Overcoming cardiac pacemaker “source-sink mismatch”

Instead of complication-prone electronic cardiac pacemakers, biomedical engineers at Georgia Tech and Emory envision the creation of “biological pacemakers.” Hee Cheol Cho and colleagues have been taking advantage of his work on a gene called TBX18 that can reprogram heart muscle cells into specialized pacemaker cells.

Graduate student Sandra Grijalva in lab

Every heartbeat originates from a small group of cells in the heart called the sinoatrial node. How these cells drive contractions in the relatively massive, and electrically sturdy, rest of the heart is a problem cardiology researchers call the “source-sink mismatch.” Until Cho’s innovations, it was only possible to isolate a handful of pacemaker cells from animal hearts, and the isolated cells could not be cultured.

Cho and colleagues recently published a paper in Advanced Science describing TBX18-induced pacemaker cell spheroids, a platform for studying source-sink mismatch in culture

Graduate student Sandra Grijalva is the first author of the paper. We first spotted Grijalva’s work when it was presented at the American Heart Association meeting in 2017. She and Cho are part of the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory, and the Emory-Children’s-GT Pediatric Research Alliance.

Cho’s work with Phil Santangelo on a messenger RNA-based approach to creating more pacemaker cells in situ was highlighted by Georgia Tech and by Emory’s Office of Technology Transfer, which gave them an “Innovation of the Year” award for 2018. Also in September 2019, Cho’s lab published a paper in Experimental and Molecular Medicine on the hardiness of TBX18-induced pacemaker cells. They are more resistant to metabolic and hypoxic stress, possibly because of smaller and fewer mitochondria, the researchers report.

Posted on by Quinn Eastman in Heart Leave a comment

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Quinn Eastman

Science Writer, Research Communications qeastma@emory.edu 404-727-7829 Office

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