Briefing

Research informs future treatments for heart failure

Publicly released:
Australia; QLD

QIMR Berghofer researchers have contributed to a new discovery, unlocking how heart muscle cells can be restored, informing the development of therapies for heart failure. Given human heart muscle cells lose their ability to regenerate shortly after birth, cardiac tissue isn’t able to regain its function after damage.

Media release

From: QIMR Berghofer Medical Research Institute

QIMR Berghofer researchers have contributed to a new discovery, unlocking how heart muscle cells can be restored, informing the development of therapies for heart failure. Given human heart muscle cells lose their ability to regenerate shortly after birth, cardiac tissue isn’t able to regain its function after damage.

Research Officer at QIMR Berghofer’s Cardiac Drug Discovery Lab, Lynn Devilée and a team of international collaborators led by Baylor College of Medicine Assistant Professor Riham Abouleisa, identified that cardiac cell restoration can be reactivated by manipulating calcium influx. However, there is a fine balance between lowering calcium influx to enable cardiac cell renewal and too little calcium influx, causing the heart to stop.

" The findings pave the way for treatments that target calcium influx to repair damaged tissue and restore healthy heart function. The challenge remains how to manipulate this process without interfering with normal heart function," said Research Officer Lynn Devilee

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Research Springer Nature, Web page Journal article
Supplementary Information Springer Nature, Web page Blog post accompanying research paper
Journal/
conference:
NPJ Regenerative Medicine
Research:Paper
Organisation/s: QIMR Berghofer Medical Research Institute, Queensland University of Technology (QUT), The University of Queensland
Funder: This research was funded by NIH grants F32HL149140 (R.R.E.A.), R01HL147921, P30GM127607, R15HL168688, R01HL166280 (T.M.A.M.), and American Heart Association grant 16SDG29950012 (T.M.A.M). J.E.H. is supported by a Snow Medical Fellowship. Ultrasound experiments were supported by the Baylor College of Medicine Mouse Metabolism and Phenotyping Core which is supported by NIH (S10OD032380, UM1HG006348, R01DK114356, R01HL130249). We would like to acknowledge Beverly Dixon for her technical support in animal care and surgeries.
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