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表达全长丙型肝炎病毒cDNA的转基因小鼠。

Transgenic mouse expressing a full-length hepatitis C virus cDNA.

作者信息

Matsuda J, Suzuki M, Nozaki C, Shinya N, Tashiro K, Mizuno K, Uchinuno Y, Yamamura K

机构信息

The Chemo-Sero-Therapeutic Research Institute, Kikuchi Research Center, Pathology Department, Kumamoto.

出版信息

Jpn J Cancer Res. 1998 Feb;89(2):150-8. doi: 10.1111/j.1349-7006.1998.tb00543.x.

Abstract

Hepatitis C virus (HCV), a major causative agent of post transfusion non-A, non-B hepatitis (NANBH), can only infect humans and chimpanzees. We produced nine transgenic mouse lines carrying a full-length HCV cDNA with the human serum amyloid P component (hSAP) promoter that can direct liver-specific expression. In one of these lines HCV mRNA and HCV core protein were detected in the liver of the transgenic mouse, although the levels of expression were very low. In addition, HCV-related antibody was detected in the serum.

摘要

丙型肝炎病毒(HCV)是输血后非甲非乙型肝炎(NANBH)的主要致病因子,仅感染人类和黑猩猩。我们构建了九条携带全长HCV cDNA并由人血清淀粉样蛋白P成分(hSAP)启动子驱动的转基因小鼠品系,该启动子可指导肝脏特异性表达。在其中一个品系的转基因小鼠肝脏中检测到了HCV mRNA和HCV核心蛋白,尽管表达水平很低。此外,在血清中检测到了HCV相关抗体。

相似文献

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Transgenic mouse expressing a full-length hepatitis C virus cDNA.表达全长丙型肝炎病毒cDNA的转基因小鼠。
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本文引用的文献

6
Hepatitis C virus core and E2 protein expression in transgenic mice.
Hepatology. 1997 Mar;25(3):719-27. doi: 10.1002/hep.510250338.
8
Genetic analysis of the hepatitis C virus (HCV) genome from HCV-infected human T cells.
J Gen Virol. 1997 Feb;78 ( Pt 2):329-36. doi: 10.1099/0022-1317-78-2-329.

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