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

J R Soc Interface. 2022 Dec;19(197):20220642. doi: 10.1098/rsif.2022.0642. Epub 2022 Dec 7.

Abstract

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.

Keywords: actin; delta-state; muscle physiology; myosin; skeletal muscle fibre; structural biology; titin.

Publication types

  • Research Support, Non-U.S. Gov't

Associated data

  • figshare/10.6084/m9.figshare.21621132