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Persistent hepatitis C virus infection in microscale primary human hepatocyte cultures

机译:微型原代人肝细胞培养物中的持久性丙型肝炎病毒感染

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摘要

Hepatitis C virus (HCV) remains a major public health problem, affecting approximately 130 million people worldwide. HCV infection can lead to cirrhosis, hepatocellular carcinoma, and end-stage liver disease, as well as extrahepatic complications such as cryoglobulinemia and lymphoma. Preventative and therapeutic options are severely limited; there is no HCV vaccine available, and nonspecific, IFN-based treatments are frequently ineffective. Development of targeted antivirals has been hampered by the lack of robust HCV cell culture systems that reliably predict human responses. Here, we show the entire HCV life cycle recapitulated in micropatterned cocultures (MPCCs) of primary human hepatocytes and supportive stroma in a multiwell format. MPCCs form polarized cell layers expressing all known HCV entry factors and sustain viral replication for several weeks. When coupled with highly sensitive fluorescence- and luminescence-based reporter systems, MPCCs have potential as a high-throughput platform for simultaneous assessment of in vitro efficacy and toxicity profiles of anti-HCV therapeutics.
机译:丙型肝炎病毒(HCV)仍然是一个主要的公共健康问题,全球约有1.3亿人受到影响。 HCV感染可导致肝硬化,肝细胞癌和终末期肝病,以及肝外并发症,例如冷球蛋白血症和淋巴瘤。预防和治疗选择受到严格限制;没有可用的HCV疫苗,而且基于IFN的非特异性治疗通常无效。缺乏可靠地预测人类反应的健壮HCV细胞培养系统,阻碍了靶向抗病毒药的开发。在这里,我们以多孔形式展示了原代人肝细胞和支持性基质的微模式共培养(MPCC)中概括的整个HCV生命周期。 MPCC形成表达所有已知HCV进入因子的极化细胞层,并维持病毒复制数周。与高度敏感的基于荧光和发光的报告系统结合使用时,MPCC具有作为高通量平台的潜力,可同时评估抗HCV治疗剂的体外功效和毒性。

著录项

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  • 作者单位

    Center for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065;

    rnDivision of Health Sciences and Technology, Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02139;

    rnCenter for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065;

    rnCenter for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065;

    rnDivision of Health Sciences and Technology, Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02139;

    rnCenter for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065;

    rnCenter for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065;

    rnCenter for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065;

    rnCenter for the Study of Hepatitis C, The Rockefeller University, New York, NY 10065 Laboratory of Virology and Infectious Diseases, The Rockefeller University, New York, NY 10065 Division of Health Sciences and Technology, Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA 02139;

    Howard Hughes Medical Institute, Cambridge, MA 02139 Division of Medicine, Brigham and Women's Hospital, Boston, MA 02115;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    viral hepatitis; liver; tissue engineering; drug development; infection;

    机译:病毒性肝炎;肝;组织工程;药物开发;感染;
  • 入库时间 2022-08-18 00:41:13

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