The protein is known technically by the unusual acronym MuRF1, or muscle-specific RING finger 1, and helps regulate cardiac cellular molecules involved in abnormal enlargement of the heart. This condition, known medically as cardiac hypertrophy, occurs in 50 percent to 60 percent of people older than age 70 and makes them more prone to developing a potentially fatal type of heart failure.
"People who develop cardiac hypertrophy are prone to diastolic heart failure. Their hearts contract normally but the thickened heart muscle can't keep the blood out of the lungs," said Dr. Cam Patterson, the study's senior author. Patterson is Henry A. Foscue distinguished professor of medicine and cardiology, and professor of pharmacology and cell and developmental biology at UNC. He also directs the Carolina Cardiovascular Biology Center.
In a report published in the Proceedings of the National Academy of Sciences on Dec. 28, Patterson and co-authors said MuRF1 was responsible for signaling other molecules in heart cells to degrade another protein called troponin-1, a key player in heart muscle activity.
"Troponin-1 is a critical component of the cardiac contractile machinery," Patterson said. "It's part of the cardiac muscle cell that makes heart muscle beat."
When heart cells hypertrophy, or become enlarged, troponin-1 and other contractile proteins greatly increase in abundance, Patterson said. "And so one of the critical ways that MuRF1 reverses hypertrophy is by degrading proteins such as troponin-1."
Thus, the action of MuRF1 appears to determine the balance between hypertrophic (enlargement) and anti-hypertrophic signals in heart muscle cells, Patterson added. "This is really a fundamen
Contact: L.H. Lang
University of North Carolina School of Medicine