中胚层
生物
原肠化
细胞生物学
命运图
形态发生
内胚层
解剖
侧板中胚层
心脏发育
胚胎
祖细胞
胚胎发生
干细胞
胚胎干细胞
遗传学
基因
作者
Martin H. Dominguez,Alexis Leigh Krup,Jonathon M. Muncie,Benoit G. Bruneau
出处
期刊:Cell
[Elsevier]
日期:2023-02-01
卷期号:186 (3): 479-496.e23
被引量:28
标识
DOI:10.1016/j.cell.2023.01.001
摘要
Using four-dimensional whole-embryo light sheet imaging with improved and accessible computational tools, we longitudinally reconstruct early murine cardiac development at single-cell resolution. Nascent mesoderm progenitors form opposing density and motility gradients, converting the temporal birth sequence of gastrulation into a spatial anterolateral-to-posteromedial arrangement. Migrating precardiac mesoderm does not strictly preserve cellular neighbor relationships, and spatial patterns only become solidified as the cardiac crescent emerges. Progenitors undergo a mesenchymal-to-epithelial transition, with a first heart field (FHF) ridge apposing a motile juxta-cardiac field (JCF). Anchored along the ridge, the FHF epithelium rotates the JCF forward to form the initial heart tube, along with push-pull morphodynamics of the second heart field. In Mesp1 mutants that fail to make a cardiac crescent, mesoderm remains highly motile but directionally incoherent, resulting in density gradient inversion. Our practicable live embryo imaging approach defines spatial origins and behaviors of cardiac progenitors and identifies their unanticipated morphological transitions.
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