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Ultrastructural and kinetic evidence support that thick filaments slide through the Z-disc.

André TomalkaMaximilian HeimAnnika KlotzChristian RodeTobias Siebert
Published in: Journal of the Royal Society, Interface (2022)
How myofilaments operate at short mammalian skeletal muscle lengths is unknown. A common assumption is that thick (myosin-containing) filaments get compressed at the Z-disc. We provide ultrastructural evidence of sarcomeres contracting down to 0.44 µm-approximately a quarter of thick filament resting length-in long-lasting contractions while apparently keeping a regular, parallel thick filament arrangement. Sarcomeres produced force at such extremely short lengths. Furthermore, sarcomeres adopted a bimodal length distribution with both modes below lengths where sarcomeres are expected to generate force in classic force-length measurements. Mammalian fibres did not restore resting length but remained short after deactivation, as previously reported for amphibian fibres, and showed increased forces during passive re-elongation. These findings are incompatible with viscoelastic thick filament compression but agree with predictions of a model incorporating thick filament sliding through the Z-disc. This more coherent picture of mechanical mammalian skeletal fibre functioning opens new perspectives on muscle physiology.
Keyphrases
  • skeletal muscle
  • single molecule
  • heart rate
  • heart rate variability
  • insulin resistance
  • adipose tissue
  • metabolic syndrome
  • atomic force microscopy
  • high speed