Liu Haodong, Peng Chunting, Su Qisheng, Liang Shijie, Qiu Yuling, Mo Wuning, Yang Zheng
Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, China.
Ann Hematol. 2025 Apr;104(4):2207-2219. doi: 10.1007/s00277-025-06359-1. Epub 2025 Apr 17.
Hemoglobin H Disease-Constant Spring (HbH-CS) represents a severe variant of α-thalassemia characterized by a fundamental pathological mechanism involving inadequate synthesis of α-globin chains. This deficiency results in the formation of unstable Hemoglobin H (HbH) due to the aggregation of free β-globin chains, which subsequently induces an imbalance in oxidative stress within erythrocytes. This imbalance leads to an abnormal accumulation of reactive oxygen species (ROS), which in turn promotes lipid peroxidation, culminating in the production of malondialdehyde (MDA) and a significant depletion of glutathione (GSH). Concurrently, Nrf2 is translocated to the nucleus, where it activates the antioxidant response element (ARE) to mitigate cellular stress. Here, we report that NSUN3 (which, together with ALKBH1, maintains mitochondrial function through m5C→f5C modification) is abnormally overexpressed in reticulocytes from patients with HbH-CS, and an in vitro cellular model of NSUN3 overexpression/silencing was constructed using K562 cells, which have the potential for erythroid lineage differentiation and retain an intact cluster of bead protein genes. Functional assays indicated that the overexpression of NSUN3 significantly intensified the accumulation of intracellular ROS and MDA, led to a reduction in GSH levels, and diminished the overall cellular antioxidant capacity (T-AOC). This may be due to ROS accumulation resulting from inhibition of mitochondrial respiratory chain complex I, II, and IV synthesis through aberrant m5C→f5C modification. In addition, NSUN3 overexpression further exacerbates oxidative stress by inhibiting the phosphorylation of Nrf2 hindering its translocation into the nucleus and weakening the cellular antioxidant system. Moreover, we also observed that NSUN3 overexpression exacerbated intracellular DNA damage and inhibited cellular value-added activity, and silencing NSUN3 showed the opposite result. Our research offers initial insights into the molecular mechanisms through which NSUN3 modulates oxidative stress in erythrocytes via its role in epigenetic modifications. These findings contribute to a deeper understanding of the clinical management of patients with Hb H-CS.
血红蛋白H病-Constant Spring(HbH-CS)是α地中海贫血的一种严重变体,其基本病理机制是α珠蛋白链合成不足。这种缺陷导致游离β珠蛋白链聚集,形成不稳定的血红蛋白H(HbH),进而引起红细胞内氧化应激失衡。这种失衡导致活性氧(ROS)异常积累,进而促进脂质过氧化,最终产生丙二醛(MDA)并导致谷胱甘肽(GSH)显著消耗。同时,Nrf2易位至细胞核,在那里它激活抗氧化反应元件(ARE)以减轻细胞应激。在此,我们报告NSUN3(与ALKBH1一起通过m5C→f5C修饰维持线粒体功能)在HbH-CS患者的网织红细胞中异常过表达,并使用具有红系分化潜能且保留完整珠蛋白基因簇的K562细胞构建了NSUN3过表达/沉默的体外细胞模型。功能测定表明,NSUN3的过表达显著增强了细胞内ROS和MDA的积累,导致GSH水平降低,并降低了整体细胞抗氧化能力(T-AOC)。这可能是由于异常的m5C→f5C修饰抑制线粒体呼吸链复合体I、II和IV的合成导致ROS积累。此外,NSUN3过表达通过抑制Nrf2的磷酸化,阻碍其易位至细胞核并削弱细胞抗氧化系统,进一步加剧氧化应激。此外,我们还观察到NSUN3过表达加剧了细胞内DNA损伤并抑制细胞增殖活性,而沉默NSUN3则产生相反的结果。我们的研究初步揭示了NSUN3通过其在表观遗传修饰中的作用调节红细胞氧化应激的分子机制。这些发现有助于更深入地理解Hb H-CS患者的临床管理。