Department of Pharmacology and Systems Physiology, University of Cincinnati, Cincinnati, Ohio.
Eur J Neurosci. 2019 May;49(9):1084-1090. doi: 10.1111/ejn.14304. Epub 2018 Dec 27.
Expression of the ciliary neurotrophic factor (CNTF) receptor essential ligand binding subunit, CNTF receptor α (CNTFRα), is induced in motor neurons and skeletal muscle following peripheral nerve lesion. We previously found muscle CNTFRα promotes motor neuron axon regeneration post-lesion. Both nerve lesion and CNTF administration activate motor neuron signal transducer and activator of transcription 3 (STAT3), a transcription factor implicated in axon growth, suggesting CNTF receptors may contribute to the lesion-induced STAT3 activation. However, many receptor types signal through STAT3, and if CNTF receptors contribute, motor neuron receptors seemed most likely to regulate motor neuron STAT3. To determine the role played by muscle CNTFRα, we used in vivo, muscle-specific CNTFRα depletion in mice and report here that this selectively impairs the second phase, sustained motor neuron STAT3 activation post-lesion. Thus, muscle CNTFRα makes an essential contribution to motor neuron STAT3 activation during axon regeneration and may thereby promote axon regeneration through such signaling. We also report CNTFRα quantitative PCR suggesting involvement of many denervated muscle types, as well as muscle damaged at the lesion site. The present data add to the evidence suggesting that enhancing muscle CNTFRα expression may promote motor neuron regeneration in trauma and disease.
睫状神经营养因子 (CNTF) 受体必需配体结合亚基 (CNTFRα) 的表达在外周神经损伤后在运动神经元和骨骼肌中被诱导。我们之前发现肌肉 CNTFRα 促进损伤后运动神经元轴突再生。神经损伤和 CNTF 给药都激活运动神经元信号转导和转录激活因子 3 (STAT3),这是一种与轴突生长有关的转录因子,表明 CNTF 受体可能有助于损伤诱导的 STAT3 激活。然而,许多受体类型通过 STAT3 发出信号,如果 CNTF 受体起作用,运动神经元受体似乎最有可能调节运动神经元 STAT3。为了确定肌肉 CNTFRα 所起的作用,我们在小鼠中使用了体内肌肉特异性 CNTFRα 耗竭,并在此报告说,这选择性地损害了损伤后第二阶段持续的运动神经元 STAT3 激活。因此,肌肉 CNTFRα 对运动神经元 STAT3 激活在轴突再生过程中起着至关重要的作用,并且可能通过这种信号转导促进轴突再生。我们还报告了 CNTFRα 的定量 PCR,表明许多去神经支配的肌肉类型以及损伤部位的肌肉都参与其中。目前的数据增加了证据表明,增强肌肉 CNTFRα 的表达可能促进创伤和疾病中的运动神经元再生。