摘要
目的 :研究P38信号通路 (P38mitogen activatedproteinki nase ,P38MAPK)在人脐静脉内皮细胞表达P 选择素以及糖尿病动脉粥样硬化中的作用。方法 :分别以高葡萄糖、糖基化终产物 (AGE)、高胰岛素和过氧化氢刺激人脐静脉内皮细胞系ECV 30 4 ,再以P38MAPK特异性抑制剂SB2 0 35 80预处理 ,观察ECV 30 4细胞系中磷酸化P38MAPK和P 选择素的表达。结果 :4种刺激因素均可单独激活P38MAPK ,使磷酸化P38MAPK表达量明显增加 ,P 选择素表达量也明显增加 ;以SB2 0 35 80预处理后 ,P 选择素的表达被明显抑制。结论 :P38MAPK是P 选择素的上游信号分子 。
AIM: To investigate the role of P38 mitogen activated protein kinase (P38MAPK) in expression of P selectin on human umbilical vein endothelial cells and diabetic atherosclerosis. METHODS: Human umbilical vein endothelial cell line ECV304 were stimulated with high glucose, advanced glycosylation end products (AGE), high insulin and H 2O 2 respectively , and then expression of phosphorylated P38MAPK and P selectin was detected after being pre treated with SB203580 (P38MAPK specific inhibitor). RESULTS: High glucose, AGE, high insulin and H 2O 2 could activate P38MAPK by oneself, and increased notably expression of phosphorylated P38MAPK and P selectin on cell line ECV304; Expression of P selectin was inhibited significantly by SB203580. CONCLUSION: P38MAPK can regulate the expression of P selectin, P38MAPK is an upstream signaling molecule and also may be one of initial signals on atherosclerosis occurrence.
出处
《细胞与分子免疫学杂志》
CAS
CSCD
北大核心
2003年第3期291-293,共3页
Chinese Journal of Cellular and Molecular Immunology
基金
国家自然科学基金资助项目 (No .39570 344)