February 16, 2010
Protein Identified That Helps Heart Muscle Contract
UCSF researchers have discovered that a protein called B1N1 is necessary for the heart to contract. The findings, published in the Feb. 16 issue of the open access journal PLoS Biology, shed light not only on what makes a heart beat but also on heart failure, a disease where cardiac cells are no longer able to contract and pump blood through the body.
"In all of us, a heart beat occurs about once every second. For each successful heart beat, millions of individual heart muscle cells perform their own microscopic contractions, so the biology of normal heart function is based on the workings of individual heart cells. There is now less mystery to how each heart cell organizes itself to contract," said Robin Shaw, MD, PhD, an author of the study and a cardiologist in UCSF's Heart Failure and Transplantation Service.
Ting-Ting Hong, MD, PhD, lead author and postdoctoral fellow in the Shaw Laboratory at UCSF, had a mental image of calcium channels being carried on highways (known as microtubules) directly to membrane docking stations in the T-tubules. Hong confirmed her hypothesis of directed delivery of the channels and identified the protein docking station as BIN1. The study involved human heart cells and non-muscle cells that allowed researchers to recreate the delivery process using only the highways, channels and docking station. When the team mutated the docking station (BIN1), they confirmed that, like in heart failure, the cascade of signaling events necessary for heart contraction become dysfunctional.
Understanding how the heart cell organizes itself paves the way for investigators to understand what happens to the heart during heart failure.
"As we learn how healthy heart cells work, we develop a roadmap for understanding the changes that occur during heart failure," said Hong. "Now that we know about normal heart function, we can ask specific questions about what changes when disease occurs."
The goal of the research is to reverse the changes, and lessen the mortality associated with heart disease.
Funding: This work is funded by the National Institutes of Health grant HL094414. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests statement: The authors declare that no competing interests exist.
Citation: Hong T-T, Smyth JW, Gao D, Chu KY, Vogan JM, et al. (2010) BIN1 Localizes the L-Type Calcium Channel to Cardiac T-Tubules. PLoS Biol 8(2): e1000312. doi:10.1371/journal.pbio.1000312
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