Qi Pingping, Zhang Wei, Gao Yang, Chen Shengkui, Jiang Minghe, He Rong, Chen Wenzhong, Wei Xiawei, Hu Bingquan, Xu Hao, Wu Minsheng, Tang Rong
The Second Affiliated Hospital of Guangxi Medical University Blood Transfusion Department, Nanning, 533000, Guangxi, People's Repulic of China.
The First Affiliated Hospital of Harbin Medical University, Harbin, 533000, Heilongjiang, People's Repulic of China.
J Cell Physiol. 2024 Dec;239(12):e31448. doi: 10.1002/jcp.31448. Epub 2024 Sep 22.
N6-methyladenosine (m6A) is known to be crucial in various biological processes, but its role in sepsis-induced circulatory and cardiac dysfunction is not well understood. Specifically, mitophagy, a specialized form of autophagy, is excessively activated during lipopolysaccharide (LPS)-induced myocardial injury. This study aimed to investigate the impact of LPS-induced endotoxemia on m6A-RNA methylation and its role in regulating mitophagy in sepsis-induced myocardial dysfunction. Our research demonstrated that FTO (fat mass and obesity-associated protein), an m6A demethylase, significantly affects abnormal m6A modification in the myocardium and cardiomyocytes following LPS treatment. In mice, cardiac dysfunction and cardiomyocyte apoptosis worsened after adeno-associated virus serotype 9 (AAV9)-mediated FTO knockdown. Further analyses to uncover the cellular mechanisms improving cardiac function showed that FTO reduced mitochondrial reactive oxygen species, restored both basal and maximal respiration, and preserved mitochondrial membrane potential. We revealed that FTO plays a critical role in activating mitophagy by targeting BNIP3. Additionally, the cardioprotective effects of AAV-FTO were significantly compromised by mdivi-1, a mitophagy inhibitor. Mechanistically, FTO interacted with BNIP3 transcripts and regulated their expression in an m6A-dependent manner. Following FTO silencing, BNIP3 transcripts with elevated m6A modification levels in their coding regions were bound by YTHDF2 (YT521-B homology m6A RNA-binding protein 2), leading to mRNA destabilization and decreased BNIP3 protein levels. These findings highlight the importance of FTO-dependent cardiac m6A methylation in regulating mitophagy and enhance our understanding of this critical interplay, which is essential for developing therapeutic strategies to protect cardiac mitochondrial function, alleviate cardiac dysfunction, and improve survival during sepsis.
已知N6-甲基腺苷(m6A)在各种生物学过程中至关重要,但其在脓毒症诱导的循环和心脏功能障碍中的作用尚不清楚。具体而言,线粒体自噬是自噬的一种特殊形式,在脂多糖(LPS)诱导的心肌损伤过程中会过度激活。本研究旨在探讨LPS诱导的内毒素血症对m6A-RNA甲基化的影响及其在脓毒症诱导的心肌功能障碍中调节线粒体自噬的作用。我们的研究表明,m6A去甲基化酶FTO(脂肪量和肥胖相关蛋白)显著影响LPS处理后心肌和心肌细胞中异常的m6A修饰。在小鼠中,腺相关病毒血清型9(AAV9)介导的FTO基因敲低后,心脏功能障碍和心肌细胞凋亡恶化。进一步分析揭示改善心脏功能的细胞机制表明,FTO减少了线粒体活性氧,恢复了基础呼吸和最大呼吸,并维持了线粒体膜电位。我们发现FTO通过靶向BNIP3在激活线粒体自噬中起关键作用。此外,线粒体自噬抑制剂mdivi-1显著削弱了AAV-FTO的心脏保护作用。机制上,FTO与BNIP3转录本相互作用,并以m6A依赖的方式调节其表达。FTO沉默后,编码区m6A修饰水平升高的BNIP3转录本被YTHDF2(YT521-B同源m6A RNA结合蛋白2)结合,导致mRNA不稳定和BNIP3蛋白水平降低。这些发现突出了FTO依赖的心脏m6A甲基化在调节线粒体自噬中的重要性,并加深了我们对这一关键相互作用的理解,这对于制定保护心脏线粒体功能、减轻心脏功能障碍和提高脓毒症期间生存率的治疗策略至关重要。