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Development of the epicardium and its role during regeneration

The epicardium is a unicellular epithelial layer of that envelops the myocardium. It derives from the proepicardium (PE), a group of cells that arises at the inflow tract of the forming heart. PE cells attach to the myocardium and form an epithelial covering, called the epicardium. During development, epicardial derived cells (EPDCs) delaminate from the embryonic epicardium, undergo epithelial-mesenchymal transition (EMT), and differentiate into smooth muscle and vascular endothelial cells of the coronary vasculature and into cardiac interstitial fibroblasts. An additional differentiation of EPDCs into cardiomyocytes is currently under debate. The epicardium also promotes the development of the myocardium through a paracrine action. In the adult, damage to the myocardium leads to the rapid reexpression of epicardial genes such as Wilms tumour 1 encoding gene (Wt1). Also, an early response to cardiac damage is the formation of a thickened epicardial cap over the injured area. These observations suggest a role for the epicardium as a source both of signals and of progenitor cells during cardiac regeneration.

We use the zebrafish as a model system to analyze the molecular mechanisms of epicardium formation in vivo. The zebrafish heart is also a well-established model for the study of cardiac regeneration, given its capacity to regenerate cardiac tissue after injury. We have recently described the use of cryoinjury for inducing cardiac injury in zebrafish. Heart cryoinjury induces massive cell death and the formation of a fibrotic scar, resembling the outcome of myocardial infarction in mammals. Importantly, unlike mammals, the zebrafish is able to remove these massive fibrotic heart lesions and regenerate the lost tissue, indicating the existence of endogenous mechanisms that allow the degradation of fibrotic tissue and its replacement by newly-formed cells.

Our work is aimed at understanding the morphogenesis of the epicardium and its role as a source of cells and signals during development and regeneration. A second main goal of the laboratory is to elucidate the molecular mechanisms of fibrotic tissue degradation in zebrafish.

Nadia Mercader
  • Nadia Mercader Huber
  • Junior group leader
  • Ext.3105
Nadia Mercader received her bachelor’s degree in Biology from the Swiss Federal Institute of Technology (Zurich) in 1998, and was awarded her PhD in Molecular Biology by the Universidad Autónoma de Madrid in 2003. The subject of her doctoral studies, carried out in Miguel Torres’s laboratory (CNB-CSIC), was the role of Meis genes during proximodistal vertebrate limb development. After her PhD, Nadia continued her study of the function of Meis genes during limb regeneration in urodeles. These studies were performed in Miguel Torres’s laboratory (CNB-CSIC) and in Elly Tanaka’s laboratory (Max Planck Institute of Cell Biology and Genetics, Dresden, Germany). During her postdoc with Carl Neumann at the EMBL (Heidelberg, Germany), Nadia studied early events in limb induction using zebrafish as a model organism. Nadia joined the CNIC in March 2007.