通过MAPK级联触发局部能量赤字的病态轴突死亡
Jing Yang1, Zhuhao Wu1, Nicolas Renier1
1Laboratory of Brain Development and Repair, The Rockefeller University, New York, NY 10065, USA.
Cell
|January 17, 2015
概括
轴突退化是神经退行性疾病的标志,涉及一个新发现的Sarm1-MAPK通路,耗尽轴突能量. 诸如cytoNmnat1/Wld(s) 和AKT信号等保护性蛋白调节这种通路.
科学领域:
- 神经科学是一个神经科学.
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
背景情况:
- 轴突死亡损害神经回路连接,是神经退行性疾病的核心.
- 病理性轴突退化的机制,独立于编程细胞死亡,在很大程度上是未知的.
研究的目的:
- 在轴突损伤中调查基激活蛋白激酶 (MAPK) 家族.
- 确定早期轴突退化的反应中涉及的分子级联.
主要方法:
- 使用创伤性轴突损伤模型.
- 系统地研究了MAPK家族.
- 研究了Sarm1,cytoNmnat1/Wld(s),MKK4,AKT和JNK信号传递的作用.
主要成果:
- 确定了一种依赖于Sarm1的MAPK级联作为对轴突损伤的早期反应.
- 证明这种途径会破坏轴突能量恒温,导致ATP耗尽.
- 发现cytoNmnat1/Wld(s) 抑制了MAPK级联,而AKT信号则对抗MKK4以调节JNK信号.
结论:
- 揭示了一种整合Sarm1-MAPK,cytoNmnat1/Wld(s) 和AKT/JNK信号的调节机制,用于病理性轴突退化.
- 这条通路代表了受伤后轴突完整性的关键决定因素.
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