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心肌代谢物-胱抑素C通过AMPK-HIF-1α-PFKFB3途径促进糖酵解以改善体外循环诱导的肺损伤。

MOTS-c Promotes Glycolysis via AMPK-HIF-1α-PFKFB3 Pathway to Ameliorate CPB-induced Lung Injury.

作者信息

Shen Zihao, Lu Peng, Jin Wanjun, Wen Ziang, Qi Yuanpu, Li Xiangyu, Chu Mingyu, Yao Xin, Wu Minchao, Wang Ao, Zhang Xiao, Wang Wei, Song Meijuan, Wang Xiaowei

机构信息

The First Affiliated Hospital With Nanjing Medical University, Nanjing, Jiangsu, China.

The First Affiliated Hospital with Nanjing Medical University, Department of Cardiovascular Surgery, Nanjing, Jiangsu, China.

出版信息

Am J Respir Cell Mol Biol. 2025 Mar 4. doi: 10.1165/rcmb.2024-0533OC.

Abstract

Cardiopulmonary bypass (CPB) is essential during cardiac surgeries but frequently leads to lung ischemia-reperfusion injury (LIRI), a significant contributor to postoperative complications. This study investigated the protective effects of MOTS-c, a mitochondrial-derived peptide, against LIRI-induced acute lung injury (ALI), emphasizing glycolytic reprogramming and ferroptosis in pulmonary microvascular endothelial cells (PMVECs). We hypothesized that MOTS-c exerts its protective effects by regulating glycolysis and suppressing ferroptosis via metabolic signaling pathways. We conducted a prospective, controlled trial involving 107 patients undergoing CPB, evaluating plasma concentrations of MOTS-c and inflammatory markers. MOTS-c levels were significantly reduced in patients with ALI. In vivo and in vitro experiments demonstrated that MOTS-c pretreatment alleviated LIRI by enhancing glycolytic flux, reducing oxidative stress, and suppressing ferroptosis in PMVECs. MOTS-c specially reinstated the expression of PFKFB3, an essential glycolytic enzyme, thus preserving cellular energy homeostasis and diminishing lipid peroxidation. The study further emphasized the involvement of the AMPK-HIF-1α signaling pathway in the protective benefits facilitated by MOTS-c. MOTS-c elevated phosphorylated AMPKα and HIF-1α expression, indicating a vital function for these pathways in enhancing glycolysis and antioxidant defenses. Genetic and pharmacological inhibition of PFKFB3 abrogated the protective effects of MOTS-c, thereby confirming the essential role of PFKFB3-mediated glycolysis in alleviating LIRI. Our research indicates that MOTS-c could serve as a potential therapeutic agent for the prevention or treatment of LIRI-induced ALI by enhancing glycolysis, suppressing ferroptosis, and activating the AMPK-HIF-1α pathway. Future study should explore the clinical application of MOTS-c, potentially improving outcomes for patients undergoing high-risk cardiac operations.

摘要

体外循环(CPB)在心脏手术中至关重要,但经常导致肺缺血再灌注损伤(LIRI),这是术后并发症的一个重要因素。本研究调查了线粒体衍生肽 MOTS-c 对 LIRI 诱导的急性肺损伤(ALI)的保护作用,重点关注肺微血管内皮细胞(PMVECs)中的糖酵解重编程和铁死亡。我们假设 MOTS-c 通过调节糖酵解和通过代谢信号通路抑制铁死亡来发挥其保护作用。我们进行了一项前瞻性对照试验,纳入了 107 例接受 CPB 的患者,评估了 MOTS-c 和炎症标志物的血浆浓度。ALI 患者的 MOTS-c 水平显著降低。体内和体外实验表明,MOTS-c 预处理通过增强糖酵解通量、降低氧化应激和抑制 PMVECs 中的铁死亡来减轻 LIRI。MOTS-c 特别恢复了关键糖酵解酶 PFKFB3 的表达,从而维持细胞能量稳态并减少脂质过氧化。该研究进一步强调了 AMPK-HIF-1α 信号通路在 MOTS-c 促进的保护作用中的参与。MOTS-c 提高了磷酸化 AMPKα 和 HIF-1α 的表达,表明这些通路在增强糖酵解和抗氧化防御方面具有重要作用。对 PFKFB3 的基因和药理学抑制消除了 MOTS-c 的保护作用,从而证实了 PFKFB3 介导的糖酵解在减轻 LIRI 中的重要作用。我们的研究表明,MOTS-c 可以作为一种潜在的治疗剂,通过增强糖酵解、抑制铁死亡和激活 AMPK-HIF-1α 通路来预防或治疗 LIRI 诱导的 ALI。未来的研究应探索 MOTS-c 的临床应用,可能改善接受高风险心脏手术患者的预后。

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