BioCAT, Department of Biology, Illinois Institute of Technology, Chicago, IL, USA.
Department of Bioengineering, University of Washington, Seattle, WA, USA.
J Physiol. 2022 Dec;600(24):5247-5266. doi: 10.1113/JP283574. Epub 2022 Nov 23.
The contractile properties of fast-twitch and slow-twitch skeletal muscles are primarily determined by the myosin isoform content and modulated by a variety of sarcomere proteins. X-ray diffraction studies of regulatory mechanisms in muscle contraction have focused predominately on fast- or mixed-fibre muscle with slow muscle being much less studied. Here, we used time-resolved X-ray diffraction to investigate the dynamic behaviour of the myofilament proteins in relatively pure slow-twitch-fibre rat soleus (SOL) and pure fast-twitch-fibre rat extensor digitorum longus (EDL) muscle during twitch and tetanic contractions at optimal length. During twitch contractions the diffraction signatures indicating a transition in the myosin heads from ordered OFF states, where heads are held close to the thick filament backbone, to disordered ON states, where heads are free to bind to thin filaments, were found in EDL and not in SOL muscle. During tetanic contraction, changes in the disposition of myosin heads as active tension develops is a quasi-stepwise process in EDL muscle whereas in SOL muscle this relationship appears to be linear. The observed reduced extensibility of the thick filaments in SOL muscle as compared to EDL muscles indicates a molecular basis for this behaviour. These data indicate that for the EDL, thick filament activation is a cooperative strain-induced mechano-sensing mechanism, whereas for the SOL, thick filament activation has a more graded response. These different approaches to thick filament regulation in fast- and slow-twitch muscles may be adaptations for short-duration, strong contractions versus sustained, finely controlled contractions, respectively. KEY POINTS: Fast-twitch muscle and slow-twitch muscle are optimized for strong, short-duration contractions and for tonic postural activity, respectively. Structural events (OFF to ON transitions) in the myosin-containing thick filaments in fast muscle help determine the timing and strength of contractions, but these have not been studied in slow-twitch muscle. The X-ray diffraction signatures of structural OFF to ON transitions are different in fast extensor digitorum longus (EDL) and slow soleus (SOL) muscle, being completely absent during twitches in soleus muscle and blunted during tetanic contractions SOL as compared to EDL Quasi-stepwise thick filament structural OFF to ON transitions in fast twitch muscle may be an adaptation for rapid, ballistic movements, whereas more graded OFF to ON structural transitions in slow-twitch muscle may be an adaptation for slower, finer motions.
快肌和慢肌的收缩特性主要由肌球蛋白同工型含量决定,并受各种肌节蛋白调节。肌肉收缩调节机制的 X 射线衍射研究主要集中在快肌或混合纤维肌,而慢肌的研究则要少得多。在这里,我们使用时间分辨 X 射线衍射技术,在最佳长度下,研究相对纯慢肌大鼠比目鱼肌(SOL)和纯快肌大鼠趾长伸肌(EDL)肌肉在抽搐和强直性收缩过程中肌丝蛋白的动态行为。在抽搐收缩过程中,发现 ED L 肌肉中肌球蛋白头部从有序的 OFF 状态(头部靠近粗肌丝主干)转变为无序的 ON 状态(头部可以自由结合细肌丝)的衍射特征,但在 SOL 肌肉中没有发现。在强直性收缩过程中,随着主动张力的发展,肌球蛋白头部的位置变化是一个准逐步的过程,而在 SOL 肌肉中,这种关系似乎是线性的。与 EDL 肌肉相比,SOL 肌肉中粗丝的伸展性降低表明了这种行为的分子基础。这些数据表明,对于 EDL,粗丝的激活是一种协同应变诱导的机械感觉机制,而对于 SOL,粗丝的激活具有更分级的反应。这些快肌和慢肌中粗丝调节的不同方法可能分别是适应短时间、强收缩和持续、精细控制收缩的结果。关键点:快肌和慢肌分别优化用于强、短时间收缩和用于紧张姿势活动。在快肌中,含有肌球蛋白的粗丝中的结构事件(OFF 到 ON 转变)有助于确定收缩的时间和强度,但在慢肌中尚未研究这些事件。在快肌伸肌 digitorum longus(EDL)和慢肌比目鱼肌(SOL)中,结构 OFF 到 ON 转变的 X 射线衍射特征不同,在 SOL 肌肉的抽搐过程中完全不存在,而在强直性收缩 SOL 中则变钝与 EDL 相比,快肌中的准逐步粗丝结构 OFF 到 ON 转变可能是快速、弹道运动的适应,而慢肌中较慢、较精细运动的更分级 OFF 到 ON 结构转变可能是一种适应。