摘要
目的:探讨炎症刺激因子TNF-α介导炎症时上调血管内皮细胞Tie2基因的机制。方法:采用RT-PCR、定量PCR以及Western blotting方法检测TNF-α作用于原代人主动脉内皮细胞株(HAECs)、原代人肺动脉内皮细胞株(HPAECs)时Tie2基因及ETS转录因子mRNA及蛋白的表达。结果:TNF-α可增加血管内皮细胞Tie2基因的表达。TNF-α不能增加内皮细胞HAECs和HPAECs的NERF-2、ELF表达;TNF-α刺激后约24h第1次检测到ESE-1 mRNA表达。延长刺激作用时间后,发现在18-36h之间可测到ESE-1 mRNA表达,24h为高峰,而蛋白质表达在18h极弱,36h达峰值。检测中所观察到ESE-1表达在Tie2表达之前且表达模式类似。结论:Tie2基因在TNF-α刺激时的上调与NERF-2或ELF介导无关,ESE-1可能在炎症因子刺激后Tie2的转录调节中起作用。
AIM: To explore the mechanism of tyrosine kinase receptors with immunoglobulin and EGF homology domains receptors 2 (Tie 2) gene up - regulation in vascular endothelial cell induced by TNF -α. METHODS: By applying with RT - PCR, quantitative PCR and Western blotting, mRNA and protein expressions of Tie 2 and some ETS transcription factors were detected in primary human aortic endothelial cells (HAECs) and primary human pulmonary artery endothelial cells (HPAECs). ResULTS : TNF -α increased the expression of Tie 2 in vascular endothelium cells. TNF -α did not increase the expression of New ETS related factor- 2 (NERF -2) and E74 -like factor- 1 (ELF1) in HAECs and HPAECs. ESE - 1 mRNA began to increase at 24 h. After extending stimulation time, it was found that ESE - 1 mRNA was detected at 18 -36 h and the peak was at 24 h, while protein expression was very weak at 18 h, and the peak was at 36 h. The expression of ESE - 1 occurred before Tie 2 expression and the mode was similar. CONCLUSION : Tie 2 gene is not related to up - regulation of NERF - 2 or ELF when stimulated with TNF -α. ESE - 1 may play a role in transcription regulation of Tie 2 after inflammation.
出处
《中国病理生理杂志》
CAS
CSCD
北大核心
2007年第5期880-883,共4页
Chinese Journal of Pathophysiology
基金
留学回国人员科研启动基金资助项目(No.2005)
广东省自然科学基金资助项目(No.5100992)
关键词
肿瘤坏死因子
基因
TIE
2
内皮细胞
转录因子
Tumor necrosis factor
Genes, Tie 2
Endothelial cells
Transcription factors