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[在Sf9昆虫细胞中包装的重组腺相关病毒6型的随机整合分析]

[Random Integration Analysis of Recombinant Adeno-Associated Virus 6 Packaged in Sf9 Insect Cells].

作者信息

Zhang M H, Liu X M, Zhang C

机构信息

School of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230026 China.

Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, 215163 China.

出版信息

Mol Biol (Mosk). 2023 Jul-Aug;57(4):709-712.

Abstract

Recently, there have been growing concerns over the integration of recombinant adeno-associated virus (rAAV) used in gene therapy. Wild-type adeno-associated virus (AAV) site specifically integrates into AAVS1 site of human genome, while rAAV randomly integrates into host chromosomes at low frequencies. This research aims to study the random integration events of rAAV6-EGFP packaged in Sf9 insect cells. Baculo-Sf9 manufacturing platform has the advantages of high-density suspension culture of Sf9 insect cells and large-scale production of rAAV vectors. In this study, we used different doses of Baculo-Sf9 produced rAAV6-EGFP to transduce HEK293T cells and A549-implanted tumors in vitro and in vivo. Using flow cytometry and fluorescence microscopy, we studied their EGFP gene expression efficiencies and EGFP fluorescence intensities. Using inverse nested PCR and DNA sequencing, random integration sites of rAAV6-EGFP genome into human chromosomes were identified. In vitro results showed that gene expression efficiencies became stable after 20 days and random integration frequencies were 0.2-4.2%. Both in vitro and in vivo results indicated that random integration of Baculo-Sf9 rAAV6 was dose-dependent. Sequencing results showed two random integration sites, which were on human chromosomes 8 and 12. The findings suggest that we should use as low dose of rAAV vector as possible for safe gene therapy.

摘要

最近,人们对基因治疗中使用的重组腺相关病毒(rAAV)的整合问题越来越关注。野生型腺相关病毒(AAV)会特异性地整合到人类基因组的AAVS1位点,而rAAV则以低频率随机整合到宿主染色体中。本研究旨在探讨在Sf9昆虫细胞中包装的rAAV6-EGFP的随机整合事件。杆状病毒-Sf9生产平台具有Sf9昆虫细胞高密度悬浮培养和大规模生产rAAV载体的优势。在本研究中,我们使用不同剂量的杆状病毒-Sf9生产的rAAV6-EGFP在体外和体内转导HEK293T细胞和植入A549细胞的肿瘤。通过流式细胞术和荧光显微镜,我们研究了它们的EGFP基因表达效率和EGFP荧光强度。使用反向巢式PCR和DNA测序,鉴定了rAAV6-EGFP基因组在人类染色体上的随机整合位点。体外结果显示,20天后基因表达效率变得稳定,随机整合频率为0.2-4.2%。体外和体内结果均表明,杆状病毒-Sf9 rAAV6的随机整合具有剂量依赖性。测序结果显示了两个随机整合位点,分别位于人类染色体8和12上。这些发现表明,为了安全的基因治疗,我们应尽可能使用低剂量的rAAV载体。

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