arrow
Return

A morphogenetic EphB/EphrinB code controls hepatopancreatic duct formation

delete2019-11-19
delete15
delete
OA
AI
M
M. Ilcim Thestrup
S
Sara Caviglia
J
Jordi Cayuso
R
Ronja L. S. Heyne
R
Racha Ahmad
W
Wolfgang Hofmeister
L
Letizia Satriano
D
David G. Wilkinson
J
Jesper B. Andersen
E
Elke A. Ober *
DOI:10.1038/s41467-019-13149-7delete
deleteOriginal
deleteShare
deleteSave
View PDF
Abstract

Abstract

En 中文
The hepatopancreatic ductal (HPD) system connects the intrahepatic and intrapancreatic ducts to the intestine and ensures the afferent transport of the bile and pancreatic enzymes. Yet the molecular and cellular mechanisms controlling their differentiation and morphogenesis into a functional ductal system are poorly understood. Here, we characterize HPD system morphogenesis by high-resolution microscopy in zebrafish. The HPD system differentiates from a rod of unpolarized cells into mature ducts by de novo lumen formation in a dynamic multi-step process. The remodeling step from multiple nascent lumina into a single lumen requires active cell intercalation and myosin contractility. We identify key functions for EphB/EphrinB signaling in this dynamic remodeling step. Two EphrinB ligands, EphrinB1 and EphrinB2a, and two EphB receptors, EphB3b and EphB4a, control HPD morphogenesis by remodeling individual ductal compartments, and thereby coordinate the morphogenesis of this multi-compartment ductal system.
Keywords:
LUMEN FORMATION
BILIARY SYSTEM
BILE-DUCT
TOXIN BILIATRESONE
EPH RECEPTOR
ZEBRAFISH
TISSUE
KINASE
TUBULOGENESIS
MECHANISMS
AI Summary

AI Summary

Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.

Journal

Nature Communications cover
Nature Communications
IF:
15.7
Papers:
9.2W
Citations:
91.2W

Organization

U
University of Copenhagen
Scholars:
7.6W
Papers: 6.6W
Citations: 86
F
Francis Crick Institute
Scholars:
4.3K
Papers: 2.4K
Citations: 8.9K
U
University of Southern Denmark
Scholars:
2.1W
Papers: 2.0W
Citations: 2.9W
researcher View more organizations