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GDNF expression is increased in denervated human skeletal muscle.

机译:GDNF表达在失神经的人骨骼肌中增加。

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Glial cell line derived neurotrophic factor (GDNF) is a potent trophic factor for several subpopulations of neurons including motor neurons. Two different transcripts of the GDNF gene (GDNF633 and GDNF555) have been detected in various tissues, including skeletal muscle. Denervation leads to an upregulation of GDNF633 in rat skeletal muscle, indicating that GDNF is involved in the response of skeletal muscle to denervation and possibly in reinnervation. To determine the role of GDNF in human neuromuscular disease, we investigated the expression of both transcripts in normal and denervated muscle and in muscle biopsies from Duchenne muscular dystrophy patients. GDNF expression levels were analyzed by competitive RT-PCR in 38 muscle specimens. Levels of both transcripts were significantly elevated in denervated muscle compared to normal and dystrophic muscle. Morphometric analysis of muscle-fiber calibers and its correlation to GDNF expression revealed that higher levels of GDNF were expressed in rapidly-progressive neurogenic atrophy, including four amyotrophic lateral sclerosis (ALS) cases, compared to cases of chronic atrophy. In dystrophic muscle, transcript levels were not significantly altered compared to normal controls. These data indicate that denervation, but not dystrophy, enhances GDNF expression in human skeletal muscle. Thus, the increase of GDNF expression is part of the reaction of human skeletal muscle to denervation caused by motor nerve lesion. GDNF might act on regenerating nerve fibers during muscle fiber reinnervation.
机译:胶质细胞系衍生的神经营养因子(GDNF)是神经元包括运动神经元的几个亚群的有效营养因子。已在包括骨骼肌在内的各种组织中检测到GDNF基因的两个不同转录本(GDNF633和GDNF555)。去神经支配导致大鼠骨骼肌中GDNF633的上调,表明GDNF参与了骨骼肌对神经支配的反应,并可能参与了神经支配。为了确定GDNF在人神经肌肉疾病中的作用,我们调查了正常和非神经支配的肌肉以及Duchenne肌营养不良患者的肌肉活检中转录本的表达。通过竞争性RT-PCR分析了38个肌肉样本中的GDNF表达水平。与正常和营养不良的肌肉相比,神经支配的肌肉中两种转录物的水平均显着升高。肌纤维口径的形态计量学分析及其与GDNF表达的相关性表明,与慢性萎缩病例相比,快速进展的神经源性萎缩(包括4例肌萎缩性侧索硬化症(ALS)病例)表达了更高水平的GDNF。在营养不良的肌肉中,与正常对照组相比,转录水平没有明显改变。这些数据表明,去神经作用而非营养不良会增强人骨骼肌中GDNF的表达。因此,GDNF表达的增加是人骨骼肌对由运动神经病变引起的神经支配反应的一部分。 GDNF可能在肌肉纤维神经支配期间作用于再生神经纤维。

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