Laboratory for Developmental Morphogeometry, RIKEN Center for Biosystems Dynamics Research, Kobe 650-0047, Japan; Department of Anatomy and Cell Biology, Graduate School of Medicine, Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Laboratory for Developmental Morphogeometry, RIKEN Center for Biosystems Dynamics Research, Kobe 650-0047, Japan.
Cell Rep. 2020 Mar 17;30(11):3889-3903.e5. doi: 10.1016/j.celrep.2020.02.071.
Despite extensive study, the morphogenetic mechanisms of heart looping remain controversial because of a lack of information concerning precise tissue-level deformation and the quantitative relationship between tissue and cellular dynamics; this lack of information causes difficulties in evaluating previously proposed models. To overcome these limitations, we perform four-dimensional (4D) high-resolution imaging to reconstruct a tissue deformation map, which reveals that, at the tissue scale, initial heart looping is achieved by left-right (LR) asymmetry in the direction of deformation within the myocardial tube. We further identify F-actin-dependent directional cell rearrangement in the right myocardium as a major contributor to LR asymmetric tissue deformation. Our findings demonstrate that heart looping involves dynamic and intrinsic cellular behaviors within the tubular tissue and provide a significantly different viewpoint from current models that are based on LR asymmetry of growth and/or stress at the tube boundaries. Finally, we propose a minimally sufficient model for initial heart looping that is also supported by mechanical simulations.
尽管进行了广泛的研究,但由于缺乏有关精确组织层面变形的信息以及组织和细胞动力学之间的定量关系,心脏环曲的形态发生机制仍然存在争议;这种信息的缺乏导致难以评估先前提出的模型。为了克服这些限制,我们进行了四维(4D)高分辨率成像以重建组织变形图,该图显示,在组织尺度上,最初的心脏环曲是通过心肌管内变形方向的左右(LR)不对称来实现的。我们进一步确定 F-肌动蛋白依赖性的右心肌细胞定向重排是 LR 不对称组织变形的主要贡献者。我们的研究结果表明,心脏环曲涉及管状组织内的动态和内在细胞行为,与当前基于管边界处生长和/或应力的 LR 不对称的模型提供了一个显著不同的观点。最后,我们提出了一个最小的充分模型来解释初始心脏环曲,该模型也得到了力学模拟的支持。