4.5 Article

Sarcomere length measurement reliability in single myofibrils

Journal

JOURNAL OF BIOMECHANICS
Volume 126, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.jbiomech.2021.110628

Keywords

Muscle; Sarcomere; Length Non-Uniformity; Myofibril; Measurements; Titin; Residual force enhancement; Stability; Residual force depression; Force-length relationship

Funding

  1. Natural Sciences and Engineering Research Council of Canada
  2. Canadian Institutes of Health Research through the Canada Research Chair Programme
  3. Killam Foun-dation

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Sarcomere length non-uniformities in skeletal muscles are associated with important mechanical properties and can be used to explain muscle properties and contractile mechanisms. However, measurements obtained with light microscopy may contain noise, and the impact of intensity threshold choice on the results should be considered.
Sarcomere length non-uniformities occur at all structural levels of skeletal muscles and have been associated with important mechanical properties. Changes in sarcomere length non-uniformities in the nano- and sub-nanometer range have been used to explain muscle properties and contractile mechanisms. Typically, these measurements rely on light microscopy with a limited spatial resolution. One critical aspect in sarcomere length determination is the relatively arbitrary choice of intensity thresholds used to delineate sarcomere structures, such as A-bands or Z-lines. In experiments, these structures are typically distorted, intensity profiles vary, and baselines drift, resulting in asymmetric intensity patterns, causing changes in the centroid location of these structures depending on threshold choice, resulting in changes of sarcomere lengths. The purpose of this study was to determine the changes in (half-) sarcomere lengths associated with small changes in the A-band threshold choice. Sarcomere and half-sarcomere length changes for minute variations in A-band threshold were 28 nm (+/- 28 nm) and 18 nm (+/- 22 nm), respectively, and for the entire feasible range of thresholds across A-bands were 123 nm (+/- 88 nm) and 99 nm (+/- 105 nm), respectively. We conclude from these results that (half-) sarcomere lengths in the nanometer range obtained with light microcopy are noise, and the functional implications associated with such data should be discarded. We suggest that a functional resolution for sarcomere length of 100 nm (0.1 mu m) is reasonable and 50 nm (0.05 mu m) might be possible under ideal conditions.

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