轴突
再生(生物学)
神经科学
生物
基因沉默
钙通道
轴突切开术
转录组
轴突引导
脊髓损伤
电压依赖性钙通道
脊髓
细胞生物学
钙
基因
医学
基因表达
遗传学
内科学
作者
Andrea Tedeschi,Sebastián Dupraz,Claudia J. Laskowski,Jia Xue,Thomas Ulas,Marc Beyer,Joachim L. Schultze,Frank Bradke
出处
期刊:Neuron
[Cell Press]
日期:2016-10-01
卷期号:92 (2): 419-434
被引量:265
标识
DOI:10.1016/j.neuron.2016.09.026
摘要
Injuries to the adult CNS often result in permanent disabilities because neurons lose the ability to regenerate their axon during development. Here, whole transcriptome sequencing and bioinformatics analysis followed by gain- and loss-of-function experiments identified Cacna2d2, the gene encoding the Alpha2delta2 subunit of voltage-gated calcium channels (VGCCs), as a developmental switch that limits axon growth and regeneration. Cacna2d2 gene deletion or silencing promoted axon growth in vitro. In vivo, Alpha2delta2 pharmacological blockade through Pregabalin (PGB) administration enhanced axon regeneration in adult mice after spinal cord injury (SCI). As PGB is already an established treatment for a wide range of neurological disorders, our findings suggest that targeting Alpha2delta2 may be a novel treatment strategy to promote structural plasticity and regeneration following CNS trauma.
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