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Interrelations of myogenic response, progressive atrophy of muscle fibers, and cell death in denervated skeletal muscle

机译:肌源性反应,肌纤维进行性萎缩和失神经支配骨骼肌细胞死亡的相互关系

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摘要

Little is known concerning the time-course and structural dynamics of reactivation of compensatory myogenesis in denervated muscle, its initiating cellular mechanisms, and the relationship between this process and the progression of postdenervation atrophy. The purpose of this study was to investigate the interrelations between temporal and spatial patterns of the myogenic response in denervated muscle and progressive atrophy of muscle fibers. Another objective was to study whether reactivation of myogenesis correlates with destabilization of the differentiated state and death of denervated muscle cells. It has remained unclear whether muscle fiber atrophy was the primary factor activating the myogenic response, what levels of cellular atrophy were associated with its activation, and whether the initiation and intensity of myogenesis depended on the local and individual heterogeneity of atrophic changes among fibers. For this reason, our objective was also to identify the levels of atrophic and degenerative changes in denervated muscle fibers that are correlated with activation of the myogenic response. We found that the reactivation of myogenesis in the tibialis anterior and extensor digitorum longus muscles of the rat starts between days 10–21 following nerve transection, before atrophy has attained advanced level, long before dead cells are found in the tissue. Formation of new muscle fibers reaches its maximum between 2 and 4 months following denervation and gradually decreases with progressive postdenervation atrophy. The myogenic response is biphasic and includes two distinct processes. The first process resembles the formation of secondary and tertiary generations of myotubes during normal muscle development and dominates during the first 2 months of denervation. During this period, activated satellite cells form new myotubes on live differentiated muscle fibers. Most of the daughter myotubes in 1- and 2-month denervated muscle develop on the surface of fast type parent muscle fibers, and some of the newly formed muscle fibers express slow myosin. Some fast type parent fibers are weakly or, more rarely, moderately immunopositive for embryonic isomyosin. This indicates that reactivation of myogenesis may also depend on the fiber type. The level of atrophy, destabilization of the differentiated myofiber phenotype, and degenerative changes of individual fibers in denervated muscle are very heterogeneous. The myogenic response of the first type is associated predominantly with fibers of average and higher than average levels of atrophy. Muscle cells that undergo a lesser degree of atrophy also form daughter fibers, although with a lower incidence. We did not find any correlation between the size of newly formed fibers and the level of atrophy of parent fibers. The topographical distribution of new myotubes both in the peripheral and central areas of the mid-belly equatorial sections at the early stages following nerve transection indicates that myogenesis of the first type represents a systemic reaction of muscle to the loss of neural control. These data indicate that activation of the myogenic response does not depend on cell death and degenerative processes per se. The second type of myogenesis is a typical regenerative reaction that occurs mainly within the spaces surrounded by the basal laminae of dead muscle fibers. Myocytes of different sizes are susceptible to degeneration and death, which indicates that cell death in denervated muscle does not correlate with levels of muscle cell atrophy. The regenerative process frequently results in development of abnormal muscle cells that branch or form small clusters. Replacement of lost fibers becomes activated between 2 and 4 months following nerve transection, i.e., mainly at advanced stages of postdenervation atrophy, when cell death becomes a contributing factor of the atrophic process. In long-term denervated muscle, the first and second types of myogenesisoccur concurrently, and the topographical distribution of the myogenic response becomes more heterogeneous than during the first weeks following denervation. Thus, our data demonstrate differential temporal and spatial expression of two patterns of myogenesis in denervated muscle that appear to be controlled by different regulatory mechanisms during the postdenervation period. Anat Rec 264:203–218, 2001. © 2001 Wiley-Liss, Inc.
机译:关于失神经肌肉中代偿性肌生成的重新激活的时程和结构动力学,其启动的细胞机制以及该过程与去神经后萎缩进展之间的关系,人们所知甚少。这项研究的目的是调查失神经的肌肉中肌反应的时空模式与肌纤维进行性萎缩之间的相互关系。另一个目的是研究肌再生的恢复是否与分化状态的不稳定和失神经的肌肉细胞的死亡有关。尚不清楚肌纤维萎缩是否是激活肌源性反应的主要因素,什么水平的细胞萎缩与其激活相关,以及肌发生的起始和强度是否取决于纤维间萎缩性改变的局部和个体异质性。出于这个原因,我们的目标也是确定与肌源性反应的激活相关的失神经肌纤维萎缩和退行性改变的水平。我们发现,大鼠的胫骨前肌和指长肌的肌再生在神经横断后10-21天之间开始,在萎缩达到进展水平之前,早在组织中发现死细胞之前。去神经后2到4个月之间,新的肌肉纤维形成达到最大,随着去神经后萎缩逐渐减少。成肌反应是双相的,包括两个不同的过程。第一个过程类似于正常肌肉发育过程中第二代和第三代肌管的形成,在去神经的前两个月中占主导地位。在此期间,活化的卫星细胞在分化的活肌纤维上形成新的肌管。在1个月和2个月失神经的肌肉中,大多数子代肌管在快速型母体肌纤维的表面上发育,并且一些新形成的肌纤维表达慢肌球蛋白。一些快速型母体纤维对胚胎异肌球蛋白的免疫力较弱,或更罕见。这表明肌发生的再激活也可能取决于纤维类型。萎缩的程度,分化的肌纤维表型的失稳以及失神经肌肉中单个纤维的变性变化非常不均匀。第一种类型的肌源性反应主要与平均水平和高于平均萎缩水平的纤维相关。萎缩程度较小的肌肉细胞也形成子纤维,尽管发生率较低。我们没有发现新形成的纤维的尺寸和母体纤维萎缩的水平之间有任何相关性。新的肌管在神经横断后早期在中腹部赤道中段的外围和中央区域的地形分布表明,第一类肌发生代表肌肉对神经控制丧失的系统性反应。这些数据表明,肌原性应答的激活并不取决于细胞死亡和变性过程本身。第二种类型的肌发生是典型的再生反应,主要发生在死肌纤维基底层所包围的空间内。不同大小的肌细胞易于变性和死亡,这表明失神经肌肉中的细胞死亡与肌肉细胞萎缩程度无关。再生过程经常导致分支或形成小簇的异常肌肉细胞的发育。在神经横断后的2到4个月之间,即主要在去神经后萎缩的晚期,当细胞死亡成为萎缩过程的一个促成因素时,丢失的纤维的置换被激活。在长期失神经的肌肉中,第一和第二类型的肌发生同时发生,并且与失神经后的最初几周相比,成肌反应的地形分布变得更加不均匀。因此,我们的数据证明了去神经后肌肉中两种肌肉生成模式的时空差异表达,这两种模式似乎受不同的调节机制控制。 Anat Rec 264:203–218,2001。©2001 Wiley-Liss,Inc.。

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