College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, China.
Department of Biology, Illinois Institute of Technology, Chicago, IL, USA.
J Physiol. 2024 Jun;602(12):2751-2762. doi: 10.1113/JP286072. Epub 2024 May 2.
There is a growing appreciation that regulation of muscle contraction requires both thin filament and thick filament activation in order to fully activate the sarcomere. The prevailing mechano-sensing model for thick filament activation was derived from experiments on fast-twitch muscle. We address the question whether, or to what extent, this mechanism can be extrapolated to the slow muscle in the hearts of large mammals, including humans. We investigated the similarities and differences in structural signatures of thick filament activation in porcine myocardium as compared to fast rat extensor digitorum longus (EDL) skeletal muscle under relaxed conditions and sub-maximal contraction using small angle X-ray diffraction. Thick and thin filaments were found to adopt different structural configurations under relaxing conditions, and myosin heads showed different changes in configuration upon sub-maximal activation, when comparing the two muscle types. Titin was found to have an X-ray diffraction signature distinct from those of the overall thick filament backbone, and its spacing change appeared to be positively correlated to the force exerted on the thick filament. Structural changes in fast EDL muscle were found to be consistent with the mechano-sensing model. In porcine myocardium, however, the structural basis of mechano-sensing is blunted suggesting the need for additional activation mechanism(s) in slow cardiac muscle. These differences in thick filament regulation can be related to their different physiological roles where fast muscle is optimized for rapid, burst-like, contractions, and the slow cardiac muscle in large mammalian hearts adopts a more finely tuned, graded response to allow for their substantial functional reserve. KEY POINTS: Both thin filament and thick filament activation are required to fully activate the sarcomere. Thick and thin filaments adopt different structural configurations under relaxing conditions, and myosin heads show different changes in configuration upon sub-maximal activation in fast extensor digitorum longus muscle and slow porcine cardiac muscle. Titin has an X-ray diffraction signature distinct from those of the overall thick filament backbone and this titin reflection spacing change appeared to be directly proportional to the force exerted on the thick filament. Mechano-sensing is blunted in porcine myocardium suggesting the need for additional activation mechanism(s) in slow cardiac muscle. Fast skeletal muscle is optimized for rapid, burst-like contractions, and the slow cardiac muscle in large mammalian hearts adopts a more finely tuned graded response to allow for their substantial functional reserve.
人们越来越认识到,为了充分激活肌节,肌肉收缩的调节既需要细丝也需要粗丝的激活。目前关于粗丝激活的机械传感模型源自对快肌的实验。我们要探讨的问题是,这种机制是否可以被推断到包括人类在内的大型哺乳动物的慢肌,以及可以推断到何种程度。我们使用小角 X 射线衍射技术,研究了猪心肌与大鼠快速伸趾长肌(EDL)骨骼在放松和次最大收缩状态下粗丝激活的结构特征的异同。结果发现,在放松状态下,粗丝和细丝采用不同的结构构象,而在比较两种肌肉类型时,肌球蛋白头部在次最大激活时的构象发生了不同的变化。发现titin 的 X 射线衍射特征与整体粗丝骨干不同,并且其间距变化似乎与作用在粗丝上的力呈正相关。快速 EDL 肌肉的结构变化与机械传感模型一致。然而,在猪心肌中,机械传感的结构基础较为迟钝,这表明在慢心肌中需要额外的激活机制。这些粗丝调节方面的差异可能与其不同的生理功能有关,其中快肌被优化用于快速、爆发式收缩,而大型哺乳动物心脏的慢心肌则采用更精细的、分级的反应来适应其大量的功能储备。关键点:为了充分激活肌节,既需要细丝也需要粗丝的激活。在快速伸趾长肌和慢速猪心肌中,放松状态下粗丝和细丝采用不同的结构构象,而肌球蛋白头部在次最大激活时的构象发生了不同的变化。titin 的 X 射线衍射特征与整体粗丝骨干不同,并且该 titin 反射间距变化似乎与作用在粗丝上的力呈直接比例关系。猪心肌的机械传感较为迟钝,这表明在慢心肌中需要额外的激活机制。快肌被优化用于快速、爆发式收缩,而大型哺乳动物心脏的慢心肌则采用更精细的、分级的反应来适应其大量的功能储备。