Bertran J, Miller J L, Yang Y, Fenimore-Justman A, Rueda F, Vanin E F, Nienhuis A W
Department of Hematology/Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
J Virol. 1996 Oct;70(10):6759-66. doi: 10.1128/JVI.70.10.6759-6766.1996.
Adeno-associated virus has a broad host range, is nonpathogenic, and integrates into a preferred location on chromosome 19, features that have fostered development of recombinant adeno-associated viruses (rAAV) as gene transfer vectors for therapeutic applications. We have used an rAAV to transfer and express the murine cationic amino acid transporter which functions as the ecotropic retroviral receptor, thereby rendering human cells conditionally susceptible to infection by an ecotropic retroviral vector. The proportion of human HeLa cells expressing the receptor at 60 h varied as a function of the multiplicity of infection (MOI) with the rAAV. Cells expressing the ecotropic receptor were efficiently transduced with an ecotropic retroviral vector encoding a nucleus-localized form of beta-galactosidase. Cells coexpressing the ecotropic receptor and nucleus-localized beta-galactosidase were isolated by fluorescence-activated cell sorting, and cell lines were recovered by cloning at limiting dilution. After growth in culture, all clones contained the retroviral vector genome, but fewer than 10% (3 of 47) contained the rAAV genome and continued to express the ecotropic receptor. The ecotropic receptor coding sequences in the rAAV genome were under the control of a tetracycline-modulated promoter. In the presence of tetracycline, receptor expression was low and the proportion of cells transduced by the ecotropic retroviral vector was decreased. Modulation of receptor expression was achieved with both an episomal and an integrated form of the rAAV genome. These data establish that functional gene expression from an rAAV genome can occur transiently without genome integration.
腺相关病毒具有广泛的宿主范围,无致病性,并整合到19号染色体上的一个优选位置,这些特性促进了重组腺相关病毒(rAAV)作为治疗应用的基因转移载体的发展。我们已使用rAAV来转移和表达鼠阳离子氨基酸转运体,该转运体作为嗜亲性逆转录病毒受体发挥作用,从而使人细胞有条件地易受嗜亲性逆转录病毒载体的感染。在60小时时表达该受体的人HeLa细胞比例随rAAV感染复数(MOI)而变化。用编码细胞核定位形式的β-半乳糖苷酶的嗜亲性逆转录病毒载体有效地转导表达嗜亲性受体的细胞。通过荧光激活细胞分选分离共表达嗜亲性受体和细胞核定位的β-半乳糖苷酶的细胞,并通过有限稀释克隆回收细胞系。在培养中生长后,所有克隆都含有逆转录病毒载体基因组,但少于10%(47个中的3个)含有rAAV基因组并继续表达嗜亲性受体。rAAV基因组中的嗜亲性受体编码序列受四环素调节启动子的控制。在四环素存在下,受体表达低,嗜亲性逆转录病毒载体转导的细胞比例降低。rAAV基因组的附加型和整合型均可实现受体表达的调节。这些数据表明,rAAV基因组的功能性基因表达可在不进行基因组整合的情况下短暂发生。