03:41pm Saturday 18 November 2017

Mammalian Heart Regenerative Capacity Depends on Severity of Injury

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 cryoinjury – 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.

Neonatal mouse heart showing basal level of proliferating cardiomyocytes.
(Red- cardiomyocytes; Green- proliferating cardiomyocytes; RV-right ventricle; LV-left ventricle)

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.

Newborn 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 transmural injury, is associated with a blood supply blockage to the full thickness of the heart. Non-transmural 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 transmural 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.

Additional contributors include Ali Darehzereshki, Nicole Rubin, Laurent Gamba, Jieun Kim, James Fraser, Ying Huang, Joshua Billings, John Wood, The Saban Research Institute of CHLA; Robabeh Mohammadzadeh, Broad Center of Stem Cell and Regenerative Medicine, USC; Vesa Kaartinen, University of Michigan. Funding was provided in part by the National Heart, Lung and Blood Institute R01HL096121, The Saban Research Institute Career Development Award, and the California Institute of Regenerative Medicine (CIRM) postdoctoral fellowship TG2-01168.

Link to study: http://www.sciencedirect.com/science/article/pii/S0012160614006484

About Children’s Hospital Los Angeles
Children’s Hospital Los Angeles has been named the best children’s hospital on the West Coast and among the top five in the nation for clinical excellence with its selection to the prestigious U.S. News & World Report Honor Roll. Children’s Hospital is home to The Saban Research Institute, one of the largest and most productive pediatric research facilities in the United States. Children’s Hospital is also one of America’s premier teaching hospitals through its affiliation since 1932 with the Keck School of Medicine of the University of Southern California.

 

For more information, visit CHLA.org and follow us on ResearCHLAblog.org

 

 
Media contact: Jennifer Jing, jjing@chla.usc.edu

 

323-361-1812 or 323-361-6453


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