Primary cilia are critical for tracheoesophageal septation

Introduction Primary cilia play pivotal roles in the patterning and morphogenesis of a wide variety of organs during mammalian development. Here we examined murine foregut septation in the cobblestone mutant, a hypomorphic allele of the gene encoding the intraflagellar transport protein IFT88, a pro...

Full description

Saved in:
Bibliographic Details
Main Authors: Avery Fitzsimons, Lindsey (Author) , Tasouri, Evangelia (Author) , Willaredt, Marc August (Author) , Stetson, Daniel (Author) , Gojak, Christian (Author) , Kirsch, Joachim (Author) , Gardner, Humphrey A. R. (Author) , Gorgas, Karin (Author) , Tucker, Kerry L. (Author)
Format: Article (Journal)
Language:English
Published: 2023
In: Developmental dynamics
Year: 2023, Pages: 1-21
ISSN:1097-0177
DOI:10.1002/dvdy.660
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/dvdy.660
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/dvdy.660
Get full text
Author Notes:Lindsey Avery Fitzsimons, Evangelia Tasouri, Marc August Willaredt, Daniel Stetson, Christian Gojak, Joachim Kirsch, Humphrey A.R. Gardner, Karin Gorgas, Kerry L. Tucker
Description
Summary:Introduction Primary cilia play pivotal roles in the patterning and morphogenesis of a wide variety of organs during mammalian development. Here we examined murine foregut septation in the cobblestone mutant, a hypomorphic allele of the gene encoding the intraflagellar transport protein IFT88, a protein essential for normal cilia function. Results We reveal a crucial role for primary cilia in foregut division, since their dramatic decrease in cilia in both the foregut endoderm and mesenchyme of mutant embryos resulted in a proximal tracheoesophageal septation defects and in the formation of distal tracheo(broncho)esophageal fistulae similar to the most common congenital tracheoesophageal malformations in humans. Interestingly, the dorsoventral patterning determining the dorsal digestive and the ventral respiratory endoderm remained intact, whereas Hedgehog signaling was aberrantly activated. Conclusions Our results demonstrate the cobblestone mutant to represent one of the very few mouse models that display both correct endodermal dorsoventral specification but defective compartmentalization of the proximal foregut. It stands exemplary for a tracheoesophageal ciliopathy, offering the possibility to elucidate the molecular mechanisms how primary cilia orchestrate the septation process. The plethora of malformations observed in the cobblestone embryo allow for a deeper insight into a putative link between primary cilia and human VATER/VACTERL syndromes.
Item Description:Vorab online veröffentlicht: 30. September 2023
Gesehen am 09.11.2023
Physical Description:Online Resource
ISSN:1097-0177
DOI:10.1002/dvdy.660