Biral Donatella, Kern Helmut, Adami Nicoletta, Boncompagni Simona, Protasi Feliciano, Carraro Ugo
Italian C.N.R. Institute of Neuroscience, and Laboratory of Translational Myology, Interdepartmental Research Center of Myology, c/o Department of Biomedical Sciences, University of Padova, I-35121 Padova, Italy.
Neurol Res. 2008 Mar;30(2):137-44. doi: 10.1179/174313208X281145.
Human muscle fibers usually undergo severe atrophy/degeneration as a result of long-term peripheral denervation. However, some biopsies from paraplegic patients suffering complete conus cauda syndrome display the presence of a small percentage of muscle fibers with a very large diameter (big fibers). The objective of the present study is to determine if these big fibers are the result of residual innervation/reinnervation, or if instead they are fibers resistant to atrophy.
Human muscle biopsies were harvested from the vastus lateralis of spinal cord injury (SCI) patients affected by complete lower motor neuron lesion (LML). The specimens were either processed for light microscopy or embedded for electron microscopy (EM).
Our results indicate that the big fibers are neither the results of residual innervation or sparse reinnervation. In spite of the fact that the extrasynaptic NCAM immunostaining disappear a few months after SCI, the big fibers are characterized by positive molecular markers of denervation, that is, the differential labeling of their dystrophin molecule by anti-C and anti-N terminals antibodies. Furthermore, the EM analysis shows that these cells present the peculiar ultrastructural disarrangements of the contractile apparatus and of the internal membrane systems characteristic of 'peripheral denervation'. No fibers presenting large areas of cross-striation were found. The EM analysis provides the final evidence that these big fibers are muscle fibers which are indeed denervated, very different from normal and/or disused (e.g. upper motor neuron lesion) muscle fibers.
Although these large muscle fibers are surprisingly more frequent in human muscle biopsies after 3 years from SCI than earlier, it remains to be determined whether their presence in some biopsies but not in others is caused by sampling, or is related to other factors such as to subjects' background genetics, or the extent of passive stretching induced by different rehabilitation strategies.
长期外周去神经支配通常会导致人类肌纤维严重萎缩/变性。然而,一些来自患有完全性马尾圆锥综合征的截瘫患者的活检显示,存在一小部分直径非常大的肌纤维(大纤维)。本研究的目的是确定这些大纤维是残余神经支配/再支配的结果,还是对萎缩具有抗性的纤维。
从患有完全性下运动神经元损伤(LML)的脊髓损伤(SCI)患者的股外侧肌获取人类肌肉活检样本。样本要么进行光镜检查处理,要么包埋用于电子显微镜(EM)检查。
我们的结果表明,大纤维既不是残余神经支配也不是稀疏再支配的结果。尽管突触外神经细胞黏附分子(NCAM)免疫染色在脊髓损伤后几个月消失,但大纤维的特征是去神经支配的阳性分子标记,即抗C端和抗N端抗体对其肌营养不良蛋白分子的差异标记。此外,电子显微镜分析表明,这些细胞呈现出收缩装置和内膜系统特有的“外周去神经支配”的特殊超微结构紊乱。未发现呈现大面积横纹的纤维。电子显微镜分析提供了最终证据,表明这些大纤维确实是去神经支配的肌纤维,与正常和/或废用(如下运动神经元损伤)的肌纤维非常不同。
尽管这些大肌纤维在脊髓损伤3年后的人类肌肉活检中比早期更频繁出现,但仍有待确定它们在一些活检中存在而在其他活检中不存在是由取样引起的,还是与其他因素有关,如受试者的背景遗传学,或不同康复策略引起的被动拉伸程度。