muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons肌肉线粒体解偶联放弃神经肌肉接头和触发器远端运动神经元的变性.pdfVIP
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muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons肌肉线粒体解偶联放弃神经肌肉接头和触发器远端运动神经元的变性
Muscle Mitochondrial Uncoupling Dismantles Neuromuscular Junction and Triggers Distal Degeneration of Motor Neurons Luc Dupuis1,2*, Jose-Luis Gonzalez de Aguilar1,2, Andoni Echaniz-Laguna1,2,3, Judith Eschbach1,2, ´ ´ 1,2 4 1,2 5 5 ´ ´ Frederique Rene , Hugues Oudart , Benoit Halter , Caroline Huze , Laurent Schaeffer , Frederic Bouillaud6, Jean-Philippe Loeffler1,2* ´ ´ ´ ´ ´ ´ ´ 1 Inserm, U692, Laboratoire de Signalisations Moleculaires et Neurodegenerescence, Strasbourg, France, 2 Universite de Strasbourg, Faculte de Medecine, UMRS692, ˆ ´ Strasbourg, France, 3 Hopitaux Universitaires de Strasbourg, France, 4 DEPE, IPHC, Strasbourg, France, 5 Equipe Differenciation Neuromusculaire, IFR128, UMR5161, ENS ´ ´ ´ ´ Lyon, CNRS, INRA, Universite de Lyon, Lyon, France, 6 BIOTRAM, Universite Paris Descartes, CNRS UPR9078, Faculte de Medecine Necker-Enfants Malades, Paris, France Abstract Background: 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:
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