Luo Xing, Li Ji, Chen Yuwu, Weng Xiuzhu, Bao Xiaoyi, Bai Xiaoxuan, Lv Ying, Zhang Shan, Zhu Xinxin, Xu Biyi, Zhao Chen, Zeng Ming, Wu Tianyu, Sun Qianhui, Wang Shengfang, Liu Minghao, Johnson Thomas, White Stephen J, Libby Peter, Hu Sining, Yu Bo, Jia Haibo
Department of Cardiology of the Second Affiliated Hospital, Harbin Medical University, State Key Laboratory of Frigid Zone Cardiovascular Diseases (SKLFZCD), Nangang District, Harbin, China; Key Laboratory of Myocardial Ischemia, Ministry of Education, Nangang District, Harbin, China.
Department of Cardiology, Bristol Heart Institute, Bristol, United Kingdom.
JACC Basic Transl Sci. 2025 Aug;10(8):101283. doi: 10.1016/j.jacbts.2025.03.015.
Smoking is the only cardiovascular risk factor for plaque erosion. We found cigarette tar resulted in erosion-like lesion development in apolipoprotein E mice, with mural thrombosis, discontinuous endothelium, platelet activation, smooth muscle cell proliferation, and hyaluronic acid accumulation in the aorta. Single-cell transcriptomics revealed that genes relating to pyroptosis, platelet activation, and leukocytes adhesion were significantly increased in an endothelial cell subset. Rescue assays indicated cigarette tar caused human coronary artery endothelial cell pyroptosis by enhanced calcium-calmodulin-dependent protein kinase II / dynamin-related protein 1-mediated mitochondrial fission and mitochondrial DNA release via activating Ca signaling. Inhibition of endothelial cell pyroptosis may be a novel therapeutic strategy to reduce plaque erosion.
吸烟是斑块侵蚀的唯一心血管危险因素。我们发现香烟焦油可导致载脂蛋白E小鼠出现类似侵蚀的病变,伴有主动脉壁血栓形成、内皮不连续、血小板活化、平滑肌细胞增殖和透明质酸积聚。单细胞转录组学显示,在内皮细胞亚群中,与细胞焦亡、血小板活化和白细胞黏附相关的基因显著增加。挽救实验表明,香烟焦油通过激活钙信号,增强钙调蛋白依赖性蛋白激酶II/动力相关蛋白1介导的线粒体分裂和线粒体DNA释放,从而导致人冠状动脉内皮细胞焦亡。抑制内皮细胞焦亡可能是减少斑块侵蚀的一种新的治疗策略。