Heart attacks are damaging, and the severity depends on how long blood flow has been interrupted; when temporarily deprived of oxygen, heart cells die. In addition, the heart can’t rebuild its tissue, leading to its failure, the main cause of mortality and morbidity worldwide.
Image credit: Macro Mama via stocksnap.io, CCO Public Domain
Unlike humans and other mammals, however, adult zebrafish can regenerate damaged heart tissue. In a new study, Université de Montréal professor Ruben Marin Juez, a recruit at the CHU Sainte-Justine Research Centre, reveals the complex mechanisms that allow this marine animal to “repair its heart” after injury.
Juez’s discovery offers a promising perspective on the therapeutic avenues of cardiac revascularization and regeneration in humans. The results are published in the journal Circulation Research.
The coronary vessels transport blood. However, in adult zebrafish, they are also essential for heart muscle cell proliferation and healing. It is the injury itself that would immediately trigger a regenerative response from the coronary vessel cells, which is needed to reconstitute the tissue.
Identifying molecules and cell signaling
In their new study, Juez’s international research team focused on identifying and plotting the interaction of molecules that allow this regenerative response. The scientists studied the cell signaling that generates coronary vessel cell proliferation.
By manipulating the action and expression of these molecules, they were able to identify two proteins – Emilin2a and Cxcl8a – as key players in the revascularization and regeneration of cardiac tissue.
“We already knew that, after cardiac injury, vascular endothelial growth factor C (Vegf-C) was upregulated in adult zebrafish and that this factor was involved in cardiac regeneration,” said Juez.
“However, we discovered that Vegf-C signaling promotes the expression of Emilin2a, which, in turn, fosters the expression of Cxcl8a. We also discovered that manipulation of Emilin2a protein expression alone can modulate the regenerative response of cardiac muscle cells.
“This discovery will make it possible to study the potential of this molecule for treatment purposes in people with heart damage.”
Source: University of Montreal