EphrinB1/EphB3b Coordinate Bidirectional Epithelial-Mesenchymal Interactions Controlling Liver Morphogenesis and Laterality
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EphrinB1/EphB3b Coordinate Bidirectional Epithelial-Mesenchymal Interactions Controlling Liver Morphogenesis and Laterality. / Cayuso, Jordi; Dzementsei, Aliaksandr; Fischer, Johanna C; Karemore, Gopal; Caviglia, Sara; Bartholdson, Josefin; Wright, Gavin J; Ober, Elke A.
In: Developmental Cell, Vol. 39, No. 3, 07.11.2016, p. 316-328.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - EphrinB1/EphB3b Coordinate Bidirectional Epithelial-Mesenchymal Interactions Controlling Liver Morphogenesis and Laterality
AU - Cayuso, Jordi
AU - Dzementsei, Aliaksandr
AU - Fischer, Johanna C
AU - Karemore, Gopal
AU - Caviglia, Sara
AU - Bartholdson, Josefin
AU - Wright, Gavin J
AU - Ober, Elke A
N1 - Copyright © 2016. Published by Elsevier Inc.
PY - 2016/11/7
Y1 - 2016/11/7
N2 - 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.
AB - 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.
U2 - 10.1016/j.devcel.2016.10.009
DO - 10.1016/j.devcel.2016.10.009
M3 - Journal article
C2 - 27825440
VL - 39
SP - 316
EP - 328
JO - Developmental Cell
JF - Developmental Cell
SN - 1534-5807
IS - 3
ER -
ID: 169010424