Wu Gang, Liu Jun, Ma Guirong, Wei Qiuyu, Song Xinghui
Department of institute office, Liuzhou Traditional Chinese Medicine Hospital, No. 32 Jiefang North Road, Chengzhong District, Liuzhou City, Guangxi Zhuang Autonomous Region, China.
Department of neurosurgery, Liuzhou People's Hospital, No. 8 Wenchang Road, Chengzhong District, Liuzhou City, Guangxi Zhuang Autonomous Region, China.
Cell Biochem Biophys. 2025 Mar;83(1):811-821. doi: 10.1007/s12013-024-01512-5. Epub 2024 Sep 28.
Hyperuricemia remains an elusive factor in the pathogenesis of vascular endothelial injury. This study elucidates the role of hydroxychloroquine (HCQ) in the context of uric acid (UA)-induced vascular endothelial cell damage. Human umbilical vein endothelial cells (HUVECs) were exposed to varying UA concentrations (6 mg/dL to 50 mg/dL) for 48 h, or to 50 mg/dL UA for different time points (6 to 72 h). We observed a concentration- and time-dependent inhibition of cell proliferation, particularly at 40 mg/dL and 50 mg/dL UA. The autophagy marker LC3 exhibited reduced fluorescence intensity post-UA treatment, along with decreased expression of LC3-II/LC3I, beclin1, and p62, indicating impaired autophagy. The mechanistic exploration revealed that HCQ, in conjunction with the mitochondrial autophagy inhibitor Cyclosporine A (CsA), exacerbated the inhibitory effects of UA on HUVEC autophagy. This was evidenced by a further reduction in mitochondrial autophagy-related proteins and diminished fluorescence of LC3-II/LC3-I and Parkin, culminating in suppressed cell proliferation and accelerated cell senescence and apoptosis. Conversely, the co-treatment with the mitochondrial autophagy inducer carbonyl cyanide m-chlorophenyl hydrazine (CCCP) and HCQ mitigated the detrimental effects of UA on HUVEC autophagy. This intervention led to increased expression of PINK1, Parkin, Bnip3, and Nix, along with enhanced fluorescence of LC3-II/LC3-I and Parkin, effectively inhibiting cell senescence and apoptosis while promoting cell proliferation. In conclusion, our findings underscore the pivotal role of HCQ in modulating UA-mediated vascular endothelial cell damage through the inhibition of mitophagy, providing novel insights into the therapeutic potential of targeting HCQ in the management of hyperuricemia-associated vascular complications.
高尿酸血症仍然是血管内皮损伤发病机制中一个难以捉摸的因素。本研究阐明了羟氯喹(HCQ)在尿酸(UA)诱导的血管内皮细胞损伤中的作用。将人脐静脉内皮细胞(HUVECs)暴露于不同浓度的UA(6mg/dL至50mg/dL)中48小时,或暴露于50mg/dL的UA中不同时间点(6至72小时)。我们观察到细胞增殖受到浓度和时间依赖性抑制,特别是在40mg/dL和50mg/dL的UA浓度下。自噬标志物LC3在UA处理后荧光强度降低,并伴有LC3-II/LC3I、beclin1和p62表达减少,表明自噬受损。机制探索表明,HCQ与线粒体自噬抑制剂环孢素A(CsA)联合使用,加剧了UA对HUVEC自噬的抑制作用。这表现为线粒体自噬相关蛋白进一步减少,LC3-II/LC3-I和Parkin的荧光减弱,最终导致细胞增殖受抑制、细胞衰老和凋亡加速。相反,线粒体自噬诱导剂间氯苯腙(CCCP)与HCQ联合处理减轻了UA对HUVEC自噬的有害影响。这种干预导致PINK1、Parkin、Bnip3和Nix表达增加,同时LC3-II/LC3-I和Parkin的荧光增强,有效抑制细胞衰老和凋亡,同时促进细胞增殖。总之,我们的研究结果强调了HCQ通过抑制线粒体自噬在调节UA介导的血管内皮细胞损伤中的关键作用,为靶向HCQ治疗高尿酸血症相关血管并发症的治疗潜力提供了新的见解。