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利用人诱导多能干细胞建立乙型肝炎病毒和丙型肝炎病毒的人源化小鼠模型。

Humanized murine model for HBV and HCV using human induced pluripotent stem cells.

机构信息

Department of Genetics, Yale Stem Cell Center, Yale School of Medicine, New Haven, CT 06520, USA.

出版信息

Arch Pharm Res. 2012 Feb;35(2):261-9. doi: 10.1007/s12272-012-0206-8. Epub 2012 Feb 28.

Abstract

Infection of hepatitis B virus (HBV) and hepatitis C virus (HCV) results in heterogeneous outcomes from acute asymptomatic infection to chronic infection leading to cirrhosis and hepatocellular carcinoma (HCC). In vitro models using animal hepatocytes, human HCC cell lines, or in vivo transgenic mouse models have contributed invaluably to understanding the pathogenesis of HBV and HCV. A humanized mouse model made by reconstitution of human primary hepatocytes in the liver of the immunodeficient mouse provides a novel experimental opportunity which mimics the in vivo growth of the human hepatocytes. The limited access to primary human hepatocytes necessitated the search for other cellular sources, such as pluripotent stem cells. Human embryonic stem cells (hESCs) have the features of self-renewal and pluripotency and differentiate into cells of all three germ layers, including hepatocytes. Humaninduced pluripotent stem cells (iPSCs) derived from the patient's or individual's own cells provide a novel opportunity to generate hepatocyte-like cells with the defined genetic composition. Here, we will review the current perspective of the models used for HBV and HCV study, and introduce the personalized mouse model using human iPSCs. This novel mouse model will facilitate the direct investigation of HBV and HCV in human hepatocytes as well as probing the genetic influence on the susceptibility of hepatocytes to HBV and HCV.

摘要

乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)的感染可导致从急性无症状感染到慢性感染的不同结局,进而导致肝硬化和肝细胞癌(HCC)。使用动物肝细胞、人 HCC 细胞系或体内转基因小鼠模型的体外模型为理解 HBV 和 HCV 的发病机制做出了宝贵的贡献。用人原发性肝细胞在免疫缺陷小鼠的肝脏中重建而制成的人源化小鼠模型提供了一种新的实验机会,可以模拟人肝细胞的体内生长。由于原发性人肝细胞的获取有限,因此需要寻找其他细胞来源,例如多能干细胞。人胚胎干细胞(hESCs)具有自我更新和多能性的特点,并分化为包括肝细胞在内的三个胚层的细胞。源自患者或个体自身细胞的人诱导多能干细胞(iPSCs)为生成具有明确遗传组成的肝细胞样细胞提供了新的机会。在这里,我们将回顾用于 HBV 和 HCV 研究的模型的最新观点,并介绍使用人 iPSCs 的个性化小鼠模型。这种新型小鼠模型将有助于直接研究 HBV 和 HCV 在人肝细胞中的作用,并探究遗传因素对肝细胞易感染 HBV 和 HCV 的影响。

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