失去心脏线粒体复合体I的化会损害老化中的NAD稳态
Maria-Kyriaki Drekolia1, Christina Karantanou1, Ilka Wittig2
1Department of Vascular Dysfunction, European Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany; Institute for Vascular Signalling, Centre for Molecular Medicine, Goethe University, Frankfurt Am Main, Germany.
Redox biology
|January 3, 2024
概括
蛋白质固硫化通过防止囊过氧化来保护心脏功能. 衰老减少了这种保护性修饰,损害了线粒体复合体I活动和心脏代谢.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 心血管科学 心血管科学
背景情况:
- 蛋白质固硫化是一种翻译后的修改,它可以保护囊氨酸残留物免受过度氧化.
- 这种修饰对于细胞功能至关重要,但随着年龄的增长而下降,特别是在心脏中.
研究的目的:
- 为了研究心脏蛋白质固硫化水平和衰老中的功能影响.
- 为了确定特定的化蛋白质及其在心脏代谢中的作用.
主要方法:
- 在野生类型和硫化物生成酶缺乏的小鼠 (CSE和3MST) 中分析心脏persulfydome.
- 专注于NDUFB7作为标蛋白,检查其固硫化和对线粒体复合体I活动的影响.
- 对心肌细胞中CSE,3MST和NDUFB7持续硫化发生与年龄相关的变化的评估.
主要成果:
- 心脏内硫化蛋白比其他器官少,主要参与线粒体代谢.
- 通过CSE和3MST进行NDUFB7硫化,可以防止过氧化,并维持线粒体复合体I活性.
- 衰老减少了CSE和3MST,导致NDUFB7硫化减少和心肌细胞中NADH/NAD+比率升高.
结论:
- 心脏内硫化直接与线粒体复合体I活动有关.
- 减少固硫化有助于与年龄相关的心脏功能和新陈代谢的下降.
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