Motion and Exercise Science, University of Stuttgart, Stuttgart, Germany.
Institute of Sport Science, Department of Biomechanics, University of Rostock, Rostock, Germany.
J R Soc Interface. 2022 Dec;19(197):20220642. doi: 10.1098/rsif.2022.0642. Epub 2022 Dec 7.
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.
肌球蛋白纤维在短哺乳动物骨骼肌长度下如何运作尚不清楚。一个常见的假设是,厚(肌球蛋白)纤维在 Z 盘处被压缩。我们提供了超微结构证据,证明在长时间收缩时,肌节收缩到 0.44 µm——大约是厚丝休息长度的四分之一——而明显保持着规则的、平行的厚丝排列。肌节在如此极端的短长度下产生力。此外,肌节采用了双峰长度分布,两个模式都低于经典力-长度测量中预计肌节产生力的长度。正如以前报道的两栖动物纤维一样,哺乳动物纤维在去激活后没有恢复到静息长度,而是保持短缩,并且在被动再伸长过程中显示出增加的力。这些发现与粘弹性厚丝压缩不一致,但与包含厚丝通过 Z 盘滑动的模型的预测一致。这种更连贯的机械哺乳动物骨骼肌纤维功能的图片为肌肉生理学开辟了新的视角。