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dc.contributor.authorValdiglesias, Vanessa
dc.contributor.authorLaffon, Blanca
dc.contributor.authorPásaro, Eduardo
dc.contributor.authorMéndez, Josefina
dc.date.accessioned2024-01-10T16:41:45Z
dc.date.available2024-01-10T16:41:45Z
dc.date.issued2011-03-28
dc.identifier.citationV. Valdiglesias, B. Laffon, E. Pásaro and J. Méndez, Okadaic acid induces morphological changes, apoptosis and cell cycle alterations in different human cell types, J. Environ. Monit., 2011,13, 1831-1840, https://doi.org/10.1039/C0EM00771Des_ES
dc.identifier.issn1464-0333
dc.identifier.urihttp://hdl.handle.net/2183/34802
dc.descriptionThis version of the article has been accepted for publication, after peer review, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: https://doi.org/10.1039/C0EM00771Des_ES
dc.description.abstract[Abstract] Okadaic acid (OA) is a marine toxin produced by dinoflagellate species which is frequently accumulated in molluscs usual in the human diet. The exact action mechanism of OA has not been described yet and the results of most reported studies are often conflicting. The aim of this work was to evaluate the OA effects on morphology, cell cycle and apoptosis induction by means of light microscopy and flow cytometry, in three different types of human cells (leukocytes, HepG2 cells and SHSY5Y cells). Cells were treated with a range of OA concentrations in the presence and absence of S9 fraction. OA induced morphological changes in all the cell types studied, and cell cycle disruption only in leukocytes and neuronal cells. SHSY5Y cells were the most sensitive to OA assault. Results obtained in the presence and absence of metabolic activation were similar, suggesting that OA acts both directly and indirectly. Furthermore, OA was found to increase the subG1 region in the flow cytometry cell cycle analysis, suggesting induction of apoptosis. These results were confirmed by the employment of specific methodologies for studying apoptosis such as caspase 3 activation and annexin V staining. Increases in the apoptosis rate were obtained in all the cells treated in the absence of S9 fraction, accompanied by increases in caspase 3 activation, suggesting that apoptosis induced by OA is a caspase 3-dependent process. Nevertheless, in the presence of S9 fraction no apoptosis was detected, indicating a metabolic detoxifying activity, although necrosis was observed in neuroblastoma cells.es_ES
dc.description.sponsorshipThis work was funded by a grant from the Xunta de Galicia (INCITE08PXIB106155PR). V. Valdiglesias was supported by a fellowship from the University of A Coruñaes_ES
dc.description.sponsorshipGalicia.Xunta; INCITE08PXIB106155PRes_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (Gran Bretaña)es_ES
dc.relation.urihttps://doi.org/10.1039/C0EM00771Des_ES
dc.titleOkadaic Acid Induces Morphological Changes, Apoptosis and Cell Cycle Alterations in Different Human Cell Typeses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleJournal of Environmental Monitoringes_ES
UDC.volume13 (2011)es_ES
UDC.issue6es_ES
UDC.startPage1831es_ES
UDC.endPage1840es_ES
dc.identifier.doi10.1039/C0EM00771D


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