Ishii Yasuo, Langberg Jonathan D, Hurtado Romulo, Lee Sharrell, Mikawa Takashi
University of California San Francisco, Cardiovascular Research Institute, Box 2711, Rock Hall Room 384D, 1550 4th Street, San Francisco, CA 94158-2324, USA.
Development. 2007 Oct;134(20):3627-37. doi: 10.1242/dev.005280. Epub 2007 Sep 12.
Cells of the coronary vessels arise from a unique extracardiac mesothelial cell population, the proepicardium, which develops posterior to the sinoatrial region of the looping-stage heart. Although contribution of the proepicardial cells to cardiac development has been studied extensively, it remains unresolved how the proepicardium is induced and specified in the mesoderm during embryogenesis. It is known, however, that the proepicardium develops from the mesothelium that overlays the liver bud. Here, we show that the expression of proepicardial marker genes - Wt1, capsulin (epicardin, pod1, Tcf21) and Tbx18, can be induced in naïve mesothelial cells by the liver bud, both in vitro and in vivo. Lateral embryonic explants, when co-cultured with the liver bud, were induced to express these proepicardial marker genes. The same induction of the marker genes was detected in vivo when a quail liver bud was implanted in the posterior-lateral regions of a chick embryo. This ectopic induction of marker gene expression was not evident when other endodermal tissues, such as the lung bud or stomach, were implanted. This inductive response to the liver bud was not detectable in host embryos before stage 12 (16-somite stage). These results suggest that, after a specific developmental stage, a large area of the mesothelium becomes competent to express proepicardial marker genes in response to localized liver-derived signal(s). The developmentally regulated competency of mesothelium and a localized inductive signal might play a role in restricting the induction of the proepicardial marker gene expression to a specific region of the mesothelium. The data might also provide a foundation for future engineering of a coronary vascular progenitor population.
冠状血管的细胞起源于一个独特的心脏外间皮细胞群,即心外膜原基,它在心脏环化期心脏的窦房区域后方发育。尽管心外膜原基细胞对心脏发育的贡献已得到广泛研究,但在胚胎发生过程中,心外膜原基如何在中胚层中被诱导和特化仍未得到解决。然而,已知心外膜原基是从覆盖肝芽的间皮发育而来的。在此,我们表明,心外膜标记基因——Wt1、荚膜蛋白(心外膜蛋白、足盘蛋白1、Tcf21)和Tbx18的表达,在体外和体内均可由肝芽在幼稚间皮细胞中诱导产生。当外侧胚胎外植体与肝芽共培养时,可诱导其表达这些心外膜标记基因。当将鹌鹑肝芽植入鸡胚的后外侧区域时,在体内也检测到了标记基因的相同诱导情况。当植入其他内胚层组织,如肺芽或胃时,标记基因的这种异位诱导并不明显。在12期(16体节期)之前的宿主胚胎中未检测到对肝芽的这种诱导反应。这些结果表明,在特定的发育阶段之后,大面积的间皮能够响应局部肝源性信号而表达心外膜标记基因。间皮的发育调控能力和局部诱导信号可能在将心外膜标记基因表达的诱导限制在间皮的特定区域中发挥作用。这些数据也可能为未来构建冠状血管祖细胞群提供基础。