Comparative study of human neuronal and glial cell sensitivity for in vitro neurogenotoxicity testing

被引:13
作者
Laffon, Blanca [1 ]
Fernandez-Bertolez, Natalia [1 ]
Costa, Carla [2 ]
Pasaro, Eduardo [1 ]
Valdiglesias, Vanessa [1 ,2 ]
机构
[1] Univ A Coruna, DICOMOSA Grp, Dept Psychol, Area Psychobiol, La Coruna, Spain
[2] Univ Porto, Inst Saude Publ, EPIUnit, Rua Taipas 135, P-4050600 Porto, Portugal
关键词
A172; cells; Comet assay; Neurogenotoxicity; Micronucleus test; SH-SY5Y cells; gamma H2AX assay; TITANIUM-DIOXIDE NANOPARTICLES; DOUBLE-STRAND BREAKS; DNA-DAMAGE; MICRONUCLEUS TEST; GAMMA-H2AX FOCI; ASSAY; TOXICITY; PHOSPHORYLATION; NEUROTOXICITY; GRISEOFULVIN;
D O I
10.1016/j.fct.2017.02.005
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Cell cultures from neuronal and glial origin have proven to be powerful tools for elucidating cellular and molecular mechanisms of nervous system development and physiology, and as neurotoxicity models to evaluate in vitro the possible effects of chemicals. But cellular heterogeneity of nervous system is considerable and these cells have been shown to respond diversely to neurotoxic insults, leading to disparate results from different studies. To shed more light on suitability of cellular models of nervous origin for neurotoxicity screening, the objective of this study was to compare the sensitivity to genetic damage induction of two nervous cell lines. To this aim, neurons (SH-SY5Y) and glial (A172) cells were treated with differently-acting genotoxic agents (bleomycin, actinomycin-D, methyl methanesulfonate, mitomycin C, and griseofulvin). After discarding cytotoxicity, genotoxicity was evaluated by a battery of assays encompassing detection of different genetic lesions. Results obtained showed that glial cells are generally more resistant to genotoxic damage induced by clastogenic agents, but more sensitive to aneugenic effects. These results highlight the need of proper design of in vitro neurotoxicology studies, especially for neurogenotoxicity screening, emphasizing the importance of employing more than one nervous cell type for testing the potential toxicity of a particular exposure. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:120 / 128
页数:9
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