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首页> 外文期刊>Chinese science bulletin >Inhibitory effect of a modified adenovirus type 5 E1 A gene on the NF-κB activity in porcine aortic endothelial cells induced by TNF-α
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Inhibitory effect of a modified adenovirus type 5 E1 A gene on the NF-κB activity in porcine aortic endothelial cells induced by TNF-α

机译:修饰的5 E1 A型腺病毒基因对TNF-α诱导的猪主动脉内皮细胞NF-κB活性的抑制作用

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摘要

The transcription factor nuclear factor κB (NF-κB) plays a key role in the delayed xenograft rejection (DXR). One of the important objects in the field is how to inhibit the NF-κB activity at optimal level. Thus, a modified E1A gene (E1AΔ) containing function domain (1—80 aa) and nuclear localization domain (139—243 aa) was used and cloned into an eucaryotic expression vector pcDNA3 to transfect the porcine aortic endothelial cells (PAEC). The stable transfectants were screened with G418. E1AΔ gene was able to be stably expressed in the PAEC and could not affect the growth of PAEC as analyzed by RT-PCR and cell growth rate. Reporter gene assay demonstrated that E1AΔ was capable of inhibiting NF-κB activity in the PAEC induced by TNF-α without sensitizing to apoptosis, and the rate of inhibition was 53%. Furthermore, E1 A Δ inhibited the expression of a NF-κB-dependent inflammatory gene E-selectin in the cells, and the rate of inhibition was 63%. In summary, the usage of E1AΔ gene may be a new strategy to overcome DXR in the xenotransplantation.
机译:转录因子核因子κB(NF-κB)在延迟异种移植排斥(DXR)中起关键作用。该领域的重要目的之一是如何以最佳水平抑制NF-κB活性。因此,使用包含功能域(1-80aa)和核定位域(139-243aa)的修饰的E1A基因(E1AΔ),并将其克隆到真核表达载体pcDNA3中,以转染猪主动脉内皮细胞(PAEC)。用G418筛选稳定的转染子。通过RT-PCR和细胞生长速率分析,E1AΔ基因能够在PAEC中稳定表达,并且不会影响PAEC的生长。 Reporter基因检测结果表明,E1AΔ能够抑制TNF-α诱导的PAEC中的NF-κB活性,而对细胞凋亡不敏感,抑制率为53%。此外,E1AΔ抑制细胞中NF-κB依赖性炎性基因E-选择素的表达,抑制率为63%。总之,E1AΔ基因的使用可能是克服异种移植中DXR的新策略。

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