Mesoporous silica nanoparticles trigger mitophagy in endothelial cells and perturb neuronal network activity in a size- and time-dependent manner

Autor: Maria Tringali, Francesca Gullo, Stefania Minniti, Ennio Tasciotti, Francesca Re, Andrea Becchetti, Antonina Orlando, Emanuela Cazzaniga, Francesca Taraballi
Přispěvatelé: Orlando, A, Cazzaniga, E, Tringali, M, Gullo, F, Becchetti, A, Minniti, S, Taraballi, F, Tasciotti, E, Re, F
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Mesoporous silica nanoparticle
Cell
Pharmaceutical Science
02 engineering and technology
chemistry.chemical_compound
Drug Delivery Systems
Endothelial cell
International Journal of Nanomedicine
Mitophagy
Drug Discovery
Original Research
Neurons
MEA
Brain
General Medicine
Silicon Dioxide
021001 nanoscience & nanotechnology
Enzymes
medicine.anatomical_structure
Drug delivery
Toxicity
Electrophoresis
Polyacrylamide Gel

0210 nano-technology
Materials science
Cell Survival
Biophysics
Nanotechnology
Bioengineering
Nitric Oxide
Cell Line
Nitric oxide
Biomaterials
03 medical and health sciences
Autophagy
Human Umbilical Vein Endothelial Cells
medicine
Humans
Nanotoxicity
Viability assay
mesoporous silica nanoparticles
Dose-Response Relationship
Drug

Cell Membrane
Organic Chemistry
Endothelial Cells
Neuron
Biomaterial
In vitro
030104 developmental biology
chemistry
Biophysic
Nanotoxicology
Nanoparticles
Zdroj: International Journal of Nanomedicine
Popis: Antonina Orlando,1 Emanuela Cazzaniga,1 Maria Tringali,2 Francesca Gullo,3 Andrea Becchetti,3 Stefania Minniti,1 Francesca Taraballi,4,5 Ennio Tasciotti,4,5 Francesca Re1 1Nanomedicine Center, School of Medicine and Surgery, University of Milano-Bicocca, Monza, 2Department of Environmental Sciences, 3Department of Biotechnologies and Biosciences, University of Milano-Bicocca, Milan, Italy; 4Center for Biomimetic Medicine, Houston Methodist Research Institute (HMRI), 5Department of Orthopedics and Sports Medicine, Houston Methodist Hospital, Houston, TX, USA Purpose: Mesoporous silica nanoparticles (MSNPs) are excellent candidates for biomedical applications and drug delivery to different human body areas, the brain included. Although toxicity at cellular level has been investigated, we are still far from using MSNPs in the clinic, because the mechanisms involved in the cellular responses activated by MSNPs have not yet been elucidated.Materials and methods: This study used an in vitro multiparametric approach to clarify relationships among size, dose, and time of exposure of MSNPs (0.05–1 mg/mL dose range), and cellular responses by analyzing the morphology, viability, and functionality of human vascular endothelial cells and neurons.Results: The results showed that 24 hours of exposure of endothelial cells to 250 nm MSNPs exerted higher toxicity in terms of mitochondrial activity and membrane integrity than 30 nm MSN at the same dose. This was due to induced cell autophagy (in particular mitophagy), probably consequent to MSNP cellular uptake (>20%). Interestingly, after 24 hours of treatment with 30 nm MSNPs, very low MSNP uptake (
Databáze: OpenAIRE