4.7 Article

The mechanical behavior of individual sarcomeres of myofibrils isolated from rabbit psoas muscle

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 297, Issue 5, Pages C1211-C1219

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00233.2009

Keywords

cross-bridges; force-length relation; myosin-actin interaction

Funding

  1. Canadian Institutes of Health Research

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Pavlov I, Novinger R, Rassier DE. The mechanical behavior of individual sarcomeres of myofibrils isolated from rabbit psoas muscle. Am J Physiol Cell Physiol 297: C1211-C1219, 2009. First published August 26, 2009; doi:10.1152/ajpcell.00233.2009.-The goal of this study was to develop a system to experiment with sarcomeres mechanically isolated from skeletal muscles. Single myofibrils from rabbit psoas were transferred into a temperature-controlled (22 degrees C or 15 degrees C) experimental chamber, and sarcomeres were isolated using precalibrated glass microneedles that were pierced externally, adjacent to the Z-lines. The force produced during activation was measured by tracking the displacement of the microneedles, and the sarcomere and half-sarcomere changes were measured by continuously tracking the Z-lines and A-bands position during the experiments. Sarcomeres produced a stress (force/cross-sectional area) of 112.75 +/- 4.96 nN/mu m(2) (15 degrees C) and 128.47 +/- 5.58 nN/mu m(2) (22 degrees C) at lengths between 2.0 mu m and 2.4 mu m. The descending limb was fitted with linear regression for length between 2.4 mu m and 3.5 mu m, which provided an abscissa extrapolating to 3.87 mu m. The force-length relation was remarkably similar to a theoretical curve based on the degree of filament overlap. During sarcomere activation, we tracked the distance between the center of the A-band and the Z-lines. At lengths below 1.6 mu m, movements of A-band were not detected. A-band movements increased with length to achieve a maximum displacement of 59.40 +/- 10.1 nm from the center at 2.0 mu m-2.4 mu m. A-band displacement decreased linearly in sarcomere lengths between 2.6 mu m and 3.6 mu m. A technique for monitoring force and length in single sarcomeres isolated from myofibrils represents a reliable technique to evaluate contractile mechanisms at the most basic, intact level of muscle organization, opening the possibility to clarify long-standing issues in the field of muscle contraction.

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