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Loss of hepatocyte ...
Loss of hepatocyte cell division leads to liver inflammation and fibrosis
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- Dewhurst, Matthew R (författare)
- University of Manchester,A*Star Institute of Molecular and Cell Biology (IMCB)
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- Ow, Jin Rong (författare)
- A*Star Institute of Molecular and Cell Biology (IMCB)
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- Zafer, Gözde (författare)
- National University of Singapore,A*Star Institute of Molecular and Cell Biology (IMCB)
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- van Hul, Noémi K M (författare)
- A*Star Institute of Molecular and Cell Biology (IMCB)
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- Wollmann, Heike (författare)
- A*Star Institute of Molecular and Cell Biology (IMCB)
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- Bisteau, Xavier (författare)
- A*Star Institute of Molecular and Cell Biology (IMCB)
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- Brough, David (författare)
- Manchester Metropolitan University
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- Choi, Hyungwon (författare)
- A*Star Institute of Molecular and Cell Biology (IMCB)
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- Kaldis, Philipp (författare)
- Lund University,Lunds universitet,Diabetiska komplikationer,Forskargrupper vid Lunds universitet,Metabolism och leversjukdomar,Diabetic Complications,Lund University Research Groups,Metabolic disorders and liver disease,National University of Singapore,A*Star Institute of Molecular and Cell Biology (IMCB)
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(creator_code:org_t)
- 2020-11-04
- 2020
- Engelska.
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Ingår i: PLoS Genetics. - : Public Library of Science (PLoS). - 1553-7404. ; 16:11, s. 1009084-1009084
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Abstract
Ämnesord
Stäng
- The liver possesses a remarkable regenerative capacity based partly on the ability of hepatocytes to re-enter the cell cycle and divide to replace damaged cells. This capability is substantially reduced upon chronic damage, but it is not clear if this is a cause or consequence of liver disease. Here, we investigate whether blocking hepatocyte division using two different mouse models affects physiology as well as clinical liver manifestations like fibrosis and inflammation. We find that in P14 Cdk1Liv-/- mice, where the division of hepatocytes is abolished, polyploidy, DNA damage, and increased p53 signaling are prevalent. Cdk1Liv-/- mice display classical markers of liver damage two weeks after birth, including elevated ALT, ALP, and bilirubin levels, despite the lack of exogenous liver injury. Inflammation was further studied using cytokine arrays, unveiling elevated levels of CCL2, TIMP1, CXCL10, and IL1-Rn in Cdk1Liv-/- liver, which resulted in increased numbers of monocytes. Ablation of CDK2-dependent DNA re-replication and polyploidy in Cdk1Liv-/- mice reversed most of these phenotypes. Overall, our data indicate that blocking hepatocyte division induces biological processes driving the onset of the disease phenotype. It suggests that the decrease in hepatocyte division observed in liver disease may not only be a consequence of fibrosis and inflammation, but also a pathological cue.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Gastroenterologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Gastroenterology and Hepatology (hsv//eng)
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
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