S. Dayanidhi, M. C. Kinney, R. L. Lieber, Department of Orthopaedic Surgery, University of California, San Diego, CA, USA.
S. Dayanidhi, R. L. Lieber, Department of Veterans Affairs Medical Center, San Diego, CA, USA.
Clin Orthop Relat Res. 2020 Apr;478(4):886-899. doi: 10.1097/CORR.0000000000001134.
Children with cerebral palsy have impaired muscle growth and muscular contractures that limit their ROM. Contractures have a decreased number of serial sarcomeres and overstretched lengths, suggesting an association with a reduced ability to add the serial sarcomeres required for normal postnatal growth. Contractures also show a markedly reduced number of satellite cells-the muscle stem cells that are indispensable for postnatal muscle growth, repair, and regeneration. The potential role of the reduced number of muscle stem cells in impaired sarcomere addition leading to contractures must be evaluated.
QUESTIONS/PURPOSES: (1) Does a reduced satellite cell number impair the addition of serial sarcomeres during recovery from an immobilization-induced contracture? (2) Is the severity of contracture due to the decreased number of serial sarcomeres or increased collagen content?
The hindlimbs of satellite cell-specific Cre-inducible mice (Pax7; Rosa26; n = 10) were maintained in plantarflexion with plaster casts for 2 weeks so that the soleus was chronically shortened and the number of its serial sarcomeres was reduced by approximately 20%. Subsequently, mice were treated with either tamoxifen to reduce the number of satellite cells or a vehicle (an injection and handling control). The transgenic mouse model with satellite cell ablation combined with a casting model to reduce serial sarcomere number recreates two features observed in muscular contractures in children with cerebral palsy. After 30 days, the casts were removed, the mice ankles were in plantarflexion, and the mice's ability to recover its ankle ROM by cage remobilization for 30 days were evaluated. We quantified the number of serial sarcomeres, myofiber area, and collagen content of the soleus muscle as well as maximal ankle dorsiflexion at the end of the recovery period.
Mice with reduced satellite cell numbers did not regain normal ankle ROM in dorsiflexion; that is, the muscles remained in plantarflexion contracture (-16° ± 13° versus 31° ± 39° for the control group, -47 [95% confidence interval -89 to -5]; p = 0.03). Serial sarcomere number of the soleus was lower on the casted side than the contralateral side of the mice with a reduced number of satellite cells (2214 ± 333 versus 2543 ± 206, -329 [95% CI -650 to -9]; p = 0.04) but not different in the control group (2644 ± 194 versus 2729 ± 249, -85 [95% CI -406 to 236]; p = 0.97). The degree of contracture was strongly associated with the number of sarcomeres and myofiber area (r =0.80; P < 0.01) rather than collagen content. No differences were seen between groups in terms of collagen content and the fraction of muscle area.
We found that a reduced number of muscle stem cells in a transgenic mouse model impaired the muscle's ability to add sarcomeres in series and thus to recover from an immobilization-induced contracture.
The results of our study in transgenic mouse muscle suggests there may be a mechanistic relationship between a reduced number of satellite cells and a reduced number of serial sarcomeres. Contracture development, secondary to impaired sarcomere addition in muscles in children with cerebral palsy may be due to a reduced number of muscle stem cells.
脑瘫患儿的肌肉生长受损,肌肉挛缩限制了其关节活动度。挛缩导致串联肌节数量减少和过度拉伸长度,这表明与正常出生后生长所需的串联肌节数量减少有关。挛缩还显示出明显减少的卫星细胞数量 - 肌肉干细胞,对于出生后肌肉生长、修复和再生是必不可少的。必须评估肌肉干细胞数量减少对导致挛缩的串联肌节添加的影响。
问题/目的:(1)卫星细胞数量减少是否会在固定诱导挛缩的恢复过程中损害串联肌节的添加?(2)挛缩的严重程度是由于串联肌节数量减少还是胶原含量增加?
将卫星细胞特异性 Cre 诱导型小鼠(Pax7; Rosa26; n = 10)的后肢用石膏固定在跖屈位 2 周,使比目鱼肌长期缩短,其串联肌节数量减少约 20%。随后,用他莫昔芬或载体(注射和处理对照)处理小鼠以减少卫星细胞数量。结合铸造模型减少串联肌节数量的卫星细胞消融转基因小鼠模型再现了脑瘫患儿肌肉挛缩中观察到的两个特征。30 天后,去除石膏,小鼠踝关节跖屈,通过笼内再动员 30 天评估小鼠恢复踝关节 ROM 的能力。我们量化了比目鱼肌的串联肌节数量、肌纤维面积和胶原含量以及恢复期末部的最大踝关节背屈。
卫星细胞数量减少的小鼠不能恢复正常的踝关节背屈 ROM;也就是说,肌肉仍然处于跖屈挛缩状态(与对照组相比,-16°±13°与 31°±39°,-47 [95%置信区间-89 至-5];p = 0.03)。与对照组相比,卫星细胞数量减少的小鼠的比目鱼肌的串联肌节数量较少(2214 ± 333 与 2543 ± 206,-329 [95%CI-650 至-9];p = 0.04),但在对照组中没有差异(2644 ± 194 与 2729 ± 249,-85 [95%CI-406 至 236];p = 0.97)。挛缩的程度与肌节和肌纤维面积的数量密切相关(r = 0.80; P <0.01),而与胶原含量无关。在胶原含量和肌肉面积分数方面,各组之间没有差异。
我们发现,转基因小鼠模型中肌肉干细胞数量减少损害了肌肉添加串联肌节的能力,从而无法从固定诱导的挛缩中恢复。
我们在转基因小鼠肌肉中的研究结果表明,卫星细胞数量减少与串联肌节数量减少之间可能存在机制关系。脑瘫患儿肌肉挛缩的发展可能是由于肌肉干细胞数量减少导致的肌节添加受损。