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通过流体动力学转染构建的小鼠模型中乙型肝炎病毒产生的超微结构证明

Ultrastructural demonstration of hepatitis B virus production in a mouse model produced by hydrodynamic transfection.

作者信息

Konishi Masayoshi, Tanaka Hideaki, Kaito Masahiko, Fujita Naoki, Iwasa Motoh, Kobayashi Yoshinao, Adachi Yukihiko, Watanabe Shozo

机构信息

Center for Physical and Mental Health, Mie University, Mie, Japan.

出版信息

Int J Mol Med. 2007 Jul;20(1):31-6.

Abstract

A mouse model of hepatitis B virus (HBV) infection produced by hydrodynamic injection of HBV DNA has been recently established. However, the ultrastructural demonstration of HBV particles in this mouse model has not as yet been reported. In our study, plasmid DNA containing wild-type HBV DNA was rapidly injected into 8-week-old female SCID mice via the tail vein. Serum levels of HBsAg were measured by ELISA kit. Intrahepatic HBV protein expression was detected by immunohistochemistry of HBcAg. Ultrastructural study of the serum samples was performed by transmission electron microscopy and immunogold electron microscopy. Serum HBsAg and intrahepatic HBcAg were detected in HBV DNA-injected mice for at least 14 days. Spherical and filamentous particles 22 nm in diameter and double-shelled Dane-like particles 42 nm in diameter were detected in the sera of mice. The ultrastructural features of these particles were identical to HBV particles observed in serum from chronic hepatitis B patients. These particles were confirmed to be HBV particles by immunogold electron microscopy. We conclude that our present HBV mouse model using hydrodynamic transfection of HBV DNA is appropriate for production of HBV virions including Dane particles. This mouse model may be useful for screening in vivo the efficacy of antiviral drugs.

摘要

最近通过水动力注射乙肝病毒(HBV)DNA建立了一种HBV感染的小鼠模型。然而,尚未有关于此小鼠模型中HBV颗粒超微结构的报道。在我们的研究中,将含有野生型HBV DNA的质粒DNA经尾静脉快速注射到8周龄雌性SCID小鼠体内。用ELISA试剂盒检测血清中HBsAg水平。通过HBcAg免疫组化检测肝内HBV蛋白表达。通过透射电子显微镜和免疫金电子显微镜对血清样本进行超微结构研究。在注射HBV DNA的小鼠中至少14天检测到血清HBsAg和肝内HBcAg。在小鼠血清中检测到直径22 nm的球形和丝状颗粒以及直径42 nm的双壳样 Dane颗粒。这些颗粒的超微结构特征与慢性乙型肝炎患者血清中观察到的HBV颗粒相同。通过免疫金电子显微镜证实这些颗粒为HBV颗粒。我们得出结论,我们目前使用HBV DNA水动力转染的HBV小鼠模型适合产生包括 Dane颗粒在内的HBV病毒体。该小鼠模型可能有助于体内筛选抗病毒药物的疗效。

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