Human 3D Cultures as Models for Evaluating Magnetic Nanoparticle CNS Cytotoxicity after Short- and Repeated Long-Term Exposure.
Uliana De SimoneMarianna RoccioLaura GribaldoArsenio SpinilloFrancesca CaloniTeresa CocciniPublished in: International journal of molecular sciences (2018)
Since nanoparticles (NPs) can translocate to the brain and impact the highly vulnerable central nervous system (CNS), novel in vitro tools for the assessment of NP-induced neurotoxicity are advocated. In this study, two types of CNS spheroids have been developed from human D384 astrocyte- and SH-SY5Y neuronal-like cells, and optimized in combination with standard assays (viability readout and cell morphology) to test neurotoxic effects caused by Fe₃O₄NPs, as NP-model, after short- (24–48 h; 1–100µg/ml) and long-term repeated exposure (30days; 0.1–25µg/ml). Short-term exposure of 3D-spheroids to Fe₃O₄NP induced cytotoxicity at 10 µg/mL in astrocytes and 25 µg/mL neurons. After long-term repeated dose regimen, spheroids showed concentration- and time-dependent cell mortality at 10 µg/mL for D384 and 0.5 µg/mL for SH-SY5Y, indicating a higher susceptibility of neurons than astrocytes. Both spheroid types displayed cell disaggregation after the first week of treatment at ≥0.1 µg/mL and becoming considerably evident at higher concentrations and over time. Recreating the 3D-spatial environment of the CNS allows cells to behave in vitro more closely to the in vivo situations, therefore providing a model that can be used as a stand-alone test or as a part of integrated testing strategies. These models could drive an improvement in the species-relevant predictivity of toxicity testing.
Keyphrases
- endothelial cells
- single cell
- blood brain barrier
- high glucose
- cell therapy
- diabetic rats
- induced apoptosis
- stem cells
- cardiovascular events
- randomized controlled trial
- oxidative stress
- type diabetes
- cerebral ischemia
- induced pluripotent stem cells
- brain injury
- drug induced
- high resolution
- signaling pathway
- mass spectrometry
- cell death
- subarachnoid hemorrhage
- resting state
- combination therapy
- simultaneous determination
- oxide nanoparticles