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Signals from dying hepatocytes trigger growth of liver progenitors.

ABSTRACT: The death rate of mature hepatocytes is chronically increased in various liver diseases, triggering responses that prevent liver atrophy, but often cause fibrosis. Mice with targeted disruption of inhibitor kappa B kinase (Ikk) in hepatocytes (HEP mice) provide a model to investigate this process because inhibiting Ikk-nuclear factor-kappaB (NF-kappaB) signalling in hepatocytes increases their apoptosis.Cell proliferation, apoptosis, progenitors, fibrosis and production of Hedgehog (Hh) ligands (progenitor and myofibroblast growth factors) were compared in HEP and control mice before and after feeding methionine choline-deficient ethionine-supplemented (MCDE) diets. Ikkbeta was deleted from primary hepatocytes to determine the effects on Hh ligand production; Hh signalling was inhibited directly in progenitors to determine the effects on viability. Liver sections from patients were examined to assess relationships between hepatocyte production of Hh ligands, accumulation of myofibroblastic cells and liver fibrosis.Disrupting the Ikk-NF-kappaB pathway in hepatocytes inhibited their proliferation but induced their production of Hh ligands. The latter provided viability signals for progenitors and myofibroblasts, enhancing accumulation of these cell types and causing fibrogenesis. Findings in the mouse models were recapitulated in diseased human livers.Dying mature hepatocytes produce Hh ligands which promote the compensatory outgrowth of progenitors and myofibroblasts. These results help to explain why diseases that chronically increase hepatocyte death promote cirrhosis.

SUBMITTER: Jung Y

PROVIDER: S-EPMC3632642 | biostudies-literature | 2010 May

REPOSITORIES: biostudies-literature

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Signals from dying hepatocytes trigger growth of liver progenitors.

Jung Youngmi Y Witek Rafal P RP Syn Wing-Kin WK Choi Steve S SS Omenetti Alessia A Premont Richard R Guy Cynthia D CD Diehl Anna Mae AM

Gut 20100501 5

<h4>Objective</h4>The death rate of mature hepatocytes is chronically increased in various liver diseases, triggering responses that prevent liver atrophy, but often cause fibrosis. Mice with targeted disruption of inhibitor kappa B kinase (Ikk) in hepatocytes (HEP mice) provide a model to investigate this process because inhibiting Ikk-nuclear factor-kappaB (NF-kappaB) signalling in hepatocytes increases their apoptosis.<h4>Methods</h4>Cell proliferation, apoptosis, progenitors, fibrosis and pr ...[more]

PMID: 20427400

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Signals from dying hepatocytes trigger growth of liver progenitors.

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Signals from dying hepatocytes trigger growth of liver progenitors.

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