Department of Anatomy and Neurobiology, Dalhousie University, Halifax, NS, Canada.
Prog Brain Res. 2012;201:313-31. doi: 10.1016/B978-0-444-59544-7.00015-9.
Alpha motor neurons (also known as lower or skeletal motor neurons) have been studied extensively for over 100 years. Motor neurons control the contraction of skeletal muscles and thus are the final common pathway in the nervous system responsible for motor behavior. Muscles become paralyzed when their innervating motor neurons die because of injury or disease. Motor neuron diseases (MNDs), such as Amyotrophic Lateral Sclerosis, progressively destroy motor neurons until those inflicted succumb to the illness due to respiratory failure. One strategy being explored to study and treat muscle paralysis due to motor neuron loss involves deriving surrogate motor neurons from pluripotent stem cells. Guided by decades of research on the development of the spinal cord, recent advances in neurobiology have shown that functional motor neurons can be derived from mouse and human embryonic stem (ES) cells. Furthermore, ES cell-derived motor neurons restore motor behavior when transplanted into animal models of motor dysfunction. The recent discovery that mouse and human motor neurons can be derived from induced pluripotent stem (iPS) cells (i.e., somatic cells converted to pluripotency) has set the stage for the development of patient-specific therapies designed to treat movement disorders. Indeed, there is now hope within the scientific community that motor neurons derived from pluripotent stem cells will be used to treat MNDs through cell transplantation and/or to screen molecules that will prevent motor neuron death. In this chapter, we review the journey that led to the generation of motor neurons from ES and iPS cells, how stem cell-derived motor neurons have been used to treat/study motor dysfunction, and where the technology will likely lead to in the future.
α运动神经元(也称为下运动神经元或躯体运动神经元)已经被研究了超过 100 年。运动神经元控制骨骼肌的收缩,因此是神经系统中负责运动行为的最终共同途径。由于损伤或疾病,支配肌肉的运动神经元死亡,导致肌肉瘫痪。运动神经元疾病(MND),如肌萎缩侧索硬化症,会逐渐破坏运动神经元,直至受影响的患者因呼吸衰竭而屈服于疾病。正在探索的一种研究和治疗因运动神经元丧失导致的肌肉瘫痪的策略是从多能干细胞中衍生替代运动神经元。在对脊髓发育进行了几十年的研究指导下,神经生物学的最新进展表明,可以从小鼠和人类胚胎干细胞(ES 细胞)中衍生出功能性运动神经元。此外,ES 细胞衍生的运动神经元在移植到运动功能障碍的动物模型中时可以恢复运动行为。最近的发现表明,小鼠和人类运动神经元可以从诱导多能干细胞(iPS 细胞)(即体细胞转化为多能性)中衍生出来,这为开发旨在治疗运动障碍的患者特异性疗法奠定了基础。事实上,科学界现在希望利用多能干细胞衍生的运动神经元通过细胞移植来治疗 MNDs,和/或筛选出可防止运动神经元死亡的分子。在本章中,我们将回顾从 ES 和 iPS 细胞生成运动神经元的历程,探讨干细胞衍生的运动神经元如何用于治疗/研究运动功能障碍,以及该技术未来可能的发展方向。