Lluri Gentian, Huang Vincent, Touma Marlin, Liu Xiaoqian, Harmon Andrew W, Nakano Atsushi
Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA; Department of Medicine, Section of Cardiology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Department of Molecular Cell and Developmental Biology, University of California, Los Angeles, Los Angeles, CA 90095, USA.
J Mol Cell Cardiol. 2015 Sep;86:199-207. doi: 10.1016/j.yjmcc.2015.07.021. Epub 2015 Aug 1.
During embryogenesis, hematopoietic cells appear in the myocardium prior to the initiation of coronary formation. However, their role is unknown.
Here we investigate whether pre-existing hematopoietic cells are required for the formation of coronary vasculature.
As a model of for hematopoietic cell deficient animals, we used Runx1 knockout embryos and Vav1-cre; R26-DTA embryos, latter of which genetically ablates 2/3 of CD45(+) hematopoietic cells. Both Runx1 knockout embryos and Vav1-cre; R26-DTA embryos revealed disorganized, hypoplastic microvasculature of coronary vessels on section and whole-mount stainings. Furthermore, coronary explant experiments showed that the mouse heart explants from Runx1 and Vav1-cre; R26-DTA embryos exhibited impaired coronary formation ex vivo. Interestingly, in both models it appears that epicardial to mesenchymal transition is adversely affected in the absence of hematopoietic progenitors.
Hematopoietic cells are not merely passively transported via coronary vessel, but substantially involved in the induction of the coronary growth. Our findings suggest a novel mechanism of coronary growth.
在胚胎发生过程中,造血细胞在冠状动脉形成之前就出现在心肌中。然而,它们的作用尚不清楚。
在此我们研究冠状动脉脉管系统的形成是否需要预先存在的造血细胞。
作为造血细胞缺陷动物模型,我们使用了Runx1基因敲除胚胎和Vav1-cre; R26-DTA胚胎,后者通过基因手段消除了2/3的CD45(+)造血细胞。Runx1基因敲除胚胎和Vav1-cre; R26-DTA胚胎在切片和整体染色上均显示冠状动脉的微血管系统紊乱且发育不全。此外,冠状动脉外植体实验表明,来自Runx1和Vav1-cre; R26-DTA胚胎的小鼠心脏外植体在体外冠状动脉形成受损。有趣的是,在这两种模型中,在缺乏造血祖细胞的情况下,心外膜向间充质转变似乎受到不利影响。
造血细胞不仅仅是通过冠状动脉被动运输,而是在很大程度上参与冠状动脉生长的诱导。我们的发现提示了一种冠状动脉生长的新机制。