header logo image header logo text
Downloads Login
Research
General Information
ZIRC
ZFIN ID: ZDB-PUB-161110-11
EphrinB1/EphB3b Coordinate Bidirectional Epithelial-Mesenchymal Interactions Controlling Liver Morphogenesis and Laterality
Cayuso, J., Dzementsei, A., Fischer, J.C., Karemore, G., Caviglia, S., Bartholdson, J., Wright, G.J., Ober, E.A.
Date: 2016
Source: Developmental Cell 39: 316-328 (Journal)
Registered Authors: Caviglia, Sara, Dzementsei, Aliaksandr, Fischer, Johanna, Ober, Elke, Wright, Gavin J.
Keywords: EphB3, EphrinB1, bidirectional, lateral plate mesoderm, liver, migration, morphogenesis, protrusion, repulsion, zebrafish
MeSH Terms:
  • Animals
  • Body Patterning
  • Cell Movement
  • Cell Shape
  • Ephrin-B1/metabolism*
  • Ephrin-B3/metabolism*
  • Epithelium/embryology*
  • Epithelium/metabolism
  • Functional Laterality*
  • Liver/embryology*
  • Mesoderm/embryology*
  • Mesoderm/metabolism
  • Morphogenesis*
  • Pseudopodia/metabolism
  • Receptors, Eph Family/metabolism*
  • Zebrafish/embryology
  • Zebrafish/metabolism
  • Zebrafish Proteins/metabolism*
PubMed: 27825440 Full text @ Dev. Cell
FIGURES
ABSTRACT
Positioning organs in the body often requires the movement of multiple tissues, yet the molecular and cellular mechanisms coordinating such movements are largely unknown. Here, we show that bidirectional signaling between EphrinB1 and EphB3b coordinates the movements of the hepatic endoderm and adjacent lateral plate mesoderm (LPM), resulting in asymmetric positioning of the zebrafish liver. EphrinB1 in hepatoblasts regulates directional migration and mediates interactions with the LPM, where EphB3b controls polarity and movement of the LPM. EphB3b in the LPM concomitantly repels hepatoblasts to move leftward into the liver bud. Cellular protrusions controlled by Eph/Ephrin signaling mediate hepatoblast motility and long-distance cell-cell contacts with the LPM beyond immediate tissue interfaces. Mechanistically, intracellular EphrinB1 domains mediate EphB3b-independent hepatoblast extension formation, while EpB3b interactions cause their destabilization. We propose that bidirectional short- and long-distance cell interactions between epithelial and mesenchyme-like tissues coordinate liver bud formation and laterality via cell repulsion.
ADDITIONAL INFORMATION