Dupuis Luc, Gonzalez de Aguilar Jose-Luis, Echaniz-Laguna Andoni, Eschbach Judith, Rene Frédérique, Oudart Hugues, Halter Benoit, Huze Caroline, Schaeffer Laurent, Bouillaud Frédéric, Loeffler Jean-Philippe
Inserm, U692, Laboratoire de Signalisations Moléculaires et Neurodégénérescence, Strasbourg, France.
PLoS One. 2009;4(4):e5390. doi: 10.1371/journal.pone.0005390. Epub 2009 Apr 30.
Amyotrophic lateral sclerosis (ALS), the most frequent adult onset motor neuron disease, is associated with hypermetabolism linked to defects in muscle mitochondrial energy metabolism such as ATP depletion and increased oxygen consumption. It remains unknown whether muscle abnormalities in energy metabolism are causally involved in the destruction of neuromuscular junction (NMJ) and subsequent motor neuron degeneration during ALS.
METHODOLOGY/PRINCIPAL FINDINGS: We studied transgenic mice with muscular overexpression of uncoupling protein 1 (UCP1), a potent mitochondrial uncoupler, as a model of muscle restricted hypermetabolism. These animals displayed age-dependent deterioration of the NMJ that correlated with progressive signs of denervation and a mild late-onset motor neuron pathology. NMJ regeneration and functional recovery were profoundly delayed following injury of the sciatic nerve and muscle mitochondrial uncoupling exacerbated the pathology of an ALS animal model.
CONCLUSIONS/SIGNIFICANCE: These findings provide the proof of principle that a muscle restricted mitochondrial defect is sufficient to generate motor neuron degeneration and suggest that therapeutic strategies targeted at muscle metabolism might prove useful for motor neuron diseases.
肌萎缩侧索硬化症(ALS)是最常见的成人起病运动神经元疾病,与肌肉线粒体能量代谢缺陷相关的高代谢有关,如ATP耗竭和氧消耗增加。目前尚不清楚能量代谢中的肌肉异常是否在ALS期间因果性地参与神经肌肉接头(NMJ)的破坏及随后的运动神经元变性。
方法/主要发现:我们研究了肌肉过度表达解偶联蛋白1(UCP1,一种有效的线粒体解偶联剂)的转基因小鼠,作为肌肉限制性高代谢的模型。这些动物表现出与去神经支配的进行性体征相关的NMJ年龄依赖性退化以及轻度迟发性运动神经元病理改变。坐骨神经损伤后,NMJ再生和功能恢复显著延迟,并且肌肉线粒体解偶联加剧了ALS动物模型的病理改变。
结论/意义:这些发现提供了原则性证据,即肌肉限制性线粒体缺陷足以导致运动神经元变性,并表明针对肌肉代谢的治疗策略可能对运动神经元疾病有用。