Literature DB >> 8053498

Origin and fate of oval cells in dipin-induced hepatocarcinogenesis in the mouse.

V M Factor1, S A Radaeva, S S Thorgeirsson.   

Abstract

We have studied the development and differentiation of oval cells in the Dipin model of hepatocarcinogenesis in the mouse and compared this process to generation of biliary epithelial cells by bile duct ligation using light and electron microscopy. The Dipin model of hepatocarcinogenesis consists of a single injection of an alkylating drug, Dipin (1,4-bis[N,N'-di(ethylene)-phosphamide]-piperazine), followed by partial hepatectomy. The Dipin treatment resulted in irreversible damage and gradual death of hepatocytes by necrosis and apoptosis. Earlier work provided evidence that regeneration of parenchyma occurred via oval cell proliferation and subsequent differentiation into hepatocytes that replaced the degenerating hepatocytes. Both autoradiographic and morphological data indicated that oval cells were derived from ductular cells of Hering canals. The first oval cells labeled with [3H]thymidine were similar in size and ultrastructure to ductular cells of Hering canals with whom intracellular connections existed. The proliferation of ductular cells of Hering canals gave rise to a new system of oval cell ducts that spread into the liver acinus. In the periportal areas, the transition of oval cells into hepatocytes was observed inside the ducts. Both growth patterns and ultrastructure of oval cells were different from the biliary epithelial cells in bile duct-ligated liver. Also, oval cells retained the property to interact with adjacent hepatocytes through desmosomes and intermediate junctions. Oval cell population was heterogeneous in terms of proliferating potential. A proportion of proliferating cells (38 to 45%) in the Hering canals and small oval cell ducts located in the periportal areas was similar throughout the period of oval cell development. The extent of proliferation of oval cells decreased from 62% at the stage of active migration into the acinus to 22% at maximum formation of oval cell ducts. These data suggest that in the mouse liver cells of the terminal biliary ductules harbor the hepatic stem cell compartment from which oval cells, capable of differentiating into hepatocytes, may be derived.

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Year:  1994        PMID: 8053498      PMCID: PMC1887389     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  47 in total

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Authors:  J W GRISHAM; W S HARTROFT
Journal:  Lab Invest       Date:  1961 Mar-Apr       Impact factor: 5.662

2.  Similarities in the sequence of early histological changes induced in the liver of the rat by ethionine, 2-acetylamino-fluorene, and 3'-methyl-4-dimethylaminoazobenzene.

Authors:  E FARBER
Journal:  Cancer Res       Date:  1956-02       Impact factor: 12.701

Review 3.  Role of different epithelial cell types in liver ontogenesis, regeneration and neoplasia.

Authors:  N Marceau; M J Blouin; L Germain; M Noel
Journal:  In Vitro Cell Dev Biol       Date:  1989-04

4.  Promotion of growth and differentiation of rat ductular oval cells in primary culture.

Authors:  L Germain; M Noël; H Gourdeau; N Marceau
Journal:  Cancer Res       Date:  1988-01-15       Impact factor: 12.701

Review 5.  Evidence for the stem cell origin of hepatocellular carcinoma and cholangiocarcinoma.

Authors:  S Sell; H A Dunsford
Journal:  Am J Pathol       Date:  1989-06       Impact factor: 4.307

6.  Oval cell proliferation and the origin of small hepatocytes in liver injury induced by D-galactosamine.

Authors:  J M Lemire; N Shiojiri; N Fausto
Journal:  Am J Pathol       Date:  1991-09       Impact factor: 4.307

7.  Activation of hepatic stem cell compartment in the rat: role of transforming growth factor alpha, hepatocyte growth factor, and acidic fibroblast growth factor in early proliferation.

Authors:  R P Evarts; Z Hu; K Fujio; E R Marsden; S S Thorgeirsson
Journal:  Cell Growth Differ       Date:  1993-07

8.  Autoradiography of "oval cells" appearing rapidly in the livers of rats fed N-2-fluorenylacetamide in a choline devoid diet.

Authors:  S Sell; K Osborn; H L Leffert
Journal:  Carcinogenesis       Date:  1981       Impact factor: 4.944

Review 9.  The role of determined stem-cells in the cellular lineage of hepatocellular carcinoma.

Authors:  S Sell
Journal:  Int J Dev Biol       Date:  1993-03       Impact factor: 2.203

10.  Antigenic relationship between oval cells and a subpopulation of hepatic foci, nodules, and carcinomas induced by the "resistant hepatocyte" model system.

Authors:  R A Faris; B A Monfils; H A Dunsford; D C Hixson
Journal:  Cancer Res       Date:  1991-02-15       Impact factor: 12.701

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  50 in total

1.  The facultative stem cell: A new star in liver pathology.

Authors:  Peter Nagy
Journal:  Pathol Oncol Res       Date:  1995       Impact factor: 3.201

2.  Cellular origin of regenerating parenchyma in a mouse model of severe hepatic injury.

Authors:  K M Braun; E P Sandgren
Journal:  Am J Pathol       Date:  2000-08       Impact factor: 4.307

3.  Liver damage using suicide genes. A model for oval cell activation.

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4.  The dynamics of hepatitis B virus infection.

Authors:  R J Payne; M A Nowak; B S Blumberg
Journal:  Proc Natl Acad Sci U S A       Date:  1996-06-25       Impact factor: 11.205

Review 5.  On experimental design and discourse in plasticity research.

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Journal:  Stem Cell Rev       Date:  2005       Impact factor: 5.739

Review 6.  Cellular homeostasis and repair in the mammalian liver.

Authors:  Ben Z Stanger
Journal:  Annu Rev Physiol       Date:  2015       Impact factor: 19.318

7.  Immunohistochemical study of hepatic oval cells in human chronic viral hepatitis.

Authors:  X Ma; D K Qiu; Y S Peng
Journal:  World J Gastroenterol       Date:  2001-04       Impact factor: 5.742

8.  The role of paracrine signals during liver regeneration.

Authors:  Ben Z Stanger; Linda Greenbaum
Journal:  Hepatology       Date:  2012-10       Impact factor: 17.425

9.  Triiodothyronine accelerates differentiation of rat liver progenitor cells into hepatocytes.

Authors:  Viktória László; Katalin Dezso; Kornélia Baghy; Veronika Papp; Ilona Kovalszky; Géza Sáfrány; Snorri S Thorgeirsson; Peter Nagy; Sándor Paku
Journal:  Histochem Cell Biol       Date:  2008-07-29       Impact factor: 4.304

Review 10.  Model systems and experimental conditions that lead to effective repopulation of the liver by transplanted cells.

Authors:  David A Shafritz; Michael Oertel
Journal:  Int J Biochem Cell Biol       Date:  2010-01-18       Impact factor: 5.085

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