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2000
Volume 5, Issue 4
  • ISSN: 1574-888X
  • E-ISSN: 2212-3946

Abstract

The discovery of several sources of hepatic progenitors in extra-hepatic organs and tissues, both in animal models and in humans, supports opportunities to isolate, grow and expand them in vitro. Microenvironment factors involved in regulating proliferation and commitment of liver cell precursors have been identified and better characterization of liver stem cell pathobiology would greatly improve the understanding of liver differentiation/ regeneration processes, especially those leading to hepatocarcinogenesis. The goal of these researches has been to discover the most available, suitable and easy-to-use pluripotent stem cells (PSC) sources for cell-based therapies in genetic and acquired liver diseases, therapies which to date have required liver transplantation, This report reviews the efforts, so far, to either investigate the presence of PSC in hepatic and extra-hepatic districts or evaluate their capacity to differentiate in vitro and to restore in vivo liver function.

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/content/journals/cscr/10.2174/157488810793351659
2010-12-01
2025-09-18
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/content/journals/cscr/10.2174/157488810793351659
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  • Article Type:
    Research Article
Keyword(s): adult stem cells; Asymmetric cell division; autologous transplantation; autoreplication activity; bile duct epithelium; biliary cells; binding protein; biomedical application; bipotent; bipotent precursors; blood-derived-cells; cell adhesion molecules; cell compartments; cell transplantation; Cirrhosis; clonogenic; developmental plasticity; diabetics; displastic lesions; ductular reactions; embryonic stem cells; epithelial cells; establishment factors; ex vivo; extra-hepatic origin; extrinsic and intrinsic stimuli; fibroblasts growth factor 4; gap junction formation; gene expression; hematopoietic cells; hematopoietic diseases reconstruction; hepatic cell lineage; hepatic markers albumin; Hepatic progenitor cells; hepatic progenitors cells; hepatoblasts; HUMAN HEPATOCYTE PROGENITORS; immune rejection; immune system; in vitro fertilized eggs; liver differentiation; liver milieu permits; liver mimics; liver morphologic; long-term maintenance; mammalian liver; mature hepatocyte of liver precursors; microenvironment; microenvironment influence; multi-factorial process; multiple organ-specific cell types; multipotent cells; murine embryonic; nuclear factor kappa B; nuclear reprogramming; nuclear reprogramming functions; optimal expandability of liver stem cells; organs; oval cells; plasticity; pluripotent cells; pluripotent stem cells; pluripotent stem-like cell population; proliferate; Purified HSC of murine; risk of transmitting infections; serum-free; specific mitogenic; Specific Selective-Cocktails; synergistic action; teratoma formation; trans-differentiation; Transcription Factors; Transplantation in animal; tumorogenic risk; umbilical cord
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