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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Effects of human cyclooxygenase-2 gene silencing on synovial cells of rheumatoid arthritis mediated by lentivirus
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Effects of human cyclooxygenase-2 gene silencing on synovial cells of rheumatoid arthritis mediated by lentivirus

机译:人环氧基酶-2基因沉默对慢病毒介导的类风湿性关节炎滑膜细胞的影响

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The aim of the study is to screen the effective shRNA sequence which can silence the human COX-2 expression level in synovial cells of rheumatoid arthritis (RA) patient transfected by the lentivirus. Four pairs of hCOX-2 shRNA were designed and inserted into lentivirus to form pGPHI/GFP/Neo-shRNA vector. The reconstructed virus was transfected into synovial cells derived from RA patients, and then the expression level of hCOX-2 mRNA and the protein of the inflammatory factors including prostaglandin E2 (PGE2), vascular endothelial growth factor (VEGF), interleukin-1 beta (IL-1 beta) and tumour necrosis factor alpha (TNF-alpha) in the supernatants were examined with real-time PCR and ELISA, respectively. There was no obvious negative influence on cell growth and morphology after hCOX-2 shRNA gene transfection mediated by lentivirus. The hCOX-2 mRNA expression level, as well as the concentration of PGE2, VEGF, IL-1 beta and TNF-alpha, decreased significantly (p.05). RNAi mediated by lentivirus can significantly inhibit hCOX-2 mRNA expression level in synovial cells of RA patients, so as to reduce the expression of inflammatory cytokines.
机译:该研究的目的是筛选有效的ShRNA序列,其能够沉默于慢病毒转染的类风湿性关节炎(RA)患者的类风湿性关节炎(RA)患者的滑膜细胞中的人COX-2表达水平。设计并插入慢病毒的四对HCOX-2 shRNA以形成PGPHI / GFP / Neo-ShRNA载体。将重建的病毒转染到从RA患者衍生的滑膜细胞中,然后是HCOX-2 mRNA的表达水平和炎症因子的蛋白质,包括前列腺素E2(PGE2),血管内皮生长因子(VEGF),白细胞介素-1β(用实时PCR和ELISA检查上清液中的IL-1β)和肿瘤坏死因子α(TNF-α)。慢病毒介导的HCOX-2 shRNA基因转染后对细胞生长和形态没有明显的负面影响。 HCOX-2 mRNA表达水平以及PGE2,VEGF,IL-1β和TNF-α的浓度显着降低(P <.05)。由慢病毒介导的RNAi可以显着抑制RA患者的滑膜细胞中的HCOX-2 mRNA表达水平,从而减少炎症细胞因子的表达。

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