摘要
提取人脐静脉内皮细胞经内毒素刺激 6h后的mRNA并合成cDNA ,与对照组进行抑制消减杂交 ,经菌落斑点杂交筛选出阳性克隆 ,进行测序和同源性分析 ,并采用Northern杂交验证新的cDNA序列。共获得 2 5条差异表达基因 ,涉及与编码炎症介质、胞内信号传导、细胞骨架、细胞凋亡和能量代谢相关的基因 ,其中 3条为新基因序列。结果表明 ,抑制消减杂交技术有效地克隆了内皮细胞内毒素刺激后相关基因 ,有助于阐明内毒素激活血管内皮细胞的机制 。
To screen genes in endothelial cells resulted from responding to lipopolysaccharide (LPS), mRNA was extracted from both untreated human umbilical endothelial cells (HUVEC) following and HUVEC which were treated with LPS for 6 hours. cDNAs of both populations were synthesized to generate cDNA libraries by suppression subtractive hybridization (SSH). The libraries were then screened with colony dot blots. Positive clones were sequenced and BLAST analysed. The results showed differential genes included 3 novel genes and 22 known genes. The 3 novel genes were confirmed by Northern blotting analysis. These 22 known genes were involved in the regulation of proinflammatory response, cell apoptosis, cytoskeleton, signal transduction and energy metabolism. These results suggest that SSH is an effective technique to detect differential gene expression in HUVEC, which may be helpful to evaluate molecular mechanisms of endothelial injury induced by LPS and provide potential therapeutic targets for LPS related disturbances.
出处
《解放军医学杂志》
CAS
CSCD
北大核心
2002年第4期336-338,共3页
Medical Journal of Chinese People's Liberation Army
基金
国家自然科学基金重点资助项目 (编号 39830 4 0 0 )