轴突
肌萎缩侧索硬化
神经科学
变性(医学)
运动神经元
轴突变性
类有机物
人诱导多能干细胞
诱导多能干细胞
神经元
生物
解剖
医学
病理
脊髓
疾病
胚胎干细胞
基因
生物化学
作者
Siu Yu A. Chow,Yui Nakanishi,Shohei Kaneda,Yoshiho Ikeuchi
出处
期刊:Methods in molecular biology
日期:2022-01-01
卷期号:: 89-97
被引量:1
标识
DOI:10.1007/978-1-0716-2409-8_6
摘要
Degeneration of axons is characteristic of many devastating diseases including amyotrophic lateral sclerosis (ALS). However, lack of an in vitro neuronal culture system that mimics damages on nerves and axonal tracts hampered development of effective treatments. Here, we describe a method to model degeneration of motor neuron axons using motor nerve organoids that are formed with human induced pluripotent stem cells. In this protocol, motor neuron axon degeneration can be rapidly induced with chemical damages. Neuroprotective effects of compounds can be examined using the degenerated axons. This motor neuron axon bundle degeneration model should facilitate future screening for drugs against diseases affecting axon fascicles.
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