Pérez-Pomares J M, Phelps A, Sedmerova M, Carmona R, González-Iriarte M, Muñoz-Chápuli R, Wessels A
Department of Cell Biology and Anatomy, Medical University of South Carolina, Charleston, South Carolina, 29425, USA.
Dev Biol. 2002 Jul 15;247(2):307-26. doi: 10.1006/dbio.2002.0706.
Epicardially derived cells (EPDCs) delaminate from the primitive epicardium through an epithelial-to-mesenchymal transformation (EMT). After this transformation, a subpopulation of cells progressively invades myocardial and valvuloseptal tissues. The first aim of the study was to determine the tissue-specific distribution of two molecules that are thought to play a crucial function in the interaction between EPDCs and other cardiac tissues, namely the Wilms' Tumor transcription factor (WT1) and retinaldehyde-dehydrogenase2 (RALDH2). This study was performed in normal avian and in quail-to-chick chimeric embryos. It was found that EPDCs that maintain the expression of WT1 and RALDH2 initially populate the subepicardial space and subsequently invade the ventricular myocardium. As EPDCs differentiate into the smooth muscle and endothelial cell lineage of the coronary vessels, the expression of WT1 and RALDH2 becomes downregulated. This process is accompanied by the upregulation of lineage-specific markers. We also observed EPDCs that continued to express WT1 (but very little RALDH2) which did not contribute to the formation of the coronary system. A subset of these cells eventually migrates into the atrioventricular (AV) cushions, at which point they no longer express WT1. The WT1/RALDH2-negative EPDCs in the AV cushions do, however, express the smooth muscle cell marker caldesmon. The second aim of this study was to determine the impact of abnormal epicardial growth on cardiac development. Experimental delay of epicardial growth distorted normal epicardial development, reduced the number of invasive WT1/RALDH2-positive EPDCs, and provoked anomalies in the coronary vessels, the ventricular myocardium, and the AV cushions. We suggest that the proper development of ventricular myocardium is dependent on the invasion of undifferentiated, WT1-positive, retinoic acid-synthesizing EPDCs. Furthermore, we propose that an interaction between EPDCs and endocardial (derived) cells is imperative for correct development of the AV cushions.
心外膜来源细胞(EPDCs)通过上皮-间充质转化(EMT)从原始心外膜分层。这种转化后,一部分细胞逐渐侵入心肌和瓣膜间隔组织。该研究的首要目的是确定两种分子在EPDCs与其他心脏组织相互作用中所起关键作用的组织特异性分布,这两种分子即威尔姆斯瘤转录因子(WT1)和视黄醛脱氢酶2(RALDH2)。这项研究在正常禽类和鹌鹑-鸡嵌合胚胎中进行。研究发现,维持WT1和RALDH2表达的EPDCs最初填充心外膜下间隙,随后侵入心室心肌。随着EPDCs分化为冠状血管的平滑肌和内皮细胞谱系,WT1和RALDH2的表达下调。这一过程伴随着谱系特异性标志物的上调。我们还观察到持续表达WT1(但RALDH2表达很少)的EPDCs,它们对冠状系统的形成没有贡献。这些细胞中的一部分最终迁移到房室(AV)垫,此时它们不再表达WT1。然而,AV垫中WT1/RALDH2阴性的EPDCs确实表达平滑肌细胞标志物钙调蛋白。该研究的第二个目的是确定心外膜异常生长对心脏发育的影响。心外膜生长的实验性延迟扭曲了正常的心外膜发育,减少了侵入性WT1/RALDH2阳性EPDCs的数量,并引发了冠状血管、心室心肌和AV垫的异常。我们认为心室心肌的正常发育依赖于未分化的、WT1阳性、视黄酸合成的EPDCs的侵入。此外,我们提出EPDCs与心内膜(衍生)细胞之间的相互作用对于AV垫的正确发育至关重要。