PUBLICATION

tomm22 Knockdown-Mediated Hepatocyte Damages Elicit Both the Formation of Hybrid Hepatocytes and Biliary Conversion to Hepatocytes in Zebrafish Larvae.

Authors
Wu, J., Choi, T.Y., Shin, D.
ID
ZDB-PUB-170303-5
Date
2017
Source
Gene Expression   17(3): 237-249 (Journal)
Registered Authors
Choi, Tae-Young, Shin, Donghun
Keywords
Liver regeneration, Macrophage, Oval cells, Liver progenitor cells
MeSH Terms
  • Hepatocytes/cytology*
  • Organ Size
  • Mitochondrial Membrane Transport Proteins/genetics*
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Models, Animal
  • Cell Proliferation
  • Larva
  • Liver/injuries
  • Liver/pathology
  • Liver/physiology*
  • Cell Death
  • Biliary Tract/metabolism*
  • Oligonucleotides, Antisense/genetics
  • Zebrafish Proteins/genetics*
  • Wnt Proteins/metabolism
  • Gene Knockdown Techniques
  • beta Catenin/metabolism
  • Signal Transduction
  • Animals, Genetically Modified
  • Liver Regeneration*
  • Macrophages/cytology
  • Animals
  • Green Fluorescent Proteins/metabolism
(all 24)
PubMed
28251883 Full text @ Gene Expr.
Abstract
The liver has a highly regenerative capacity. In the normal liver, hepatocytes proliferate to restore lost liver mass.However, when hepatocyte proliferation is impaired, biliary epithelial cells (BECs) activate and contribute to hepatocytes. We previously reported in zebrafish that upon severe hepatocyte ablation, BECs extensively contribute to regenerated hepatocytes. It was also speculated that BECdriven liver regeneration might occur in another zebrafish liver injury model in which temporary knockdown of the mitochondrial import gene tomm22 by morpholino antisense oligonucleotides (MO) induces hepatocyte death. Given the importance of multiple BEC-driven liver regeneration models for better elucidating the mechanisms underlying innate liver regeneration in the diseased liver, we hypothesized that BECs would contribute to hepatocytes in tomm22 MO-injected larvae. In this MO-based liver injury model, by tracing the lineage of BECs, we found that BECs significantly contributed to hepatocytes. Moreover, we found that surviving, pre-existing hepatocytes become BEC-hepatocyte hybrid cells in tomm22 MO-injected larvae. Intriguingly, both the inhibition of Wnt/β-catenin signaling and macrophage ablation suppressed the formation of the hybrid hepatocytes. This new liver injury model in which both hepatocytes and BECs contribute to regenerated hepatocytes will aid in better understanding the mechanisms of innate liver regeneration in the diseased liver.
Genes / Markers
Figures
Figure Gallery (6 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
as3TgTransgenic Insertion
    c264TgTransgenic Insertion
      cz1701TgTransgenic Insertion
        gl24TgTransgenic Insertion
          kyu1TgTransgenic Insertion
            pt608TgTransgenic Insertion
              s931TgTransgenic Insertion
                s939TgTransgenic Insertion
                  s959TgTransgenic Insertion
                    uwm12TgTransgenic Insertion
                      1 - 10 of 10
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                      Human Disease / Model
                      No data available
                      Sequence Targeting Reagents
                      Target Reagent Reagent Type
                      tomm22MO1-tomm22MRPHLNO
                      1 - 1 of 1
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                      Fish
                      Antibodies
                      Orthology
                      No data available
                      Engineered Foreign Genes
                      Marker Marker Type Name
                      CFPEFGCFP
                      CreEFGCre
                      d2EGFPEFGd2EGFP
                      Dendra2EFGDendra2
                      ECFPEFGECFP
                      EGFPEFGEGFP
                      GAL4EFGGAL4
                      mAGFPEFGmAGFP
                      mCherryEFGmCherry
                      NTREFGNTR
                      1 - 10 of 10
                      Show
                      Mapping
                      No data available