Key result
The adult mouse epicardium contains a dynamic population of CD45+ hematopoietic cells encased by extracellular matrix that responds to myocardial infarction and is replenished by bone marrow.
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The discovery of a dynamic haematopoietic cell population within the adult epicardium that responds to myocardial infarction challenges the view of the epicardium as a simple mesothelium and highlights a novel cellular target for cardiac repair.
The epicardium is a cellular source with the potential to reconstitute lost cardiovascular tissue following myocardial infarction. Here we show that the adult epicardium contains a population of CD45+ haematopoietic cells (HCs), which are located proximal to coronary vessels and encased by extracellular matrix (ECM). This complex tertiary structure is established during the regenerative window between post-natal days 1 and 7. We show that these HCs proliferate within the first 24 h and are released between days 2 and 7 after myocardial infarction. The ECM subsequently reforms to encapsulate HCs after 21 days. Vav1-tdTomato labelling reveals an integral contribution of CD45+ HCs to the developing epicardium, which is not derived from the proepicardial organ. Transplantation experiments with either whole bone marrow or a Vav1+ subpopulation of cells confirm a contribution of HCs to the intact adult epicardium, which is elevated during the first 24 weeks of adult life but depleted in aged mice. The murine epicardium forms an envelope around the heart and contains cells that can participate in cardiac repair. Here the authors discover a population of epicardial cells derived from blood cells, which proliferate and change their surrounding extracellular matrix in response to cardiac injury.
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Balmer et al. (2014) studied Myocardial infarction (preclinical model). Lineage tracing and bone marrow transplantation was evaluated on Cellular composition and hematopoietic contribution to the epicardium. The adult mouse epicardium contains a dynamic population of CD45+ hematopoietic cells encased by extracellular matrix that responds to myocardial infarction and is replenished by bone marrow.
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