No. 5/February 15, 2007
Targeting Myocardial Disease
The Muscle Protein Titin Regulates the Contractile Properties of the Heart
Mutations of
titin, the largest protein in humans, can lead to myopathies and heart disease.
Titin is an important component of the smallest mechanical unit of the heart
muscle, the sarcomere. There, titin functions as a molecular spring and ensures
that the heart muscle efficiently fills with blood – an important prerequisite
that sufficient blood is pumped through the body with every heartbeat, when
sarcomeres contract.
Now, for
the first time Professor
These findings, which have just been published in the American journal Circulation* (DOI:10.1161/CIRCULATIONAHA.106.645499), may explain why people with a mutant (non-functional) form of titin develop heart disease. The researchers hope their findings will contribute to the development of causal therapies for myocardial diseases.
Cardiac Hypertrophy and Reduced
Contractility in Hearts Deficient in the Titin Kinase Region Jun Peng, Katy Raddatz, Jeffrey D.
Molkentin, Yiming Wu, Siegfried Labeit, Henk Granzier and Michael Gotthardt Department of Veterinary and Comparative Anatomy, Pharmacology, and
Physiology, Washington State University, Pullman (J.P, Y.W., H.G., M.G.);
Neuromuscular and Cardiovascular Cell Biology, Max-Delbrück Center for Molecular
Medicine, Berlin, Germany (K.R., M.G.); Division of Molecular Cardiovascular
Biology, Department of Pediatrics, Children’s Hospital Medical Center,
Cincinnati, Ohio (J.M.); and Department of Anesthesiology, Mannheim University,
Mannheim, Germany (S.L.).
Barbara Bachtler
Press and Public Affairs
Max Delbrück Center for Molecular Medicine (MDC) Berlin-Buch
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Germany
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