Kääriäinen M, Järvinen T, Järvinen M, Rantanen J, Kalimo H
Medical School and the Institute of Medical Technology, University of Tampere, Finland.
Scand J Med Sci Sports. 2000 Dec;10(6):332-7. doi: 10.1034/j.1600-0838.2000.010006332.x.
The connective tissue framework in skeletal muscle combines the contractile myofibers into a functional unit, in which the contraction of myofibers is transformed into movement via myotendinous junctions (MTJs) at their ends, where myofibers attach to tendons/fascia. The cytoskeletal contractile myofilament apparatus adheres through subsarcolemmal and transmembrane molecules to the surrounding extracellular matrix, with integrin and dystrophin associated chains of molecules being the two main adhesion complexes. In shearing type of muscle injury both myofibers and the connective tissue framework are ruptured and thereby the functional tendon-muscle-tendon units are disrupted. The stumps of the ruptured myofibers are separated and at the same time joined by a connective tissue scar, through which the ends of regenerating myofibers try to pierce, but as the scar becomes more compact the ends attach to the scar by new mini-MTJs. During the early phase ruptured myofibers try to compensate for the lost MTJ attachment by reinforcing their integrin mediated lateral adhesion, which returns to normal low level after formation of the mini-MTJs and at which time complementary increase of dystrophin and associated molecules on lateral sarcolemma takes place. The stumps appear to remain separated by and attached to the interposed scar for many months, possibly for ever, i.e. the original tendon-muscle-tendon units may have become permanently divided into two consecutive units. Remarkably, axon sprouts are able to penetrate through the interposed scar to form new neuromuscular junctions on those abjunctional stumps which were denervated by the rupture.
骨骼肌中的结缔组织框架将收缩性肌纤维组合成一个功能单元,在这个单元中,肌纤维的收缩通过其末端的肌-腱连接(MTJ)转化为运动,肌纤维在末端附着于肌腱/筋膜。细胞骨架收缩性肌丝装置通过肌膜下和跨膜分子与周围的细胞外基质相连,整合素和肌营养不良蛋白相关分子链是两个主要的黏附复合体。在剪切型肌肉损伤中,肌纤维和结缔组织框架都会断裂,从而使功能性的肌腱-肌肉-肌腱单元遭到破坏。断裂肌纤维的残端分离,同时由结缔组织瘢痕连接,再生肌纤维的末端试图穿过瘢痕,但随着瘢痕变得更加致密,末端通过新的微型MTJ附着于瘢痕。在早期阶段,断裂的肌纤维试图通过增强整合素介导的侧向黏附来弥补失去的MTJ附着,在微型MTJ形成后,侧向黏附恢复到正常的低水平,此时肌膜外侧的肌营养不良蛋白及相关分子会互补性增加。残端似乎会被插入的瘢痕分隔并附着数月,甚至可能永远如此,即原来的肌腱-肌肉-肌腱单元可能已永久分为两个连续的单元。值得注意的是,轴突芽能够穿透插入的瘢痕,在那些因断裂而失神经支配的非连接残端上形成新的神经肌肉接头。