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The sinus venosus progenitors separate and diversify from the first and second heart fields early in development.

机译:静脉窦祖细胞在发育早期与第一和第二心脏区域分开并多样化。

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AIMS: During development, the heart tube grows by differentiation of Isl1(+)/Nkx2-5(+) progenitors to the arterial and venous pole and dorsal mesocardium. However, after the establishment of the heart tube, Tbx18(+) progenitors were proposed to form the Tbx18(+)/Nkx2-5(-) sinus venosus and proepicardium. To elucidate the relationship between these contributions, we investigated the origin of the Tbx18(+) sinus venosus progenitor population in the cardiogenic mesoderm and its spatial and temporal relation to the second heart field during murine heart development. METHODS AND RESULTS: Explant culture revealed that the Tbx18(+) cell population has the potential to form Nkx2-5(-) sinus venosus myocardium. Three-dimensional reconstruction of expression patterns showed that during heart tube elongation, the Tbx18(+) progenitors remained spatially and temporally separate from the Isl1(+) second heart field, only overlapping with the Isl1(+) domain at the right lateral side of the inflow tract, where the sinus node developed. Consistently, genetic lineage analysis revealed that the Tbx18(+) descendants formed the sinus venosus myocardium, but did not contribute to the pulmonary vein myocardium that developed in the Isl1(+) second heart field. By means of DiI labelling and expression analysis, the origin of the sinus venosus progenitor population was traced to the lateral rim of splanchnic mesoderm that down-regulated Nkx2-5 expression approximately 2 days before its differentiation into sinus venosus myocardium. CONCLUSION: Our data indicate that the cardiogenic mesoderm contains an additional progenitor subpopulation that contributes to the sinus venosus myocardium. After patterning of the cardiogenic mesoderm, this progenitor population remains spatially separated and genetically distinctive from the second heart field subpopulation.
机译:目的:在发育过程中,Isl1(+)/ Nkx2-5(+)祖细胞分化为动脉和静脉极以及背中膜,从而使心管生长。但是,在建立心管后,提出了Tbx18(+)祖细胞形成Tbx18(+)/ Nkx2-5(-)静脉窦和前皮膜。为了阐明这些贡献之间的关系,我们调查了心源性中胚层中Tbx18(+)静脉窦祖细胞的起源及其在鼠心脏发育过程中与第二心脏场的时空关系。方法和结果:外植体培养表明,Tbx18(+)细胞群具有形成Nkx2-5(-)静脉窦窦心肌的潜力。表达模式的三维重建显示,在心管伸长过程中,Tbx18(+)祖细胞在空间和时间上与Isl1(+)第二心脏场保持分离,仅与Isl1(+)结构域在右侧右侧重叠鼻窦结所在的流入通道。一致地,遗传谱系分析表明Tbx18(+)后代形成了静脉窦窦心肌,但对在Isl1(+)第二心脏场中发育的肺静脉心肌没有贡献。通过DiI标记和表达分析,窦静脉祖细胞群的起源可追溯到内脏中胚层的外侧边缘,该内脏中胚层在Nkx2-5表达分化为窦静脉心肌之前约2天下调了其表达。结论:我们的数据表明,心源性中胚层包含一个额外的祖细胞亚群,有助于窦静脉心肌。在将心源性中胚层图案化后,该祖细胞群在空间上是分离的,并且在遗传上与第二心脏区域亚群不同。

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