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Updated: Jun 5, 2026

Assessment of Myofilament Ca2+ Sensitivity Underlying Cardiac Excitation-contraction Coupling
Published on: August 1, 2016
Reiji Natori, Setsuro Ebashi, and excitation-contraction coupling
1Pharmacology, Saitama Medical University, 21-7 Wakita-honcho, Kawagoe, Saitama, Japan. makoendo@saitama-med.ac.jp
Abstract:
The achievements of Natori and Ebashi, which greatly contributed to the progress in studies of excitation-contraction coupling, were reviewed. Natori succeeded in removing the cell membrane of an isolated fiber of skeletal muscle to prepare a skinned fiber, which still responded to an electrical stimulation with propagated contraction. Skinned fibers showed elastic extensibility beyond the elastic limit of intact muscle fibers. Based on this elasticity Natori predicted the presence of an elastic components, later found as connectin. Skinned fibers, an excellent experimental system, contributed greatly to the progress in subsequent studies. Ebashi showed that the essential principle of the relaxing factor was not the ATP-regenerating enzymes as generally thought, but a particulate fraction with MgATPase. Then he clearly showed that a minute amount of Ca(2+) is necessary for the contractile reaction of actomyosin, and that the relaxing factor strongly accumulates Ca(2+) in the presence of ATP and causes relaxation by the removal of Ca(2+). He further discovered that the Ca(2+)-induced regulation of the contractile reaction of the myosin-actin system requires the presence of tropomyosin and a new protein, troponin. Troponin binds to a specific site on tropomyosin, which in turn binds to actin in the thin filament. Troponin is the Ca(2+)-receptive protein, and changes in troponin molecules upon Ca(2+) binding is transmitted to actin through tropomyosin to regulate the actin-myosin interaction. Through these findings, the excitation was connected by Ca(2+) with the contraction.
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