综合应激反应增强了波纳提尼布诱导的心脏毒性
Gege Yan1, Zhenbo Han1, Youjeong Kwon1
1Department of Pharmacology and Regenerative Medicine, University of Illinois College of Medicine, Chicago (G.Y., Z.H., Y.K., J.J., S.B.N., X.D., S.P., S.-G.O.).
Circulation research
|February 7, 2024
概括
波纳替尼因扰乱线粒体能量产生而引起心脏损伤,通过GCN2.2激活综合应激反应 (ISR). 抑制ISR可以防止这种心脏毒性,提供一种潜在的治疗策略.
科学领域:
- 心脏病学 心脏病学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 线粒体功能障碍是心力衰竭的一个关键因素.
- 线粒体能量生产和信号通路之间的相互作用尚未完全理解.
- 已知白血病药物波纳替尼 (Ponatinib) 通过线粒体功能障碍引起心脏毒性.
研究的目的:
- 研究综合应激反应 (ISR) 在波纳提尼布诱导的心脏毒性的作用.
- 阐明将线粒体压力与ISR激活由ponatinib联系起来的分子机制.
主要方法:
- 利用人类诱导的多能干细胞衍生的心肌细胞和小鼠模型.
- 进行蛋白质组分析,分子和生化分析.
- 研究了ISR抑制和NAD+前体补充剂的影响.
主要成果:
- 波纳替尼激活了心脏细胞中的ISR,GCN2被确定为关键激酶.
- 波纳替尼抑制了ATP合成酶,导致ATP缺乏,触发了ISR激活.
- 降低的ATP水平促进了ponatinib直接激活GCN2.
- 在小鼠中,ISR抑制保护了心肌细胞和减弱了心脏功能障碍,而不会影响ponatinib的抗瘤作用.
结论:
- 中和ISR过活化可以预防或逆转波纳替尼诱导的心脏毒性.
- 损害ATP生产会增强GCN2介导的ISR激活,这对各种心脏病有影响.
- 波纳替尼直接激活GCN2,独立于其ATP竞争性激酶抑制.
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