Pseudo-dynamic analysis of heart tube formation in the mouse reveals strong regional variability and early left-right asymmetry

2021 ◽  
Author(s):  
Yen Tran
2021 ◽  
Author(s):  
Isaac Esteban ◽  
Patrick Schmidt ◽  
Susana Temino ◽  
Leif Kobbelt ◽  
Miguel Torres

Understanding organ morphogenesis requires a precise geometrical description of the tissues involved in the process. In highly regulative embryos, like those of mammals, morphological variability hinders the quantitative analysis of morphogenesis. In particular, the study of early heart development in mammals remains a challenging problem, due to imaging limitations and innate complexity. Around embryonic day 7.5 (E7.5), the cardiac crescent folds in an intricate and coordinated manner to produce a pumping linear heart tube at E8.25, followed by heart looping at E8.5. In this work we provide a complete morphological description of this process based on detailed imaging of a temporally dense collection of embryonic heart morphologies. We apply new approaches for morphometric staging and quantification of local morphological variations between specimens at the same stage. We identify hot spots of regionalized variability and identify left-right asymmetry in the inflow region starting at the late cardiac crescent stage, which represents the earliest signs of organ left-right asymmetry in the mammalian embryo. Finally, we generate a 3D+t digital model that provides a framework suitable for co-representation of data from different sources and for the computer modelling of the process.


2008 ◽  
Vol 102 (2) ◽  
Author(s):  
Stefan Rohr ◽  
Cécile Otten ◽  
Salim Abdelilah-Seyfried

Development ◽  
2021 ◽  
Author(s):  
Cristiana Dondi ◽  
Benjamin Bertin ◽  
Jean-Philippe Daponte ◽  
Inga Wojtowicz ◽  
Krzysztof Jagla ◽  
...  

The formation of the cardiac tube is a remarkable example of complex morphogenetic processes conserved from invertebrates to humans. It involves coordinated collective migration of contralateral rows of cardiac cells. The molecular processes underlying the specification of cardioblasts (CBs) prior to migration are well established and significant advances have been made in understanding the process of lumen formation. However, the mechanisms of collective cardiac cells migration remain elusive. Here we identified CAP and MSP300 as novel actors involved during CBs migration. They both exhibit highly similar temporal and spatial expression patterns in migrating cardiac cells and are necessary for the correct number and alignment of CBs, a prerequisite for the coordination of their collective migration. Our data suggest that CAP and MSP300 are part of a protein complex linking focal adhesion sites to nuclei via the actin cytoskeleton that maintains post-mitotic state and correct alignment of CBs.


1997 ◽  
Vol 11 (8) ◽  
pp. 1061-1072 ◽  
Author(s):  
J D Molkentin ◽  
Q Lin ◽  
S A Duncan ◽  
E N Olson

genesis ◽  
2007 ◽  
Vol 45 (11) ◽  
pp. 667-678 ◽  
Author(s):  
Daniel D. Brown ◽  
Kathleen S. Christine ◽  
Christopher Showell ◽  
Frank L. Conlon

2010 ◽  
Vol 344 (1) ◽  
pp. 433 ◽  
Author(s):  
Stephanie Woo ◽  
Jason E. Fish ◽  
Joshua D. Wythe ◽  
Benoit B. Bruneau ◽  
Didier Y. Stainier ◽  
...  

1997 ◽  
Vol 11 (8) ◽  
pp. 1048-1060 ◽  
Author(s):  
C T Kuo ◽  
E E Morrisey ◽  
R Anandappa ◽  
K Sigrist ◽  
M M Lu ◽  
...  

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