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本文引用的文献

1
Brief report: phenotypic rescue of induced pluripotent stem cell-derived motoneurons of a spinal muscular atrophy patient.简要报告:脊髓性肌萎缩症患者诱导多能干细胞衍生运动神经元的表型挽救。
Stem Cells. 2011 Dec;29(12):2090-3. doi: 10.1002/stem.749.
2
Design, synthesis, and biological evaluation of triazolo-pyrimidine derivatives as novel inhibitors of hepatitis B virus surface antigen (HBsAg) secretion.设计、合成及三唑嘧啶衍生物作为新型乙型肝炎病毒表面抗原(HBsAg)分泌抑制剂的生物评价。
J Med Chem. 2011 Aug 25;54(16):5660-70. doi: 10.1021/jm200696v. Epub 2011 Aug 2.
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Understanding the host genetics of chronic hepatitis B and C.理解慢性乙型肝炎和丙型肝炎的宿主遗传学。
Semin Liver Dis. 2011 May;31(2):115-27. doi: 10.1055/s-0031-1276642. Epub 2011 May 2.
4
Hepatitis B virus limits response of human hepatocytes to interferon-α in chimeric mice.乙型肝炎病毒限制嵌合小鼠人肝细胞对干扰素-α的反应。
Gastroenterology. 2011 Jun;140(7):2074-83, 2083.e1-2. doi: 10.1053/j.gastro.2011.02.057. Epub 2011 Mar 2.
5
A humanized mouse model to study hepatitis C virus infection, immune response, and liver disease.用于研究丙型肝炎病毒感染、免疫反应和肝病的人源化小鼠模型。
Gastroenterology. 2011 Apr;140(4):1334-44. doi: 10.1053/j.gastro.2011.01.001. Epub 2011 Jan 13.
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A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.利用人类诱导多能干细胞进行神经发育和雷特综合征治疗的模型。
Cell. 2010 Nov 12;143(4):527-39. doi: 10.1016/j.cell.2010.10.016.
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Pluripotency and cellular reprogramming: facts, hypotheses, unresolved issues.多能性与细胞重编程:事实、假说、未解问题。
Cell. 2010 Nov 12;143(4):508-25. doi: 10.1016/j.cell.2010.10.008.
8
Characterization of Human Huntington's Disease Cell Model from Induced Pluripotent Stem Cells.源自诱导多能干细胞的人类亨廷顿舞蹈病细胞模型的特性分析
PLoS Curr. 2010 Oct 28;2:RRN1193. doi: 10.1371/currents.RRN1193.
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Modeling inherited metabolic disorders of the liver using human induced pluripotent stem cells.使用人诱导多能干细胞建立肝脏遗传代谢性疾病模型。
J Clin Invest. 2010 Sep;120(9):3127-36. doi: 10.1172/JCI43122. Epub 2010 Aug 25.
10
Human motor neuron generation from embryonic stem cells and induced pluripotent stem cells.人胚胎干细胞和诱导多能干细胞生成运动神经元。
Cell Mol Life Sci. 2010 Nov;67(22):3837-47. doi: 10.1007/s00018-010-0463-y. Epub 2010 Jul 29.

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.

DOI:10.1007/s12272-012-0206-8
PMID:22370780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3731984/
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。