División de Neurociencias, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México Mexico City, Mexico.
Front Cell Neurosci. 2014 Feb 28;8:61. doi: 10.3389/fncel.2014.00061. eCollection 2014.
Motor neuron physiology and development depend on a continuous and tightly regulated trophic support from a variety of cellular sources. Trophic factors guide the generation and positioning of motor neurons during every stage of the developmental process. As well, they are involved in axon guidance and synapse formation. Even in the adult spinal cord an uninterrupted trophic input is required to maintain neuronal functioning and protection from noxious stimuli. Among the trophic factors that have been demonstrated to participate in motor neuron physiology are vascular endothelial growth factor (VEGF), glial-derived neurotrophic factor (GDNF), ciliary neurotrophic factor (CNTF) and insulin-like growth factor 1 (IGF-1). Upon binding to membrane receptors expressed in motor neurons or neighboring glia, these trophic factors activate intracellular signaling pathways that promote cell survival and have protective action on motor neurons, in both in vivo and in vitro models of neuronal degeneration. For these reasons these factors have been considered a promising therapeutic method for amyotrophic lateral sclerosis (ALS) and other neurodegenerative diseases, although their efficacy in human clinical trials have not yet shown the expected protection. In this minireview we summarize experimental data on the role of these trophic factors in motor neuron function and survival, as well as their mechanisms of action. We also briefly discuss the potential therapeutic use of the trophic factors and why these therapies may have not been yet successful in the clinical use.
运动神经元的生理和发育依赖于各种细胞来源的持续和严格调节的营养支持。营养因子在发育过程的每个阶段指导运动神经元的产生和定位。它们还参与轴突导向和突触形成。即使在成年脊髓中,也需要不间断的营养输入来维持神经元的功能并防止有害刺激。已经证明参与运动神经元生理学的营养因子包括血管内皮生长因子 (VEGF)、胶质衍生神经营养因子 (GDNF)、睫状神经营养因子 (CNTF) 和胰岛素样生长因子 1 (IGF-1)。这些营养因子与运动神经元或邻近神经胶质细胞中表达的膜受体结合后,会激活细胞内信号通路,促进细胞存活,并对运动神经元具有保护作用,无论是在体内还是体外的神经元退化模型中。由于这些原因,这些因子被认为是肌萎缩侧索硬化症 (ALS) 和其他神经退行性疾病的有前途的治疗方法,尽管它们在人类临床试验中的疗效尚未显示出预期的保护作用。在这篇综述中,我们总结了这些营养因子在运动神经元功能和存活中的作用及其作用机制的实验数据。我们还简要讨论了营养因子的潜在治疗用途,以及为什么这些疗法在临床应用中尚未成功。