中华神经外科疾病研究杂志
中華神經外科疾病研究雜誌
중화신경외과질병연구잡지
Chinese Journal of Neurosurgical Disease Research
2015年
4期
302-306
,共5页
张磊%罗玉玉%常鹏飞%孙世中
張磊%囉玉玉%常鵬飛%孫世中
장뢰%라옥옥%상붕비%손세중
锌指核转录因子%内皮型一氧化氮合酶%脑血管痉挛
鋅指覈轉錄因子%內皮型一氧化氮閤酶%腦血管痙攣
자지핵전록인자%내피형일양화담합매%뇌혈관경련
ZNF580%eNOS%Cerebral angiospasm
目的:研究血管内皮细胞中锌指核转录因子( ZNF580)对内皮型一氧化氮合酶( eNOS)表达的影响。方法通过基因芯片技术检测ZNF580过表达的人血管内皮杂交瘤细胞系(EA.hy926)中基因表达谱的变化。采用实时定量聚合酶链反应(RT-PCR)和免疫印迹试验(Western bolt)检测转染了携带有ZNF580的慢病毒载体(Lenti-GFP-ZNF580)和携带ZNF580小干扰RNA慢病毒载体(Lenti-RNAi-ZNF580)的EA.hy926中ZNF580和eNOS mRNA和蛋白的表达变化。结果多种基因表达在ZNF580过表达的EA.hy926细胞中发生了改变,其中eNOS等基因的表达明显上调。转染了携带有(Lenti-RNAi-ZNF580)的内皮细胞中ZNF580和eNOS表达显著下调,而转染了Lenti -GFP-ZNF580的内皮细胞中ZNF580和eNOS表达显著上调。结论转录因子ZNF580促进了血管内皮细胞中eNOS的表达。
目的:研究血管內皮細胞中鋅指覈轉錄因子( ZNF580)對內皮型一氧化氮閤酶( eNOS)錶達的影響。方法通過基因芯片技術檢測ZNF580過錶達的人血管內皮雜交瘤細胞繫(EA.hy926)中基因錶達譜的變化。採用實時定量聚閤酶鏈反應(RT-PCR)和免疫印跡試驗(Western bolt)檢測轉染瞭攜帶有ZNF580的慢病毒載體(Lenti-GFP-ZNF580)和攜帶ZNF580小榦擾RNA慢病毒載體(Lenti-RNAi-ZNF580)的EA.hy926中ZNF580和eNOS mRNA和蛋白的錶達變化。結果多種基因錶達在ZNF580過錶達的EA.hy926細胞中髮生瞭改變,其中eNOS等基因的錶達明顯上調。轉染瞭攜帶有(Lenti-RNAi-ZNF580)的內皮細胞中ZNF580和eNOS錶達顯著下調,而轉染瞭Lenti -GFP-ZNF580的內皮細胞中ZNF580和eNOS錶達顯著上調。結論轉錄因子ZNF580促進瞭血管內皮細胞中eNOS的錶達。
목적:연구혈관내피세포중자지핵전록인자( ZNF580)대내피형일양화담합매( eNOS)표체적영향。방법통과기인심편기술검측ZNF580과표체적인혈관내피잡교류세포계(EA.hy926)중기인표체보적변화。채용실시정량취합매련반응(RT-PCR)화면역인적시험(Western bolt)검측전염료휴대유ZNF580적만병독재체(Lenti-GFP-ZNF580)화휴대ZNF580소간우RNA만병독재체(Lenti-RNAi-ZNF580)적EA.hy926중ZNF580화eNOS mRNA화단백적표체변화。결과다충기인표체재ZNF580과표체적EA.hy926세포중발생료개변,기중eNOS등기인적표체명현상조。전염료휴대유(Lenti-RNAi-ZNF580)적내피세포중ZNF580화eNOS표체현저하조,이전염료Lenti -GFP-ZNF580적내피세포중ZNF580화eNOS표체현저상조。결론전록인자ZNF580촉진료혈관내피세포중eNOS적표체。
Objective The effect of the novel zinc-finger nuclear transcription factor ( ZNF580 ) on the expression of endothelial nitric oxide synthase ( eNOS) in vascular endothelial cells is discussed.Methods The changes of gene expression profiling of ZNF580-overexpressed EA.hy926 cells were detected by gene microarray.The ZNF580 and eNOS expressions of the EA.hy926 endothelial cells which transfected with Lenti-GFP-ZNF580 and Lenti-RNAi-ZNF580 were detected by the real-time polymerase chain reaction (RT-PCR) and Western bolt.Results The results of gene chip showed that there were many gene expression changes in ZNF580-overexpressed EA.hy926 cells. The expression of eNOS was markedly up-regulated.The mRNA and protein expressions of ZNF580 and eNOS were increased in EA.hy926 cells transfected with Lenti-GFP-ZNF580.But the eNOS and ZNF580 expressions were down-regulated in EA.hy926 cells transfected with Lenti-RNAi-ZNF580.Conclusion Transcriptional factor ZNF580 promotes the expression of eNOS in vascular endothelial cells.