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
-
- Animals
- Fibroblast Growth Factors/physiology
- Hepatopancreas/embryology*
- Hepatopancreas/physiology
- Islets of Langerhans/physiology*
- Pancreas/cytology
- Pancreas/physiology
- Receptors, Notch/physiology
- Regeneration
- SOX9 Transcription Factor/physiology*
- Signal Transduction
- Zebrafish/embryology*
- Zebrafish/physiology
- Zebrafish Proteins/physiology*
- PubMed
- 22537488 Full text @ Dev. Biol.
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.