PUBLICATION

Zebrafish sox9b is crucial for hepatopancreatic duct development and pancreatic endocrine cell regeneration

Authors
Manfroid, I., Ghaye, A., Naye, F., Detry, N., Palm, S., Pan, L., Ma, T.P., Huang, W., Rovira, M., Martial, J.A., Parsons, M.J., Moens, C.B., Voz, M.L., and Peers, B.
ID
ZDB-PUB-120430-10
Date
2012
Source
Developmental Biology   366(2): 268-278 (Journal)
Registered Authors
Huang, Wei, Manfroid, Isabelle, Martial, Joseph A., Ma, Taylur, Moens, Cecilia, Pan, Luyuan, Parsons, Michael, Peers, Bernard, Voz, Marianne
Keywords
duct, beta cell regeneration, pancreas, sox9, notch, FGF
MeSH Terms
  • Hepatopancreas/embryology*
  • Hepatopancreas/physiology
  • Animals
  • Signal Transduction
  • Receptors, Notch/physiology
  • Pancreas/cytology
  • Pancreas/physiology
  • SOX9 Transcription Factor/physiology*
  • Zebrafish/embryology*
  • Zebrafish/physiology
  • Regeneration
  • Fibroblast Growth Factors/physiology
  • Islets of Langerhans/physiology*
  • Zebrafish Proteins/physiology*
(all 14)
PubMed
22537488 Full text @ Dev. Biol.
Abstract

Recent zebrafish studies have shown that the late appearing pancreatic endocrine cells are derived from pancreatic ducts but the regulatory factors involved are still largely unknown. Here, we show that the zebrafish sox9b gene is expressed in pancreatic ducts where it labels the pancreatic Notch-responsive cells previously shown to be progenitors. Inactivation of sox9b disturbs duct formation and impairs regeneration of beta cells from these ducts in larvae. sox9b expression in the midtrunk endoderm appears at the junction of the hepatic and ventral pancreatic buds and, by the end of embryogenesis, labels the hepatopancreatic ductal system as well as the intrapancreatic and intrahepatic ducts. Ductal morphogenesis and differentiation are specifically disrupted in sox9b mutants, with the dysmorphic hepatopancreatic ducts containing misdifferentiated hepatocyte-like and pancreatic-like cells. We also show that maintenance of sox9b expression in the extrapancreatic and intrapancreatic ducts requires FGF and Notch activity, respectively, both pathways known to prevent excessive endocrine differentiation in these ducts. Furthermore, beta cell recovery after specific ablation is severely compromised in sox9b mutant larvae. Our data position sox9b as a key player in the generation of secondary endocrine cells deriving from pancreatic ducts in zebrafish.

Genes / Markers
Figures
Figure Gallery (8 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
b971
    Deficiency
    fh313
      Point Mutation
      jh1TgTransgenic Insertion
        jh4TgTransgenic Insertion
          jh11TgTransgenic Insertion
            t22030
              Point Mutation
              tbvbo
                Point Mutation
                1 - 7 of 7
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                Human Disease / Model
                No data available
                Sequence Targeting Reagents
                Target Reagent Reagent Type
                bmp2aMO3-bmp2aMRPHLNO
                1 - 1 of 1
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                Fish
                Antibodies
                Name Type Antigen Genes Isotypes Host Organism
                ab1-hnf4apolyclonalIgGGoat
                Ab1-pdx1polyclonalGuinea pig
                Ab1-sox9polyclonal
                  Rabbit
                  Ab-2F11monoclonalIgG1Mouse
                  Ab2-nkx6monoclonalIgG1Mouse
                  Ab2-pax6polyclonalRabbit
                  Ab3-prox1polyclonalRabbit
                  1 - 7 of 7
                  Show
                  Orthology
                  No data available
                  Engineered Foreign Genes
                  Marker Marker Type Name
                  EGFPEFGEGFP
                  mCherryEFGmCherry
                  NTREFGNTR
                  1 - 3 of 3
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                  Mapping
                  No data available