Kokkinopoulos Ioannis, Ishida Hidekazu, Saba Rie, Ruchaya Prashant, Cabrera Claudia, Struebig Monika, Barnes Michael, Terry Anna, Kaneko Masahiro, Shintani Yasunori, Coppen Steven, Shiratori Hidetaka, Ameen Torath, Mein Charles, Hamada Hiroshi, Suzuki Ken, Yashiro Kenta
Translational Medicine and Therapeutics, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Translational Medicine and Therapeutics, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; Physiology and Pathology, University of São Paulo State - UNESP, Araraquara School of Dentistry, Araraquara, São Paulo, Brazil.
PLoS One. 2015 Oct 15;10(10):e0140831. doi: 10.1371/journal.pone.0140831. eCollection 2015.
In the early vertebrate embryo, cardiac progenitor/precursor cells (CPs) give rise to cardiac structures. Better understanding their biological character is critical to understand the heart development and to apply CPs for the clinical arena. However, our knowledge remains incomplete. With the use of single-cell expression profiling, we have now revealed rapid and dynamic changes in gene expression profiles of the embryonic CPs during the early phase after their segregation from the cardiac mesoderm. Progressively, the nascent mesodermal gene Mesp1 terminated, and Nkx2-5+/Tbx5+ population rapidly replaced the Tbx5low+ population as the expression of the cardiac genes Tbx5 and Nkx2-5 increased. At the Early Headfold stage, Tbx5-expressing CPs gradually showed a unique molecular signature with signs of cardiomyocyte differentiation. Lineage-tracing revealed a developmentally distinct characteristic of this population. They underwent progressive differentiation only towards the cardiomyocyte lineage corresponding to the first heart field rather than being maintained as a progenitor pool. More importantly, Tbx5 likely plays an important role in a transcriptional network to regulate the distinct character of the FHF via a positive feedback loop to activate the robust expression of Tbx5 in CPs. These data expands our knowledge on the behavior of CPs during the early phase of cardiac development, subsequently providing a platform for further study.
在早期脊椎动物胚胎中,心脏祖细胞/前体细胞(CPs)产生心脏结构。更好地了解它们的生物学特性对于理解心脏发育以及将CPs应用于临床领域至关重要。然而,我们的知识仍然不完整。通过使用单细胞表达谱分析,我们现在揭示了胚胎CPs从心脏中胚层分离后的早期阶段基因表达谱的快速动态变化。逐渐地,新生中胚层基因Mesp1终止,随着心脏基因Tbx5和Nkx2-5表达的增加,Nkx2-5+/Tbx5+群体迅速取代了Tbx5low+群体。在早期头褶阶段,表达Tbx5的CPs逐渐显示出具有心肌细胞分化迹象的独特分子特征。谱系追踪揭示了该群体在发育上的独特特征。它们仅朝着对应于第一心脏区域的心肌细胞谱系进行渐进性分化,而不是作为祖细胞池维持。更重要的是,Tbx5可能在转录网络中发挥重要作用,通过正反馈回路调节第一心脏区域(FHF)的独特特征,以激活CPs中Tbx5的强劲表达。这些数据扩展了我们对心脏发育早期阶段CPs行为的认识,随后为进一步研究提供了一个平台。