Mendoza Andrea C, Rassier Dilson E
Department of Kinesiology and Physical Education, McGill University, Montreal, Quebec, Canada.
Department of Kinesiology and Physical Education, McGill University, Montreal, Quebec, Canada.
Biophys J. 2020 Apr 21;118(8):1921-1929. doi: 10.1016/j.bpj.2020.03.007. Epub 2020 Mar 19.
It has been accepted that the force produced by a skeletal muscle myofibril depends on its cross-sectional area but not on the number of active sarcomeres because they are arranged in series. However, a previous study performed by our group showed that blocking actomyosin interactions within an activated myofibril and depleting the thick filaments in one sarcomere unexpectedly reduced force production. In this study, we examined in detail how consecutive depletion of thick filaments in individual sarcomeres within a myofibril affects force production. Myofibrils isolated from rabbit psoas were activated and relaxed using a perfusion system. An extra microperfusion needle filled with a high-ionic strength solution was used to erase thick filaments in individual sarcomeres in real time before myofibril activation. The isometric forces were measured upon activation. The force produced by myofibrils with intact sarcomeres was significantly higher than the force produced by myofibrils with one or more sarcomeres lacking thick filaments (p < 0.0001) irrespective of the number of contractions imposed on the myofibrils and their initial sarcomere length. Our results suggest that the myofibril force is affected by intersarcomere dynamics and the number of active sarcomeres in series.
人们已经公认,骨骼肌肌原纤维产生的力量取决于其横截面积,而不取决于活跃肌节的数量,因为它们是串联排列的。然而,我们小组之前进行的一项研究表明,阻断激活的肌原纤维内的肌动球蛋白相互作用以及耗尽一个肌节中的粗肌丝,意外地降低了力量产生。在本研究中,我们详细研究了肌原纤维内单个肌节中粗肌丝的连续耗尽如何影响力量产生。从兔腰大肌分离的肌原纤维使用灌注系统进行激活和松弛。在肌原纤维激活前,使用一根额外的充满高离子强度溶液的微灌注针实时消除单个肌节中的粗肌丝。在激活时测量等长力。无论对肌原纤维施加的收缩次数及其初始肌节长度如何,具有完整肌节的肌原纤维产生的力量显著高于具有一个或多个缺乏粗肌丝的肌节的肌原纤维产生的力量(p < 0.0001)。我们的结果表明,肌原纤维力量受肌节间动力学和串联活跃肌节数量的影响。