Abstract

In the embryonic heart development of mammals and birds, a straight initial heart tube undergoes left-handed helical looping, which is a remarkable and puzzling event. We are interested in the mechanism of this chiral helical looping. Recently, observations were reported that myocardial cells in the embryonic chick heart show intrinsic chirality of rotation. The chirality of myocardial cells, via anisotropic polarization of Golgi inside the cells, leads to a left-right (LR) asymmetry of cell shape. On cell boundaries of LR asymmetric cells, phosphorylated myosin and N-cadherin are enriched. Such LR asymmetric cellular circumstances lead to a large-scale three-dimensional chiral structure, the left-handed helical loop. However, the physical mechanism of this looping is unclear. Computer simulations were performed using a cell-based three-dimensional mathematical model assuming an anterior-rightward-biased contractile force of the cell boundaries on the ventral surface of the heart (orientation of a clock hand pointing to 10 to 11 o’clock). An initially straight heart tube was successfully remodeled to the left-handed helical tube via frequent convergent extension (CE) of collective cells, which corresponds to the previously reported observations of chick heart development. Although we assumed that the biased boundary contractile force was uniform all over the ventral side, orientations of the CEs became position specific on the anterior, posterior, right, and left regions on the ventral tube. Such position-specific CEs produced the left-handed helical loop. In addition, our results suggest the loop formation process consists of two distinct phases of preparation and explicit looping. Intrinsic cell properties of chirality in this investigation were discussed relating to extrinsic factors investigated by other researches. Finally, because CE is generally exerted in the axial developmental process across different animal species, we discussed the contribution of CE to the chiral heart structure across species of chick, mouse, Xenopus, and zebrafish.

Highlights

  • In mammals and birds, embryonic development of the heart involves the conversion of a straight tubular structure into a three-dimensional (3D) left-handed helical loop

  • Contractile force of specific edges was assumed; that is, that edges whose directions are close to the vertical direction have strong contractile force and the change in the polygonal pattern was examined by using a mathematical model system

  • convergent extension (CE) caused by the anisotropic contractile force of edges was demonstrated at the cellular level by computer simulation of the mathematical model [20,21]

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Summary

Introduction

Embryonic development of the heart involves the conversion of a straight tubular structure into a three-dimensional (3D) left-handed helical loop. The structure and morphogenesis of heart looping have been investi-. Heart looping is a mechanical event, and we were interested in the mechanism determining handedness. Cardiac looping in mammals and birds was first identified a century ago [8,9,10]. Patten [10] proposed that looping results from a buckling mechanism in a tube elongating between fixed poles. Heart looping was observed to form through a combination of ventral bending and rightward rotation [11]. Helical looping definitively distinguished from simple bending was reported to form through the combination of ventral

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