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Genetic heterogeneity in response to adenovirus gene therapy

机译:腺病毒基因治疗的遗传异质性

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Background After intravenous delivery of the adenoviral vector into rats or mice, 95–99% of the encoded protein is produced in the hepatocytes. We observed, as have others, that the early expression levels of the vector encoded protein vary, greatly, within a species, from one animal strain to another. This study was initiated to determine the molecular mechanism causing the difference: hepatic transfection, transcription or translation. For this purpose different doses of Ad5 luciferase and Ad5 LacZ were intravenously injected into Brown Norway rats and Wag/Rij rats, two strains that differ by a factor of 10 in encoded protein levels. The proportion of LacZ positive hepatocytes, the adenoviral DNA, specific transgenic RNA and luciferase protein were compared in the two strains. Results The number of transduced hepatocytes and the amounts of Ad5 DNA in the livers was similar in both strains, whereas the Brown Norway rats produced 8 to 10 times more of both vector encoded proteins and of transgene mRNA than the Wag/Rij rats. Conclusions It is concluded that the difference between strains in vector encoded protein expression is due to different transcriptional events. No evidence was obtained to suggest that the differences are related to liver damage influenced by vector toxicity or immune reactions.
机译:背景技术在将腺病毒载体静脉内递送至大鼠或小鼠后,肝细胞中产生了95–99%的编码蛋白。与其他动物一样,我们观察到,载体编码的蛋白质的早期表达水平在一个物种内,从一个动物品系到另一个动物品系,变化很大。开始这项研究以确定引起这种差异的分子机制:肝转染,转录或翻译。为此,将不同剂量的Ad5荧光素酶和Ad5 LacZ静脉注射到Brown Norway大鼠和Wag / Rij大鼠中,这两种菌株的编码蛋白水平相差10倍。比较了两个菌株中LacZ阳性肝细胞,腺病毒DNA,特异性转基因RNA和荧光素酶蛋白的比例。结果两种菌株中肝细胞的转导肝细胞数目和Ad5 DNA量相似,而褐挪威大鼠产生的载体编码蛋白和转基因mRNA均比Wag / Rij大鼠高8至10倍。结论结论是,菌株之间载体编码的蛋白表达的差异是由于不同的转录事件所致。没有证据表明差异与载体毒性或免疫反应影响肝脏损害有关。

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