血管生长素
蛋白激酶B
SOD1
肌萎缩侧索硬化
细胞生物学
生物
PI3K/AKT/mTOR通路
程序性细胞死亡
内质网
癌症研究
磷酸化
血管生成
信号转导
内科学
医学
细胞凋亡
生物化学
疾病
作者
Dairín Kieran,Jordi Sebastià,Matthew Greenway,Matthew King,Dervla M. Connaughton,Caoimhín G. Concannon,Beau J. Fenner,Orla Hardiman,Jochen H.M. Prehn
标识
DOI:10.1523/jneurosci.3399-08.2008
摘要
Mutations in the hypoxia-inducible factor angiogenin ( ANG ) have been identified in Amyotrophic Lateral Sclerosis (ALS) patients, but the potential role of ANG in ALS pathogenesis was undetermined. Here we show that angiogenin promotes motoneuron survival both in vitro and in vivo . Angiogenin protected cultured motoneurons against excitotoxic injury in a PI-3-kinase/Akt kinase-dependent manner, whereas knock-down of angiogenin potentiated excitotoxic motoneuron death. Expression of wild-type ANG protected against endoplasmic reticulum (ER) stress-induced and trophic-factor-withdrawal-induced cell death in vitro , whereas the ALS-associated ANG mutant K40I exerted no protective activity and failed to activate Akt-1. In SOD1 G93A mice angiogenin delivery increased lifespan and motoneuron survival, restored the disease-associated decrease in Akt-1 survival signaling, and reversed a pathophysiological increase in ICAM-1 expression. Our data demonstrate that angiogenin is a key factor in the control of motoneuron survival.
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