Platinum Nanoparticle-Based Microreactors as Support for Neuroblastoma Cells

被引:26
作者
Armada-Moreira, Ana [1 ,2 ,3 ]
Taipaleenmaki, Essi [1 ]
Baekgaard-Laursen, Marie [1 ]
Schattling, Philipp Sebastian [1 ]
Sebastiao, Ana M. [2 ,3 ]
Vaz, Sandra H. [2 ,3 ]
Stadler, Brigitte [1 ]
机构
[1] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, Gustav Wieds Vej 14, DK-8000 Aarhus, Denmark
[2] Univ Lisbon, Fac Med, Inst Farmacol & Neurociencias, P-1649028 Lisbon, Portugal
[3] Univ Lisbon, Fac Med, Inst Med Mol, P-1649028 Lisbon, Portugal
基金
欧盟地平线“2020”;
关键词
Polydopamine; neuroblastoma cells; excitotoxicity; oxidative stress; ammonia toxicity; platinum nanoparticles; NITRIC-OXIDE; HYDROGEN-PEROXIDE; OXIDATIVE STRESS; MOLECULAR-MECHANISMS; POLYDOPAMINE; GLUTAMATE; AMMONIA; EXCITOTOXICITY; BRAIN; TOXICITY;
D O I
10.1021/acsami.7b10724
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Excitotoxicity is a common phenomenon in several neurological diseases, associated with an impaired clearance of synaptically released glutamate, which leads to an overactivation of postsynaptic glutamate receptors. This will, in turn, start an intracellular cascade of neurotoxic events, which include exacerbated production of reactive oxygen species and ammonia toxicity. We report the assembly of microreactors equipped with platinum nanoparticles as artificial enzymes and polymer terminating layers including poly(dopamine). The biological response to these microreactors is assessed in human neuroblastoma cell culture. The microreactors' function to deplete hydrogen peroxide (H2O2) and ammonia is confirmed. While the proliferation of the cells depends on the number of microreactors present, no inherent toxicity is found. Furthermore, the microreactors are able to ameliorate the effects of excitotoxicity in cell culture by scavenging H2O2 and ammonia, thus having the potential to provide a therapeutic approach for several neurological diseases in which excitotoxicity is observed.
引用
收藏
页码:7581 / 7592
页数:12
相关论文
共 70 条
[1]   7-Nitroindazole, a neuronal nitric oxide synthase inhibitor, impairs passive-avoidance and elevated plus-maze memory performance in rats [J].
Akar, Furuzan Yildiz ;
Ulak, Guner ;
Tanyeri, Pelin ;
Erden, Faruk ;
Utkan, Tijen ;
Gacar, Nejat .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2007, 87 (04) :434-443
[2]   Droplet-microfluidics towards the assembly of advanced building blocks in cell mimicry [J].
Armada-Moreira, Ana ;
Taipaleenmaki, Essi ;
Itel, Fabian ;
Zhang, Yan ;
Stadler, Brigitte .
NANOSCALE, 2016, 8 (47) :19510-19522
[3]   The glutamate/GABA-glutamine cycle: aspects of transport, neurotransmitter homeostasis and ammonia transfer [J].
Bak, Lasse K. ;
Schousboe, Arne ;
Waagepetersen, Helle S. .
JOURNAL OF NEUROCHEMISTRY, 2006, 98 (03) :641-653
[4]   Enhanced neuronal differentiation of pheochromocytoma 12 cells on polydopamine-modified surface [J].
Bhang, Suk Ho ;
Kwon, Sun-Hyun ;
Lee, Seahyoung ;
Kim, Gui Chul ;
Han, Ah Mi ;
Kwon, Yun Hee Kim ;
Kim, Byung-Soo .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 430 (04) :1294-1300
[5]   Multifunctional platinum-based nanoparticles for biomedical applications [J].
Cheng, Qinqin ;
Liu, Yangzhong .
WILEY INTERDISCIPLINARY REVIEWS-NANOMEDICINE AND NANOBIOTECHNOLOGY, 2017, 9 (02)
[6]   The metabolic response to excitotoxicity - lessons from single-cell imaging [J].
Connolly, Niamh M. C. ;
Prehn, Jochen H. M. .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2015, 47 (1-2) :75-88
[7]   OXIDATIVE STRESS, GLUTAMATE, AND NEURODEGENERATIVE DISORDERS [J].
COYLE, JT ;
PUTTFARCKEN, P .
SCIENCE, 1993, 262 (5134) :689-695
[8]  
DAWSON VL, 1993, J NEUROSCI, V13, P2651
[9]   Nitric oxide neurotoxicity [J].
Dawson, VL ;
Dawson, TM .
JOURNAL OF CHEMICAL NEUROANATOMY, 1996, 10 (3-4) :179-190
[10]   A QUICK AND SIMPLE METHOD FOR THE QUANTITATION OF LACTATE-DEHYDROGENASE RELEASE IN MEASUREMENTS OF CELLULAR CYTO-TOXICITY AND TUMOR NECROSIS FACTOR (TNF) ACTIVITY [J].
DECKER, T ;
LOHMANNMATTHES, ML .
JOURNAL OF IMMUNOLOGICAL METHODS, 1988, 115 (01) :61-69