Acute, sub-chronic and chronic exposures to TiO and Ag nanoparticles differentially affects neuronal function in vitro.
Gerber, Lora-Sophie Heusinkveld, Harm J Langendoen, Celine Stahlmecke, Burkhard Schins, Roel Pf Westerink, Remco Hs
Gerber, Lora-Sophie
Heusinkveld, Harm J
Langendoen, Celine
Stahlmecke, Burkhard
Schins, Roel Pf
Westerink, Remco Hs
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Open Access
Type
Article
Language
en
Date of publication
2022-10-22
Year of publication
Research Projects
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Journal Issue
Title
Acute, sub-chronic and chronic exposures to TiO and Ag nanoparticles differentially affects neuronal function in vitro.
Translated Title
Published in
Neurotoxicology 2022; 93: 311 – 323
Abstract
In vivo toxicokinetic studies provide evidence for the translocation and accumulation of nanoparticles (NP) in the brain, thereby causing concern for adverse health effects, particularly for effects following chronic exposure. To date, only few studies investigated the effects of NP exposure on neuronal function in vitro, primarily focusing on short-term effects. The aim of this study was therefore to investigate the effects of two common types of NP, titanium dioxide NP (TiO2NP) and silver NP (AgNP), on neuronal function following acute (0.5h), sub-chronic (24h and 48h) and chronic (14 days) exposure in vitro. Effects of NP exposure on intracellular calcium homeostasis, spontaneous neuronal (network) activity and neuronal network morphology were investigated in rat primary cortical cells using respectively, single-cell microscopy calcium imaging, micro-electrode array (MEA) recordings and immunohistochemistry. Our data demonstrate that high doses of AgNP (≥ 30µg/mL) decrease calcium influx after 24h exposure, although neuronal activity is not affected following acute and sub-chronic exposure. However, chronic exposure to non-cytotoxic doses of AgNP (1-10µg/mL) potently decreases spontaneous neuronal (network) activity, without affecting network morphology and viability. Exposure to higher doses (≥ 30µg/mL) affects network morphology and is also associated with cytotoxicity. In contrast, acute and sub-chronic exposure to TiO2NP is without effects, whereas chronic exposure only modestly reduces neuronal function without affecting morphology. Our combined findings indicate that TiO2NP exposure is of limited hazard for neuronal function whereas AgNP, in particularly during chronic exposure, has profound effects on neuronal (network) function and morphology.