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ZIRC
ZFIN ID: ZDB-PUB-050623-3
Exocrine pancreas development in zebrafish
Yee, N.S., Lorent, K., and Pack, M.
Date: 2005
Source: Developmental Biology   284(1): 84-101 (Journal)
Registered Authors: Lorent, Kristin, Pack, Michael, Yee, Nelson S.
Keywords: Exocrine pancreas; Zebrafish; Development; Duct; Acinus; Jagged; Notch
MeSH Terms:
  • Animals
  • Calcium-Binding Proteins/genetics
  • Cell Differentiation/physiology*
  • Endoderm/physiology
  • Immunohistochemistry
  • In Situ Hybridization
  • Intercellular Signaling Peptides and Proteins
  • Membrane Proteins/genetics
  • Microscopy, Electron, Transmission
  • Models, Biological*
  • Morphogenesis/physiology*
  • Mutagenesis
  • Pancreas/embryology*
  • Pancreas/ultrastructure
  • Signal Transduction/physiology*
  • Ubiquitin-Protein Ligases/genetics
  • Zebrafish/embryology*
  • Zebrafish Proteins/genetics
PubMed: 15963491 Full text @ Dev. Biol.
FIGURES
ABSTRACT
Although many of the genes that regulate development of the endocrine pancreas have been identified, comparatively little is known about how the exocrine pancreas forms. Previous studies have shown that exocrine pancreas development may be modeled in zebrafish. However, the timing and mechanism of acinar and ductal differentiation and morphogenesis have not been described. Here, we characterize zebrafish exocrine pancreas development in wild type and mutant larvae using histological, immunohistochemical and ultrastructural analyses. These data allow us to identify two stages of zebrafish exocrine development. During the first stage, the exocrine anlage forms from rostral endodermal cells. During the second stage, protodifferentiated progenitor cells undergo terminal differentiation followed by acinar gland and duct morphogenesis. Immunohistochemical analyses support a model in which the intrapancreatic ductal system develops from progenitors that join to form a contiguous network rather than by branching morphogenesis of the pancreatic epithelium, as described for mammals. Contemporaneous appearance of acinar glands and ducts in developing larvae and their disruption in pancreatic mutants suggest that common molecular pathways may regulate gland and duct morphogenesis and differentiation of their constituent cells. By contrast, analyses of mind bomb mutants and jagged morpholino-injected larvae suggest that Notch signaling principally regulates ductal differentiation of bipotential exocrine progenitors.
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