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  4. Oval cell proliferation in p16INK4a expressing mouse liver is triggered by chronic growth stimuli
 
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2008
Journal Article
Title

Oval cell proliferation in p16INK4a expressing mouse liver is triggered by chronic growth stimuli

Abstract
Terminal differentiation requires molecules also involved in aging such as the cell cycle inhibitor p16INK4a.Like other organs, the adult liver represents a quiescent organ with terminal differentiated cells, hepatocytes and cholangiocytes. These cells retain the ability to proliferate in response to liver injury or reduction of liver mass. However, under conditions which prevent mitotic activation of hepatocytes, regeneration can occur instead from facultative hepatic stem cells.For therapeutic application a non-toxic activation of this stem cell compartment is required. We have established transgenic mice with conditional overexpression of the cell cycle inhibitor p16INK4a in hepatocytes and have provoked and examined oval cell activation in adult liver in response to a range of proliferative stimuli.We could show that the liver specific expression of p16INK4a leads to a faster differentiation of hepatocytes and an activation of oval cells already in postnatal mice without negative consequences on liver function.
Author(s)
Ueberham, Elke
Universität Leipzig
Lindner, Ricco
Universität Leipzig
Kamprad, Manja
Universität Leipzig
Hiemann, Rico
Universität Leipzig
Hilger, Nadja
Universität Leipzig
Woithe, Barbara
Universität Leipzig
Mahn, Doris
Universität Leipzig
Cross, Michael
Universität Leipzig
Sack, Ulrich
Universität Leipzig
Gebhardt, Rolf
Universität Leipzig
Arendt, Thomas
Universität Leipzig
Ueberham, Uwe
Universität Leipzig
Journal
Journal of cellular and molecular medicine  
Open Access
DOI
10.1111/j.1582-4934.2007.00178.x
Additional link
Full text
Language
English
Fraunhofer-Institut für Zelltherapie und Immunologie IZI  
Keyword(s)
  • hepatic stem cell

  • Nodularin

  • starvation

  • Tet-system

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