首页|靶向人c-Cbl基因重组干扰慢病毒与过表达腺病毒载体的构建、鉴定以及病毒功效研究

靶向人c-Cbl基因重组干扰慢病毒与过表达腺病毒载体的构建、鉴定以及病毒功效研究

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目的:构建可调控c-Cbl基因表达的重组慢病毒与腺病毒并评估其功效.方法:应用基因重组技术,分别构建靶向人c-Cbl基因的干扰慢病毒和过表达腺病毒.采用定量PCR和免疫印迹法检测病毒感染后白血病细胞(HL60、THP1)c-Cbl基因表达与转录本的变化.结果:3个靶向人c-Cbl基因的重组干扰慢病毒载体经测序验证构建成功,包装的病毒滴度均大于1 ×108 TU/ml,其中shRNA-2号慢病毒干扰效率最高,白血病细胞感染后c-Cbl基因的表达约下调95%,CBL蛋白的表达约下调60%;同时,靶向人c-Cbl基因的重组过表达腺病毒载体也经测序验证构建成功,包装的病毒滴度大于1 ×109 TU/ml,细胞感染腺病毒后,c-Cbl基因表达可瞬时上调约10倍,CBL蛋白表达约上调1.5倍.结论:重组干扰慢病毒和过表达腺病毒均可高效感染白血病细胞,并能分别下调和上调c-Cbl基因与CBL蛋白的表达,为后续研究肿瘤细胞内c-Cbl基因功能打下前期基础.
The Study of Recombinant Interfering Lentiviruses and Overex-pressed Adenovirus Vectors Targeting Human c-Cbl Gene:Con-struction,Identification and Efficacy
Objective:To construct recombinant lentivirus and adenovirus which regulate the expression of c-Cbl gene and evaluate their efficacy.Methods:The interference lentivirus and overexpressed adenovirus targeting human c-Cbl gene were constructed by gene recombination technology.Quantitative PCR and western blotting were used to detect the expression changes in c-Cbl gene and its transcription after leukemia cells(HL60,THP1)were infected by virus.Results:Three recombinant interfering lentiviral vectors targeting human c-Cbl genes to successfully constructed and were identified by DNA sequencing,and the titers of the packaged viruses were all greater than 1 x 108 TU/ml.Among them,shRNA-2 lentivirus had the highest interference efficiency,and the expression of c-Cbl gene and CBL protein were decreased about 95%and 60%respectively after leukemia cells were infected with shRNA-2;In addition,the recombinant overexpression adenovirus targeting human c-Cbl gene was packaged successfully with the virus titer greater than 1 x 109 TU/ml.When leukemia cells were infected with adenovirus,the expression of c-Cbl gene and CBL protein were up-regulated about 10 times and 1.5 times respectively.Conclusion:Both recombinant interfering lentivirus and overexpression adenovirus can efficiently infect leukemia cells and affect the expressions of c-Cbl gene and CBL protein.It will lay a preliminary foundation for the subsequent study on the function of c-Cbl gene in tumor cells.

c-Cbl genelentivirus vectotadenovirus vector

孙启鑫、吴秉毅、姚倩倩、黄志伟、朱志刚

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广州市第一人民医院(华南理工大学第二附属医院)老年血液肿瘤科,广东广州 510180

中山大学肿瘤研究中心血液肿瘤科,广东广州 510060

南方医科大学珠江医院血液科,广东广州 510260

c-Cbl基因 慢病毒载体 腺病毒载体

广东省医学科研项目广东省高水平大学建设项目广州市医学重点学科建设项目

A2019508LC2016ZD026ZDXK202103

2024

中国实验血液学杂志
中国病理生理学会

中国实验血液学杂志

CSTPCD北大核心
影响因子:0.988
ISSN:1009-2137
年,卷(期):2024.32(1)
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