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[含米非司酮(RU486)诱导型NRF2基因调控系统的腺病毒体外构建与鉴定]

[In vitro construction and confirmation of adenovirus containing a mifepristone (RU486)-inducible regulation system for NRF2 gene].

作者信息

Cai Qi-qi, Hong Guang-liang, Qiu Qiao-meng, Li Lin-fang, Lu Zhong-qiu, Wu Hong-ping, Wang Duan-ming, Liang Huan

机构信息

Emergency Medical Department, First Affiliated Hospital, Wenzhou Medical College, Wenzhou 325000, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2011 Jan 18;91(3):198-202.

Abstract

OBJECTIVE

To construct an adenovirus containing a mifepristone (RU486)-inducible regulation system for NRF2 gene, express the product in H460 cell and verify whether the mentioned system can control the gene expression and assess its efficiency.

METHODS

A RU486-inducible regulation system for Nrf2 gene was introduced into an adenovirus. The confirmation was performed through the LUC and Dsred genes. And the expression pattern of Nrf2 at the viral level was examined by Western blot and RT-PCR (reverse transcription-polymerase chain reaction).

RESULTS

The expressions of LUC and Dsred showed a rising trend with the incremental dose of RU486. After the transfection H460 cell with Ad-RUNrf2, the results of RT-PCR and Western blot demonstrated that the expression of Nrf2 was elevated with a rising dose of RU486. After the removal of RU486, the expression of Nrf2 was reduced.

CONCLUSION

The construction of an adenovirus carrying Nrf2 gene regulated by a RU486-inducible system is successful, and RU486 can adjust the cellular expression of Nrf2 factor. The LUC and the Dsred expression assumes the dosage dependence along with RU486 to increase; after the Ad-RUNrf2 infects the H460 cell, through RTPCR and Western the Blot result demonstrated that the expression of Nrf2 increases along with the RU486 dosage increases, after removing RU486, the Nrf2 expression is weaken. Showing the construction of the adenovirus carrying Nrf2 gene regulated by the mifepristone (RU486)-inducible system is successful, and RU486 can adjust the Nrf2 factor in the cell the expression.

摘要

目的

构建含米非司酮(RU486)诱导调控系统的NRF2基因腺病毒,在H460细胞中表达产物,验证该系统能否调控基因表达并评估其效率。

方法

将Nrf2基因的RU486诱导调控系统导入腺病毒。通过LUC和Dsred基因进行确认。通过蛋白质免疫印迹法和逆转录-聚合酶链反应(RT-PCR)检测病毒水平Nrf2的表达模式。

结果

随着RU486剂量增加,LUC和Dsred的表达呈上升趋势。用Ad-RUNrf2转染H460细胞后,RT-PCR和蛋白质免疫印迹法结果表明,随着RU486剂量增加,Nrf2的表达升高。去除RU486后,Nrf2的表达降低。

结论

构建由RU486诱导系统调控的携带Nrf2基因的腺病毒成功,且RU486可调节细胞中Nrf2因子的表达。LUC和Dsred的表达随RU486增加呈剂量依赖性;Ad-RUNrf2感染H460细胞后,通过RT-PCR和蛋白质免疫印迹法结果表明,Nrf2的表达随RU486剂量增加而增加,去除RU486后,Nrf2表达减弱。表明构建由米非司酮(RU486)诱导系统调控的携带Nrf2基因的腺病毒成功,且RU486可调节细胞中Nrf2因子的表达。

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