Literature DB >> 9141427

Expression of alpha-fetoprotein and stem cell factor/c-kit system in bile duct ligated young rats.

M Omori1, R P Evarts, N Omori, Z Hu, E R Marsden, S S Thorgeirsson.   

Abstract

The existence of a facultative hepatic stem cell compartment in bile ductules that participates in the renewal process of epithelial cell populations in the liver is well documented. The present study was undertaken to determine whether the immature bile epithelium responds differently to growth stimulus induced by bile stasis to that seen in the adult animal. In addition, the possible involvement of the growth factor/receptor systems associated with early activation of hepatic stem cells in bile duct proliferation was also examined. Bile duct ligation was used to induce the proliferation of bile epithelial cells. The expression of full-length alpha-fetoprotein (AFP) was used as an indicator for activation of the stem cell compartment. AFP was highly and selectively expressed in small bile ducts 7 days after bile duct ligation in immature rats up to 5 weeks of age. Although no significant increase in the expression of stem cell factor (SCF) c-kit, hepatocyte growth factor (HGF), and transforming growth factor-alpha (TGF-alpha) was observed 7 days after bile duct ligation in adult rats, the expression of all these growth factors was increased in bile duct ligated rats up to 5 weeks of age. These results suggest that the bile ductular epithelium in the young rats responds to bile stasis in a fashion that is phenotypically similar to that seen during early activation of hepatic stem cells in adult liver.

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Year:  1997        PMID: 9141427     DOI: 10.1002/hep.510250512

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  13 in total

1.  Paracrine modulation of cholangiocyte serotonin synthesis orchestrates biliary remodeling in adults.

Authors:  Alessia Omenetti; Liu Yang; Raul R Gainetdinov; Cynthia D Guy; Steve S Choi; Wei Chen; Marc G Caron; Anna Mae Diehl
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2010-11-11       Impact factor: 4.052

2.  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

Review 3.  Wound healing in the liver with particular reference to stem cells.

Authors:  M Alison; M Golding; C Sarraf
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1998-06-29       Impact factor: 6.237

4.  Gadolinium chloride suppresses hepatic oval cell proliferation in rats with biliary obstruction.

Authors:  J K Olynyk; G C Yeoh; G A Ramm; S L Clarke; P M Hall; R S Britton; B R Bacon; T F Tracy
Journal:  Am J Pathol       Date:  1998-02       Impact factor: 4.307

5.  Identification of genes specific to "oval cells" in the rat 2-acetylaminofluorene/partial hepatectomy model.

Authors:  Danko S Batusic; Velasco Cimica; Yonglong Chen; Kyrylo Tron; Thomas Hollemann; Tomas Pieler; Giuliano Ramadori
Journal:  Histochem Cell Biol       Date:  2005-10-28       Impact factor: 4.304

6.  Thy1-positive bone marrow stem cells express liver-specific genes in vitro and can mature into hepatocytes in vivo.

Authors:  Si Hyun Bae; Jong Young Choi; Seung Kew Yoon; Il-Hoan Oh; Kun Ho Yoon; Seong Tae Park; Gi Dae Kim; Seh-Hoon Oh; Bryon E Petersen
Journal:  Hepatol Int       Date:  2007-11-27       Impact factor: 6.047

7.  Bile Duct Ligation Induces ATZ Globule Clearance in a Mouse Model of α-1 Antitrypsin Deficiency.

Authors:  Zahida Khan; Shinichiro Yokota; Yoshihiro Ono; Aaron W Bell; Michael Oertel; Donna B Stolz; George K Michalopoulos
Journal:  Gene Expr       Date:  2016-08-18

8.  Stem cell factor restores hepatocyte proliferation in IL-6 knockout mice following 70% hepatectomy.

Authors:  Xiaodan Ren; Cory Hogaboam; Audra Carpenter; Lisa Colletti
Journal:  J Clin Invest       Date:  2003-11       Impact factor: 14.808

Review 9.  The Sea Lamprey as an Etiological Model for Biliary Atresia.

Authors:  Yu-Wen Chung-Davidson; Chu-Yin Yeh; Weiming Li
Journal:  Biomed Res Int       Date:  2015-05-26       Impact factor: 3.411

10.  KIT is required for hepatic function during mouse post-natal development.

Authors:  Laetitia Magnol; Marie-Clémence Chevallier; Valérie Nalesso; Stéphanie Retif; Helmut Fuchs; Martina Klempt; Patricia Pereira; Michel Riottot; Sandra Andrzejewski; Bich-Thuy Doan; Jean-Jacques Panthier; Anne Puech; Jean-Claude Beloeil; Martin Hrabe de Angelis; Yann Hérault
Journal:  BMC Dev Biol       Date:  2007-07-05       Impact factor: 1.978

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