Literature DB >> 8883463

Pluripotential liver stem cells: facultative stem cells located in the biliary tree.

M R Alison1, M H Golding, C E Sarraf.   

Abstract

The ability of the liver to regenerate after parenchymal damage is usually accomplished by the ephemeral entry of normally proliferatively quiescent (G0) hepatocytes into the cell cycle. However, when hepatocyte regeneration is defective, arborizing ductules which are continuous with the biliary tree, proliferate and migrate into the surrounding parenchyma. In man these biliary cells have variously been referred to as ductular structures, neoductules and neocholangioles, and have been observed in many forms of chronic liver disease, including cancer. In experimental animals similar ductal cells are usually called oval cells, and their association with defective regeneration has led to the belief that these cells represent a progenitor cell population. Oval cells are thought to take over the burden of regenerative growth after substantial hepatocyte loss, suggesting that they are the progeny of facultative stem cells. The liver is not, however, generally considered as a stem cell-fed hierarchy, although this is disputed by others. Despite this, the subject of oval cells has aroused intense interest as these cells may represent a target population for hepatic carcinogens, and they may be useful vehicles for ex vivo gene therapy. This review proposes that the liver does harbour stem cells which are located throughout the biliary epithelium, and that oval cells represent the progeny of these stem cells and function as an amplification compartment for the generation of 'new' hepatocytes. This is a conditional process which only occurs when the regenerative capacity of hepatocytes is overwhelmed and thus, unlike the intestinal epithelium, the liver is not behaving as a classical continually renewing stem cell-fed lineage. We focus on the biliary network, not merely as a conduit for bile, but also as a cell compartment with the potential to proliferate under appropriate conditions and give rise to fully differentiated hepatocytes and other cell types.

Entities:  

Mesh:

Year:  1996        PMID: 8883463     DOI: 10.1111/j.1365-2184.1996.tb00982.x

Source DB:  PubMed          Journal:  Cell Prolif        ISSN: 0960-7722            Impact factor:   6.831


  21 in total

Review 1.  The new stem cell biology: something for everyone.

Authors:  S L Preston; M R Alison; S J Forbes; N C Direkze; R Poulsom; N A Wright
Journal:  Mol Pathol       Date:  2003-04

Review 2.  Hepatic stem cells: from inside and outside the liver?

Authors:  M R Alison; P Vig; F Russo; B W Bigger; E Amofah; M Themis; S Forbes
Journal:  Cell Prolif       Date:  2004-02       Impact factor: 6.831

3.  Biliary tree stem/progenitor cells in glands of extrahepatic and intraheptic bile ducts: an anatomical in situ study yielding evidence of maturational lineages.

Authors:  Guido Carpino; Vincenzo Cardinale; Paolo Onori; Antonio Franchitto; Pasquale Bartolomeo Berloco; Massimo Rossi; Yunfang Wang; Rossella Semeraro; Maurizio Anceschi; Roberto Brunelli; Domenico Alvaro; Lola M Reid; Eugenio Gaudio
Journal:  J Anat       Date:  2011-12-05       Impact factor: 2.610

4.  Stem cell technology. Interview by Abi Berger.

Authors:  P A Fontes; A W Thomson
Journal:  BMJ       Date:  1999-11-13

Review 5.  Liver repopulation for the treatment of metabolic diseases.

Authors:  M Grompe
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

6.  Origin and structural evolution of the early proliferating oval cells in rat liver.

Authors:  S Paku; J Schnur; P Nagy; S S Thorgeirsson
Journal:  Am J Pathol       Date:  2001-04       Impact factor: 4.307

Review 7.  The fetal liver as cell source for the regenerative medicine of liver and pancreas.

Authors:  Rossella Semeraro; Vincenzo Cardinale; Guido Carpino; Raffaele Gentile; Cristina Napoli; Rosanna Venere; Manuela Gatto; Roberto Brunelli; Eugenio Gaudio; Domenico Alvaro
Journal:  Ann Transl Med       Date:  2013-07

Review 8.  Recent advances in the morphological and functional heterogeneity of the biliary epithelium.

Authors:  Yuyan Han; Shannon Glaser; Fanyin Meng; Heather Francis; Marco Marzioni; Kelly McDaniel; Domenico Alvaro; Julie Venter; Guido Carpino; Paolo Onori; Eugenio Gaudio; Gianfranco Alpini; Antonio Franchitto
Journal:  Exp Biol Med (Maywood)       Date:  2013-05

9.  FGF7 is a functional niche signal required for stimulation of adult liver progenitor cells that support liver regeneration.

Authors:  Hinako M Takase; Tohru Itoh; Seitaro Ino; Ting Wang; Takehiko Koji; Shizuo Akira; Yasuhiro Takikawa; Atsushi Miyajima
Journal:  Genes Dev       Date:  2013-01-15       Impact factor: 11.361

10.  Specific fate decisions in adult hepatic progenitor cells driven by MET and EGFR signaling.

Authors:  Mitsuteru Kitade; Valentina M Factor; Jesper B Andersen; Akira Tomokuni; Kosuke Kaji; Hirofumi Akita; Agnes Holczbauer; Daekwan Seo; Jens U Marquardt; Elizabeth A Conner; Seung-Bum Lee; Yun-Han Lee; Snorri S Thorgeirsson
Journal:  Genes Dev       Date:  2013-08-01       Impact factor: 11.361

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.