Mammalian Heart Regenerative Capacity Depends on Severity of Injury

Full recovery and normal function restored in mouse models following mild injury

Friday, 23 January 2015

This is a neonatal mouse heart showing basal

level of proliferating cardiomyocytes. (Red-

cardiomyocytes; Green- proliferating

cardiomyocytes; RV-right ventricle; LV-left

ventricle.) Credit: The Saban Research Institute

of Children's Hospital Los Angeles. 

A new study by researchers at Children's Hospital Los Angeles has shown that neonatal mouse hearts have varying regenerative capacities depending upon the severity of injury. Using cryo-injury - damaging the heart through exposure to extreme cold in order to mimic cellular injury caused by myocardial infarction - investigators found that neonatal mouse hearts can fully recover normal function following a mild injury, though fail to regenerate after a severe injury.

Published online by the journal Developmental Biology, the study suggests that cardiac regeneration strategies should be based on the type and severity of heart injury.

"Using models such as zebrafish and neonatal mice that regenerate their hearts naturally, we can begin to identify important molecules that enhance heart repair," said Ellen Lien, PhD, of The Saban Research Institute of Children's Hospital Los Angeles. Lien, who was senior author on the paper, is also an assistant professor at the Keck School of Medicine of the University of Southern California.

New born mice have shown the capacity for heart regeneration, but it is rapidly lost by seven days after birth. Approaches to extend this regenerative capacity in a mammalian model, from the neonatal period to the juvenile or adult period, could help identify new treatment options for humans.

Acute myocardial infarction, commonly known as a heart attack, can be classified according to the extent of damage to the heart muscle. Severe, or trans-mural injury, is associated with a blood supply blockage to the full thickness of the heart. Non-trans-mural injury indicates a blockage that penetrates only partially through the heart muscle. The investigators were able to develop models for both types of injury.

In addition to differences in regenerative capacity, the investigators also found an indicator of tissue fibrosis or "scarring", profibrotic marker PAI-1, was markedly elevated only after trans-mural injury. In both models post-injury, the cells that form heart muscle, cardiomyocytes, did not increase significantly. However, responses to cardiac injury repair in the outer layer of the heart (epicardium) and blood vessels (revascularization) - were present.

"If we can figure out how to activate this youthful type of myocardial regeneration program in humans, it will be a major clinical breakthrough," said David Warburton, OBE, DSc, MD, director of Developmental Biology and Regenerative Medicine at The Saban Research Institute of CHLA. Warburton is also a professor at the Keck School of Medicine of USC and was co-author on the paper.

Source: Children's Hospital Los Angeles

Contact: Jennifer Jing

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ZenMaster

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