线粒体功能障碍加剧了综合应激反应,驱动ALS病变的发生
bioRxiv : the preprint server for biology
|May 27, 2024
概括
膀相关膜蛋白相关蛋白-B (VAPB) P56S突变通过破坏线粒体-ER接触和增加ER压力来损害运动神经元功能. 抑制综合应激反应 (ISR) 挽救了这些疾病表型,表明ALS的治疗标.
科学领域:
- 神经科学是一个神经科学.
- 细胞生物学 细胞生物学
- 遗传学 是一个遗传学.
背景情况:
- 肌缩侧面硬化症 (ALS) 是一种进展性神经退行性疾病.
- 囊泡相关膜蛋白相关蛋白-B (VAPB) 突变,特别是P56S,与家族性ALS有关.
- 通过VAPB突变引起运动神经元 (MN) 功能障碍的确切机制尚未完全理解.
结论:
- 通过神经元功能受损和ER压力,VAPB P56S突变有助于ALS的发病.
- 综合应激反应 (ISR) 途径在VAPB相关的ALS中发挥着关键作用.
- 阻断ISR代表了ALS患者具有VAPB突变的有前途的治疗策略.
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