首页> 外文期刊>Amyotrophic lateral sclerosis and other motor neuron disorders: Official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases >Motoneuron cell death and neurotrophic factors: Basic models for development of new therapeutic strategies in ALS
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Motoneuron cell death and neurotrophic factors: Basic models for development of new therapeutic strategies in ALS

机译:运动神经元细胞死亡和神经营养因子:ALS新治疗策略发展的基本模型

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Motoneurons are generated in excess during embryonic development of higher vertebrates. In the lumbar spinal cord of the developing rat, about 6000 motoneurons are present at embryonic day 14. These neurons grow out axons which make contact with their target tissue, the skeletal muscle. About 50% of the motoneurons are lost during a critical period from embryonic day 14 until postnatal day 3. This process which is called physiological motoneuron cell death, has been the focus of research aiming at the identification of neurotrophic factors which regulate motoneuron survival during this developmental period. Motoneuron cell death can also be observed in vitro when the motoneurons are isolated from the embryonic avian or rodent spinal cord. These isolated motoneurons and other types of primary neurons have been a useful tool for studying basic mechanisms underlying neuronal degeneration during development and under pathophysiological conditions in neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS). Accumulating evidence from such studies suggests that some specific requirements of motoneurons for survival and proper function may change during development. These findings might be relevant for understanding the patho-physiological processes underlying ALS and thus could contribute to the development of new therapeutic strategies.
机译:在高级脊椎动物的胚胎发育过程中,过量生成了动子素。在发育中的大鼠的腰脊髓中,在胚胎第14天时约有6000个运动神经元。这些神经元长出与它们的目标组织骨骼肌接触的轴突。从胚胎的第14天到出生后的第3天,在关键时期内约有50%的运动神经元丢失。这一过程被称为生理性运动神经元细胞死亡,一直是研究的重点,目的是确定在此期间调节运动神经元存活的神经营养因子。发展时期。当运动神经元从胚胎禽或啮齿动物脊髓中分离出来时,也可以在体外观察到动子神经细胞死亡。这些分离的运动神经元和其他类型的原代神经元已成为研究神经退行性疾病如肌萎缩性侧索硬化症(ALS)在发育过程中以及病理生理条件下神经元变性的基本机制的有用工具。这些研究的越来越多的证据表明,运动神经元对生存和正常功能的某些特定要求可能在发育过程中发生变化。这些发现可能与了解ALS的病理生理过程有关,因此可能有助于开发新的治疗策略。

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