高尿酸血症通过抑制有丝分裂促进尿酸引起的血管内皮细胞损伤

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Gang Wu, Jun Liu, Guirong Ma, Qiuyu Wei, Xinghui Song
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引用次数: 0

摘要

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)暴露于不同浓度的尿酸(6 mg/dL 至 50 mg/dL)中 48 小时,或暴露于 50 mg/dL 尿酸中不同时间点(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,尤其是在 40 毫克/分升和 50 毫克/分升 UA 浓度下。UA 处理后,自噬标记物 LC3 的荧光强度降低,LC3-II/LC3I、beclin1 和 p62 的表达减少,表明自噬功能受损。机理研究发现,HCQ 与线粒体自噬抑制剂环孢素 A(CsA)结合使用,会加剧 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到抑制,细胞衰老和凋亡加速。相反,线粒体自噬诱导剂羰基氰化间氯苯肼(CCCP)和 HCQ 的联合处理减轻了 UA 对 HUVEC 自噬的不利影响。这种干预导致 PINK1、Parkin、Bnip3 和 Nix 的表达增加,LC3-II/LC3-I 和 Parkin 的荧光增强,在促进细胞增殖的同时有效抑制了细胞衰老和凋亡。总之,我们的研究结果强调了 HCQ 在通过抑制有丝分裂调节 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潜力提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyperuricemia Facilitates Uric Acid-Mediated Vascular Endothelial Cell Damage by Inhibiting Mitophagy.

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.

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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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