首页|MoS2纳米酶通过调控线粒体动力及自噬减轻炎性内皮细胞损伤

MoS2纳米酶通过调控线粒体动力及自噬减轻炎性内皮细胞损伤

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探讨新型MoS2纳米酶通过调控线粒体动力,以减轻炎性血管内皮细胞损伤的保护机制.利用水热法制备出了花状MoS2纳米片,结合电子自旋共振(electron spin resonance,ESR)光谱检测技术,表明花状MoS2纳米片对羟基自由基(·OH)和单线态氧(1O2)都具有很强的清除能力,呈剂量依赖效应.通过体外脂多糖(lipopolysaccharide,LPS)诱导的血管内皮细胞炎性氧化应激损伤模型,用花状MoS2纳米片预处理,本研究分别用MTT及Annexin V-FITC/PI双染法检测内皮细胞毒性及凋亡;用MitoTracker荧光探针观察内皮细胞线粒体分裂及融合形态;用活性氧(reactive oxygen species,ROS)探针DCFH-DA及超氧阴离子(O2)探针DHE检测细胞氧化应激水平;用质粒GFP-LC3转染及荧光共定位技术观察并分析细胞自噬及线粒体自噬形成.结果表明,MoS2纳米酶可以显著减少炎性内皮细胞的细胞毒性及细胞凋亡,减轻炎性内皮细胞线粒体的分裂,并维持融合状态下的线粒体动力;还可以缓解LPS介导的内皮细胞线粒体自噬,进而保护内皮细胞免受炎性氧化应激性损伤.以上结果确立了新型MoS2纳米酶可以通过调控内皮细胞线粒体动力及线粒体自噬,实现对炎性内皮细胞损伤的保护,有望拓展MoS2纳米酶用于防治慢性炎症性血管内皮损伤相关疾病.
MoS2 nanozyme attenuated inflammation-related endothelial cell injury by regulating mitochondrial dynamics and mitophagy
To explore the protective mechanisms of a novel molybdenum disulfide(MoS2)nanozyme in alleviating inflammation-related endothelial cell injury by regulating mitochondrial dynamic,flower like-MoS2 nanosheets were prepared by hydrothermal method,and its antioxidant enzyme-mimic activities were assessed via electron spin resonance(ESR)spectroscopy.It was shown that MoS2 nanosheets had strong scavenging ability for hydroxyl radical(·OH)and singlet reactive oxygen species(1O2)in a dose-dependent manner.Using an in vitro lipopolysaccharide(LPS)-induced vascular endothelial cell injury model,the protective roles of MoS2 nanozyme on cytotoxicity and apoptosis of endothelial cells were examined by MTT and Annexin V-FITC/PI assay,respectively.Mitochondrial fission/fusion of endothelial cell were observed by Mito-Tracker green probe.Reactive oxygen species(ROS)probe DCFH-DA and superoxide anion probe DHE were used to detect the level of oxidative stress in vitro.Plasmid GFP-LC3 transfection using colocalization analysis was applied to assess the autophagy of endothelial cells.The results showed that MoS2 nanozyme could significantly reduce the cytotoxicity and apoptosis of endothelial cells stimulated by LPS,and prevent the impairment mitochondrial dynamics of endothelial cells,thus maintaining mitochondrial dynamics.In addition,MoS2 nanozyme was also shown to alleviate LPS-mediated endothelial mitochondrial autophagy,thus protecting endothelial cells from inflammatory stress.These results established that MoS2 nanozyme protected endothelial cells injury from inflammatory stress by regulating mitochondrial dynamics and mitochondrial autophagy of endothelial cells,which is expected to expand the use of MoS2 nanozyme in the prevention and treatment of inflammation-related vascular endothelial diseases.

MoS2 nanozymevascular endotheliumoxidative stressmitochondrial dynamicsmitophagy

潘冬梅、柯孙葵、尹乾浩、杨沛彦、李超、叶社房

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厦门医学院附属海沧医院,福建厦门 361000

厦门大学附属中山医院,福建厦门 361004

厦门大学材料学院,生物材料系/生物医学工程研究中心/福建省高校重点实验室,厦门市生物医学工程技术研究中心,福建厦门 361005

厦门大学附属第一医院,福建厦门 361004

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MoS2纳米酶 血管内皮 氧化应激 线粒体动力 线粒体自噬

国家自然科学基金面上资助项目国家自然科学基金面上资助项目厦门市自然科学基金项目

32071396820734053502Z20227425

2024

药学学报
中国药学会 中国医学科学院药物研究所

药学学报

CSTPCD北大核心
影响因子:1.274
ISSN:0513-4870
年,卷(期):2024.59(10)