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dc.contributor.authorLaffon, Blanca
dc.contributor.authorFernández-Bertólez, Natalia
dc.contributor.authorCosta, C.
dc.contributor.authorPásaro, Eduardo
dc.contributor.authorValdiglesias, Vanessa
dc.date.accessioned2024-11-04T19:28:58Z
dc.date.available2024-11-04T19:28:58Z
dc.date.issued2017-02-03
dc.identifier.citationLaffon, B., Fernández-Bertólez, N., Costa, C., Pásaro, E., Valdiglesias, V., 2017. Comparative study of human neuronal and glial cell sensitivity for in vitro neurogenotoxicity testing. Food and Chemical Toxicology 102, 120–128. https://doi.org/10.1016/j.fct.2017.02.005es_ES
dc.identifier.issn0278-6915
dc.identifier.urihttp://hdl.handle.net/2183/39930
dc.descriptionThis is an accepted version of the published document.es_ES
dc.description.abstract[Abstract] 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.es_ES
dc.description.sponsorshipResearch funded by Xunta de Galicia (ED431B 2016/013). V. Valdiglesias was supported by a Xunta de Galicia postdoctoral fellowship (reference ED481B 2016/190-0)es_ES
dc.description.sponsorshipXunta de Galicia; ED431B 2016/013es_ES
dc.description.sponsorshipXunta de Galicia; ED481B 2016/190-0es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.relation.urihttps://doi.org/10.1016/j.fct.2017.02.005es_ES
dc.rightsAtribución-NoComercial-SinDerivadas 4.0 Internacionales_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectA172 cellses_ES
dc.subjectComet assayes_ES
dc.subjectNeurogenotoxicityes_ES
dc.subjectMicronucleus testes_ES
dc.subjectSH-SY5Y cellses_ES
dc.subjectγH2AX assayes_ES
dc.titleComparative Study of Human Neuronal and Glial Cell Sensitivity for in Vitro Neurogenotoxicity Testinges_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
UDC.journalTitleFood and Chemical Toxicologyes_ES
UDC.volume102 (April 2017)es_ES
UDC.startPage120es_ES
UDC.endPage128es_ES
dc.identifier.doi10.1016/j.fct.2017.02.005
UDC.coleccionInvestigaciónes_ES
UDC.departamentoPsicoloxíaes_ES
UDC.grupoInvDiagnóstico Condutual e Molecular Aplicado á Saúde (DICOMOSA)es_ES


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