内科,广东广州510260
  • 2. 广东药学院生命科学与生物制药学院,广东广州510006
  • 折叠

摘要

Abstract

AIM:To investigate the role of p38 MAPK/ATF-2 pathway in C-relative protein ( CRP)-induced endothelial cell activation.METHODS:Human coronary artery endothelial cells ( HCAEC) were cultured and were used between passages 3 and 7.CRP served as a stimulus for endothelial cell activation.Western blotting was performed to de-termine the expression and phosphorylation of eNOS, p38 and ATF2.ELISA was carried out to detect the levels of ICAM-1, VCAM-1 and MCP-1 released from HCAEC.Pharmacological p38 inhibitors SB203580 and SB202190 were used to de-termine the effect of p38/ATF-2 pathway.RESULTS:CRP reduced the p-eNOS level in a concentration-dependent man-ner and induced the release of ICAM-1, VCAM-1 and MCP-1.The p38/ATF-2 pathway was activated by CRP treatment. SB203580 and SB202190 partially rescued p-eNOS level and suppressed the secretion of ICAM-1, VCAM-1 and MCP-1. CONCLUSION:p38MAPK/ATF-2 pathway participates in CRP-induced endothelial activation.

关键词

p38 MAPK/ATF-2通路/C反应蛋白/内皮细胞活化/动脉粥样硬化

Key words

p38 MAPK/ATF-2 pathway/C-relative protein/Endothelial activation/Atherosclerosis

分类

医药卫生

引用本文复制引用

刘少军,李沅美,刘慰华,熊龙根,刘世明..p38/ATF-2通路参与 C 反应蛋白诱导的内皮细胞活化[J].中国病理生理杂志,2015,(5):808-811,4.

基金项目

国家自然科学基金资助项目(No.81300151);广东省自然科学基金重点项目 ()

中国病理生理杂志

OA北大核心CSCDCSTPCD

1000-4718

访问量0
|
下载量0
段落导航相关论文