Inhibition of heterogeneous nuclear ribonucleoproteins A1 and oxidative stress reduces glycolysis via pyruvate kinase M2 in chronic thromboembolic pulmonary hypertension.

IF 1.4 3区 社会学 Q2 INTERNATIONAL RELATIONS Alternatives Pub Date : 2023-03-19 eCollection Date: 2024-09-01 DOI:10.2478/jtim-2022-0051
Lianhua Liu, Wenyi Pang, Jixiang Liu, Shiqing Xu, Zhu Zhang, Risheng Hao, Jun Wan, Wanmu Xie, Xincao Tao, Peiran Yang, Lan Zhao, Zhenguo Zhai, Chen Wang
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Abstract

Background and objective: Chronic thromboembolic pulmonary hypertension (CTEPH) is a lethal complication of pulmonary embolism involving pulmonary artery occlusion and microvascular disease. The glucose metabolism and reactive oxygen species (ROS) production may be perturbed in CTEPH, but the precise mechanisms are unclear. This study investigated glucose metabolism in CTEPH employing pulmonary endarterectomy (PEA)-derived pulmonary artery smooth muscle cells (PASMCs) and characterized the roles of pyruvate kinase M2 (PKM2) and its regulation by heterogeneous nuclear ribonucleoproteins A1 (hnRNPA1) and ROS in CTEPH.

Methods: PEA tissues and blood samples of CTEPH patients were collected to study the levels of PKM2. Primary PASMCs were isolated from PEA tissues. We used small interfering RNAs to knock down PKM2 and hnRNPAI, and applied antioxidant N-acetylcysteine (NAC) and mito-TEMPO to reduce ROS production. The expression of glucometabolic genes, ROS production, glycolysis rate and proliferative and migratory activities were analyzed in PEA-derived PASMCs.

Results: PKM2 levels in serum and PEA tissues of CTEPH patients were higher than that of the healthy controls. Compared to the control PASMCs, PEA-derived PASMCs showed increased PKM2 expression and ROS production. The rates of glycolysis, proliferation and migration were increased in PEA-PASMCs and could be mitigated by PKM2 downregulation through hnRNPA1 or ROS inhibition.

Conclusions: Increased glycolysis and PKM2 expression were found in PEA-PASMCs. Inhibition of hnRNPA1 or ROS corrected the aberrant glycolysis, cell proliferation and migration by downregulating PKM2. Regulation of the hnRNPA1/PKM2 axis represents a potential therapeutic target for the treatment of CTEPH.

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抑制异质核糖核蛋白 A1 和氧化应激可通过丙酮酸激酶 M2 减少慢性血栓栓塞性肺动脉高压中的糖酵解。
背景和目的:慢性血栓栓塞性肺动脉高压(CTEPH)是肺栓塞的一种致命并发症,涉及肺动脉闭塞和微血管病变。CTEPH 的糖代谢和活性氧(ROS)生成可能受到干扰,但其确切机制尚不清楚。本研究利用肺动脉内膜切除术(PEA)产生的肺动脉平滑肌细胞(PASMCs)研究了CTEPH中的糖代谢,并探讨了丙酮酸激酶M2(PKM2)及其受异质核核糖核蛋白A1(hnRNPA1)和ROS调控在CTEPH中的作用:收集 CTEPH 患者的 PEA 组织和血液样本以研究 PKM2 的水平。从 PEA 组织中分离出原发性 PASMCs。我们使用小干扰 RNA 敲除 PKM2 和 hnRNPAI,并使用抗氧化剂 N-乙酰半胱氨酸(NAC)和 mito-TEMPO 减少 ROS 的产生。分析了PEA衍生的PASMC中糖代谢基因的表达、ROS的产生、糖酵解率以及增殖和迁移活性:结果:CTEPH 患者血清和 PEA 组织中的 PKM2 水平高于健康对照组。与对照组 PASMCs 相比,PEA 衍生的 PASMCs 显示 PKM2 表达和 ROS 生成增加。PEA-PASMCs的糖酵解率、增殖率和迁移率增加,而通过hnRNPA1或ROS抑制剂下调PKM2可以缓解这种情况:结论:PEA-PASMCs中糖酵解和PKM2表达增加。抑制 hnRNPA1 或 ROS 可通过下调 PKM2 纠正糖酵解异常、细胞增殖和迁移。调节 hnRNPA1/PKM2 轴是治疗 CTEPH 的潜在治疗靶点。
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来源期刊
Alternatives
Alternatives INTERNATIONAL RELATIONS-
CiteScore
2.30
自引率
15.40%
发文量
19
期刊介绍: A peer-reviewed journal, Alternatives explores the possibilities of new forms of political practice and identity under increasingly global conditions. Specifically, the editors focus on the changing relationships between local political practices and identities and emerging forms of global economy, culture, and polity. Published in association with the Center for the Study of Developing Societies (India).
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