Wound healing in the liver with particular reference to stem cells
- PMID: 9684285
- PMCID: PMC1692283
- DOI: 10.1098/rstb.1998.0252
Wound healing in the liver with particular reference to stem cells
Abstract
The efficiency of liver regeneration in response to the loss of hepatocytes is widely acknowledged, and this is usually accomplished by the triggering of normally proliferatively quiescent hepatocytes into the cell cycle. However, when regeneration is defective, tortuous ductular structures, initially continuous with the biliary tree, proliferate and migrate into the surrounding hepatocyte parenchyma. In humans, 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 impaired regeneration has led to the conclusion that they are the progeny of facultative stem cells. Oval cells are of considerable biological interest as they may represent a target population for hepatic carcinogens, and they may also be useful vehicles for ex vivo gene therapy for the correction of inborn errors of metabolism. This review proposes that the liver harbours stem cells that are located in the biliary epithelium, that oval cells are the progeny of these stem cells, and that these cells can undergo massive expansion in their numbers before differentiating into hepatocytes. This is a conditional process that 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 ability to proliferate under appropriate conditions and give rise to fully differentiated hepatocytes and other cell types.
Similar articles
-
Pluripotential liver stem cells: facultative stem cells located in the biliary tree.Cell Prolif. 1996 Jul;29(7):373-402. doi: 10.1111/j.1365-2184.1996.tb00982.x. Cell Prolif. 1996. PMID: 8883463 Review.
-
Liver stem cells: when the going gets tough they get going.Int J Exp Pathol. 1997 Dec;78(6):365-81. doi: 10.1046/j.1365-2613.1997.500375.x. Int J Exp Pathol. 1997. PMID: 9516869 Free PMC article. Review.
-
Ductular hepatocytes.Histol Histopathol. 1995 Apr;10(2):433-56. Histol Histopathol. 1995. PMID: 7599440 Review.
-
Development and molecular composition of the hepatic progenitor cell niche.Dan Med J. 2013 May;60(5):B4640. Dan Med J. 2013. PMID: 23673270 Review.
-
The role of progenitor cells in repair of liver injury and in liver transplantation.Wound Repair Regen. 2001 Nov-Dec;9(6):467-82. doi: 10.1046/j.1524-475x.2001.00467.x. Wound Repair Regen. 2001. PMID: 11896989 Review.
Cited by
-
Characterization and enrichment of hepatic progenitor cells in adult rat liver.World J Gastroenterol. 2004 May 15;10(10):1480-6. doi: 10.3748/wjg.v10.i10.1480. World J Gastroenterol. 2004. PMID: 15133858 Free PMC article.
-
Regenerative medicine: Hepatic progenitor cells up their game in the therapeutic stakes.Nat Rev Gastroenterol Hepatol. 2015 Nov;12(11):610-1. doi: 10.1038/nrgastro.2015.168. Epub 2015 Oct 6. Nat Rev Gastroenterol Hepatol. 2015. PMID: 26441248
-
Stem cells in liver regeneration and their potential clinical applications.Stem Cell Rev Rep. 2013 Oct;9(5):668-84. doi: 10.1007/s12015-013-9437-4. Stem Cell Rev Rep. 2013. PMID: 23526206 Review.
-
Molecular regulation of hepatocyte generation in adult animals.Am J Pathol. 2002 Oct;161(4):1107-10. doi: 10.1016/S0002-9440(10)64386-6. Am J Pathol. 2002. PMID: 12368183 Free PMC article. Review. No abstract available.
-
Expression and significance of histone methyltransferase SET domain containing 2 with histone H3 lysine 36 trimethylation in mouse hepatic oval cells differentiated into bile duct epithelial cells in vitro.Mol Med Rep. 2023 Mar;27(3):69. doi: 10.3892/mmr.2023.12956. Epub 2023 Feb 17. Mol Med Rep. 2023. PMID: 36799151 Free PMC article.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical