首页> 美国卫生研究院文献>Journal of Virology >Jaagsiekte Sheep Retrovirus and Enzootic Nasal Tumor Virus Promoters Drive Gene Expression in All Airway Epithelial Cells of Mice but Only Induce Tumors in the Alveolar Region of the Lungs
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Jaagsiekte Sheep Retrovirus and Enzootic Nasal Tumor Virus Promoters Drive Gene Expression in All Airway Epithelial Cells of Mice but Only Induce Tumors in the Alveolar Region of the Lungs

机译:Jaagsiekte绵羊逆转录病毒和鼻腔鼻肿瘤病毒启动子驱动小鼠所有气道上皮细胞中的基因表达但仅在肺泡区域诱导肿瘤。

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摘要

Jaagsiekte sheep retrovirus (JSRV) induces tumors in the distal airways of sheep and goats, while the closely related enzootic nasal tumor virus type 1 (ENTV-1) and ENTV-2 induce tumors in the nasal epithelium of sheep and goats, respectively. When expressed using a strong Rous sarcoma virus promoter, the envelope proteins of these viruses induce tumors in the respiratory tract of mice, but only in the distal airway. To examine the role of the retroviral long terminal repeat (LTR) promoters in determining tissue tropism, adeno-associated virus (AAV) vectors expressing alkaline phosphatase under the control of the JSRV, ENTV-1, or ENTV-2 LTRs were generated and administered to mice. The JSRV LTR was active in all airway epithelial cells, while the ENTV LTRs were active in the nasal epithelium and alveolar type II cells but poorly active in tracheal and bronchial epithelial cells. When vectors were administered systemically, the ENTV-1 and -2 LTRs were inactive in major organs examined, whereas the JSRV showed high-level activity in the liver. When a putative transcriptional enhancer from the 3′ end of the env gene was inserted upstream of the JSRV and ENTV-1 LTRs in the AAV vectors, a dramatic increase in transgene expression was observed. However, intranasal administration of AAV vectors containing any combination of ENTV or JSRV LTRs and Env proteins induced tumors only in the lower airway. Our results indicate that mice do not provide an adequate model for nasal tumor induction by ENTV despite our ability to express genes in the nasal epithelium.
机译:Jaagsiekte绵羊逆转录病毒(JSRV)在绵羊和山羊的远端气道中诱发肿瘤,而密切相关的1型鼻病毒性鼻肿瘤病毒(ENTV-1)和ENTV-2在绵羊和山羊的鼻上皮中分别诱发肿瘤。当使用强大的劳斯肉瘤病毒启动子表达时,这些病毒的包膜蛋白在小鼠的呼吸道中诱导肿瘤,但仅在远端呼吸道中诱导肿瘤。为了检查逆转录病毒长末端重复序列(LTR)启动子在确定组织嗜性中的作用,生成并施用了在JSRV,ENTV-1或ENTV-2 LTRs的控制下表达碱性磷酸酶的腺相关病毒(AAV)载体。给老鼠。 JSRV LTR在所有气道上皮细胞中均具有活性,而ENTV LTR在鼻上皮细胞和II型肺泡细胞中具有活性,但在气管和支气管上皮细胞中的活性较弱。当系统地施用载体时,在所检查的主要器官中ENTV-1和-2 LTR不活跃,而JSRV在肝脏中显示出高水平的活性。当将来自env基因3'端的假定转录增强子插入AAV载体中JSRV和ENTV-1 LTR的上游时,观察到转基因表达显着增加。但是,鼻内施用含有ENTV或JSRV LTR和Env蛋白的任何组合的AAV载体只能在下呼吸道诱导肿瘤。我们的结果表明,尽管我们能够在鼻上皮细胞中表达基因,但小鼠并未提供ENTV诱导鼻肿瘤的适当模型。

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