Department of Genetics, Washington University Medical School, St Louis, Missouri 63110, USA.
J Biol Chem. 2011 Aug 12;286(32):28011-8. doi: 10.1074/jbc.M111.250472. Epub 2011 Jun 17.
Axon degeneration is an active, evolutionarily conserved self-destruction program by which compromised axons fragment in response to varied insults. Unlike programmed cell death, axon degeneration is poorly understood. We have combined robotic liquid handling with automated microscopy and image analysis to create a robust screening platform to measure axon degeneration in mammalian primary neuronal cultures. Using this assay, we performed an unbiased screen of 480 bioactive compounds, identifying 11 that reproducibly delay fragmentation of severed axons in vitro, including two inhibitors of glycogen synthase kinase 3 and two inhibitors of IκB kinase. Knockdown of each of these targets by shRNA lentivirus also delays axon degeneration in vitro, further supporting their role in the axon degeneration program.
轴突变性是一种受进化保守的主动自我毁灭程序,受损的轴突在受到各种损伤时会发生片段化。与程序性细胞死亡不同,轴突变性的了解甚少。我们结合机器人液体处理与自动化显微镜和图像分析,创建了一个强大的筛选平台,以测量哺乳动物原代神经元培养物中的轴突变性。使用该测定法,我们对 480 种生物活性化合物进行了无偏筛选,鉴定出 11 种可重复延迟体外切割轴突的片段化的化合物,其中包括两种糖原合酶激酶 3 抑制剂和两种 IκB 激酶抑制剂。这些靶点的 shRNA 慢病毒敲低也延迟了体外轴突变性,进一步支持它们在轴突变性程序中的作用。