In vitro differentiation of mouse ES cells into hepatocytes with coagulation factors VIII and IX expression profiles
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  • 作者:Ying Meng (1)
    Shaoliang Huang (1) (2)
    Jun Min (1) (3)
    Zhongmin Guo (4)
  • 关键词:ES cell ; differentiation ; hepatocyte ; coagulation factor
  • 刊名:Science China Life Sciences
  • 出版年:2006
  • 出版时间:June 2006
  • 年:2006
  • 卷:49
  • 期:3
  • 页码:259-264
  • 全文大小:9120KB
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  • 作者单位:Ying Meng (1)
    Shaoliang Huang (1) (2)
    Jun Min (1) (3)
    Zhongmin Guo (4)

    1. Center for Stem Cell Research, the Second Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510120, China
    2. Department of Pediatrics, the Second Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510120, China
    3. Department of Surgery, the Second Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510120, China
    4. Experimental Animal Center, Sun Yat-sen Medical College, Sun Yat-sen University, Guangzhou, 510089, China
文摘
Coagulation factors II, V, VII, VIII, IX and X are produced by hepatocytes. So factors VIII and IX deficiencies, which result in hemophilia A and B, have the potential to respond to cellular replacement therapy. Embryonic stem (ES) cells provide a unique source for therapeutic applications. Here, E14 mouse ES cells have been induced into hepatocytes in vitro. Morphology revealed that ES-derived hepatic-like cells were round or polyhedral shaped with distinct boundary of individual cells, and some arranged in trabeculae. These cells expressed endodermal-or liver-specific mRNA—transthyretin (TTR), α1-anti-trypsin (AAT), α-fetoprotein (AFP), albumin (ALB), glucose-6-phoshpatase (G6P) and tyrosine aminotransferase (TAT). Approximately (85.1±0.5)% of the ES-derived cells was stained positive green with ICG uptake. These cells were also stained magenta as a result of PAS reaction. In this paper, expression of coagulation factors VIII and IX mRNA in the ES-derived cells is documented. Therefore, ES cells might be developed as substitute donor cells for the therapy of coagulation factor deficiencies.

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