Cerium Oxide Nanoparticles Protect Endothelial Cells from Apoptosis Induced by Oxidative Stress

被引:114
作者
Chen, Shizhu [1 ]
Hou, Yingjian [2 ]
Cheng, Gong [1 ]
Zhang, Cuimiao [1 ]
Wang, Shuxiang [1 ]
Zhang, Jinchao [1 ]
机构
[1] Hebei Univ, Coll Chem & Environm Sci, Chem Biol Key Lab Hebei Prov, Baoding, Peoples R China
[2] Hebei Univ, Coll Basic Med, Baoding, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Nanoceria; Antioxidant; Endothelial cells; Apoptosis; MITOCHONDRIAL DEPOLARIZATION; TOXICITY; ROS; CYTOTOXICITY; STATE; ASSAY;
D O I
10.1007/s12011-013-9678-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxidative stress is well documented to cause injury to endothelial cells (ECs), which in turn trigger cardiovascular diseases. Previous studies revealed that cerium oxide nanoparticles (nanoceria) had antioxidant property, but the protective effect of nanoceria on ROS injury to ECs and cardiovascular diseases has not been reported. In the current study, we investigated the protective effect and underlying mechanisms of nanoceria on oxidative injury to ECs. The cell viability, lactate dehydrogenase release, cellular uptake, intracellular localization and reactive oxygen species (ROS) levels, endocytosis mechanism, cell apoptosis, and mitochondrial membrane potential were performed. The results indicated that nanoceria had no cytotoxicity on ECs but had the ability to prevent injury by H2O2. Nanoceria could be uptaken into ECs through caveolae- and clathrin-mediated endocytosis and distributed throughout the cytoplasma. The internalized nanoceria effectively attenuated ROS overproduction induced by H2O2. Apoptosis was also alleviated greatly by nanoceria pretreatment. These results may be helpful for more rational application of nanoceria in biomedical fields in the future.
引用
收藏
页码:156 / 166
页数:11
相关论文
共 50 条
[1]  
[Anonymous], 2011, WHO I Global atlas on cardiovascular disease prevention and control
[2]   Regulatory role of mitochondria in oxidative stress and atherosclerosis [J].
Chang, Jui-Chih ;
Kou, Shou-Jen ;
Lin, Wei-Ting ;
Liu, Chin-San .
WORLD JOURNAL OF CARDIOLOGY, 2010, 2 (06) :150-159
[3]   Free radical biology of the cardiovascular system [J].
Chen, Alex F. ;
Chen, Dan-Dan ;
Daiber, Andreas ;
Faraci, Frank M. ;
Li, Huige ;
Rembold, Christopher M. ;
Laher, Ismail .
CLINICAL SCIENCE, 2012, 123 (1-2) :73-91
[4]   Involvement of Kv1.5 Protein in Oxidative Vascular Endothelial Cell Injury [J].
Chen, Wen-Liang ;
Huang, Xiong-Qing ;
Zhao, Li-Yan ;
Li, Jie ;
Chen, Jian-Wen ;
Xiao, Ying ;
Huang, Yun-Ying ;
Liu, Jie ;
Wang, Guan-Lei ;
Guan, Yong-Yuan .
PLOS ONE, 2012, 7 (11)
[5]   Cerium oxide and platinum nanoparticles protect cells from oxidant-mediated apoptosis [J].
Clark, Andrea ;
Zhu, Aiping ;
Sun, Kai ;
Petty, Howard R. .
JOURNAL OF NANOPARTICLE RESEARCH, 2011, 13 (10) :5547-5555
[6]   Protection from radiation-induced pneumonitis using cerium oxide nanoparticles [J].
Colon, Jimmie ;
Herrera, Luis ;
Smith, Joshua ;
Patil, Swanand ;
Komanski, Chris ;
Kupelian, Patrick ;
Seal, Sudipta ;
Jenkins, D. Wayne ;
Baker, Cheryl H. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2009, 5 (02) :225-231
[7]   Auto-catalytic ceria nanoparticles offer neuroprotection to adult rat spinal cord neurons [J].
Das, Mainak ;
Patil, Swanand ;
Bhargava, Neelima ;
Kang, Jung-Fong ;
Riedel, Lisa M. ;
Seal, Sudipta ;
Hickman, James J. .
BIOMATERIALS, 2007, 28 (10) :1918-1925
[8]   Combating oxidative stress in vascular disease: NADPH oxidases as therapeutic targets [J].
Drummond, Grant R. ;
Selemidis, Stavros ;
Griendling, Kathy K. ;
Sobey, Christopher G. .
NATURE REVIEWS DRUG DISCOVERY, 2011, 10 (06) :453-471
[9]  
Eruslanov E, 2010, METHODS MOL BIOL, V594, P57, DOI 10.1007/978-1-60761-411-1_4
[10]  
Estevez AY, 2011, ACS SYM SER, V1083, P255