Division of Biomedical Sciences, St George's University of London, Cranmer Terrace, London SW17 0RE, United Kingdom.
Circ Res. 2012 Oct 26;111(10):1323-35. doi: 10.1161/CIRCRESAHA.112.271247. Epub 2012 Sep 5.
The second heart field (SHF) contains progenitors of all heart chambers, excluding the left ventricle. The SHF is patterned, and the anterior region is known to be destined to form the outflow tract and right ventricle.
The aim of this study was to map the fate of the posterior SHF (pSHF).
We examined the contribution of pSHF cells, labeled by lipophilic dye at the 4- to 6-somite stage, to regions of the heart at 20 to 25 somites, using mouse embryo culture. Cells more cranial in the pSHF contribute to the atrioventricular canal (AVC) and atria, whereas those more caudal generate the sinus venosus, but there is intermixing of fate throughout the pSHF. Caudal pSHF contributes symmetrically to the sinus venosus, but the fate of cranial pSHF is left/right asymmetrical. Left pSHF moves to dorsal left atrium and superior AVC, whereas right pSHF contributes to right atrium, ventral left atrium, and inferior AVC. Retrospective clonal analysis shows the relationships between AVC and atria to be clonal and that right and left progenitors diverge before first and second heart lineage separation. Cranial pSHF cells also contribute to the outflow tract: proximal and distal at 4 somites, and distal only at 6 somites. All outflow tract-destined cells are intermingled with those that will contribute to inflow and AVC.
These observations show asymmetric fate of the pSHF, resulting in unexpected left/right contributions to both poles of the heart and can be integrated into a model of the morphogenetic movement of cells during cardiac looping.
第二心区(SHF)包含所有心腔的祖细胞,不包括左心室。SHF 是有图案的,已知其前区将形成流出道和右心室。
本研究旨在绘制后 SHF(pSHF)的命运图。
我们通过胚胎培养检查了在 4-6 体节阶段用亲脂性染料标记的 pSHF 细胞对 20-25 体节心脏区域的贡献。pSHF 中颅侧的细胞有助于房室管(AVC)和心房,而那些颅侧的细胞产生窦房结,但在整个 pSHF 中存在命运的混合。尾侧 pSHF 对称地有助于窦房结,但颅侧 pSHF 的命运是左右不对称的。左 pSHF 移至背侧左心房和上 AVC,而右 pSHF 则有助于右心房、腹侧左心房和下 AVC。回溯性克隆分析显示 AVC 和心房之间的关系是克隆的,并且右和左祖细胞在第一和第二心前体分离之前就已经分化。颅侧 pSHF 细胞也有助于流出道:在 4 个体节时为近端和远端,在 6 个体节时仅为远端。所有流出道定向的细胞都与那些将有助于流入和 AVC 的细胞混合在一起。
这些观察结果表明 pSHF 的命运是不对称的,导致对心脏两极的意外的左右贡献,并且可以整合到心脏环曲过程中细胞形态发生运动的模型中。