Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10400.18/2622 |
Resumo: | Microcystins (MC) are cyanotoxins occurring globally, known for causing acute hepatotoxicity in humans/animals, tumor promotion in animals and potential carcinogenicity. The mechanism of MC toxicity is considered a multi-pathway process involving the inhibition of protein phosphatases PP1/PP2A and the production of reactive oxygen species (ROS). However, their mechanism of action is not fully characterized, thus hampering the complete hazard identification. In this study, we evaluated the effect of several microcystin-LR concentrations on the growth, ROS levels, antioxidant system response and apoptosis induction on Saccharomyces cerevisiae. Our results showed that the growth of S. cerevisiae was not inhibited when compared to control cells. However, the staining of cells with DHR123 and DHE revealed an intracellular increase of the ROS levels. This ROS increase resulted in an augment of catalase activity and inhibition of SOD. All these facts suggest that hydrogen peroxide was the main ROS induced by MCLR. Signs of apoptosis were also detected in the cells exposed to toxin. Our results show that S. cerevisiae VL3 displays MCLR toxicity effects known to occur in higher eukaryotes and confirmed that it can be a simple and good model to help further in the elucidation of MCLR molecular mechanisms of toxicity. |
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Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosisMicrocystin-LRSaccharomyces CerevisiaeROSAntioxidant SystemApoptosisGrowthAr e Saúde OcupacionalMicrocystins (MC) are cyanotoxins occurring globally, known for causing acute hepatotoxicity in humans/animals, tumor promotion in animals and potential carcinogenicity. The mechanism of MC toxicity is considered a multi-pathway process involving the inhibition of protein phosphatases PP1/PP2A and the production of reactive oxygen species (ROS). However, their mechanism of action is not fully characterized, thus hampering the complete hazard identification. In this study, we evaluated the effect of several microcystin-LR concentrations on the growth, ROS levels, antioxidant system response and apoptosis induction on Saccharomyces cerevisiae. Our results showed that the growth of S. cerevisiae was not inhibited when compared to control cells. However, the staining of cells with DHR123 and DHE revealed an intracellular increase of the ROS levels. This ROS increase resulted in an augment of catalase activity and inhibition of SOD. All these facts suggest that hydrogen peroxide was the main ROS induced by MCLR. Signs of apoptosis were also detected in the cells exposed to toxin. Our results show that S. cerevisiae VL3 displays MCLR toxicity effects known to occur in higher eukaryotes and confirmed that it can be a simple and good model to help further in the elucidation of MCLR molecular mechanisms of toxicity.This research was partially supported by the European Regional Development Fund (ERDF) through the COMPETE – Operational Competitiveness Programme – and national funds through FCT – Foundation for Science and Technology – under the project PEst-C/MAR/LA0015/2013 and grant (SFRH/BPD/75922/2011) to E. ValérioElsevier/ International Society on ToxinologyRepositório Científico do Instituto Nacional de SaúdeValério, ElisabeteVilares, ArmindaCampos, AlexandrePereira, PauloVasconcelos, Vitor2015-01-09T17:02:50Z2014-112014-11-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/2622engToxicon. 2014 Nov;90:191-8. doi: 10.1016/j.toxicon.2014.08.059. Epub 2014 Aug 230041-010110.1016/j.toxicon.2014.08.059info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-20T15:39:20Zoai:repositorio.insa.pt:10400.18/2622Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:37:32.827848Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
title |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
spellingShingle |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis Valério, Elisabete Microcystin-LR Saccharomyces Cerevisiae ROS Antioxidant System Apoptosis Growth Ar e Saúde Ocupacional |
title_short |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
title_full |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
title_fullStr |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
title_full_unstemmed |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
title_sort |
Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis |
author |
Valério, Elisabete |
author_facet |
Valério, Elisabete Vilares, Arminda Campos, Alexandre Pereira, Paulo Vasconcelos, Vitor |
author_role |
author |
author2 |
Vilares, Arminda Campos, Alexandre Pereira, Paulo Vasconcelos, Vitor |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Repositório Científico do Instituto Nacional de Saúde |
dc.contributor.author.fl_str_mv |
Valério, Elisabete Vilares, Arminda Campos, Alexandre Pereira, Paulo Vasconcelos, Vitor |
dc.subject.por.fl_str_mv |
Microcystin-LR Saccharomyces Cerevisiae ROS Antioxidant System Apoptosis Growth Ar e Saúde Ocupacional |
topic |
Microcystin-LR Saccharomyces Cerevisiae ROS Antioxidant System Apoptosis Growth Ar e Saúde Ocupacional |
description |
Microcystins (MC) are cyanotoxins occurring globally, known for causing acute hepatotoxicity in humans/animals, tumor promotion in animals and potential carcinogenicity. The mechanism of MC toxicity is considered a multi-pathway process involving the inhibition of protein phosphatases PP1/PP2A and the production of reactive oxygen species (ROS). However, their mechanism of action is not fully characterized, thus hampering the complete hazard identification. In this study, we evaluated the effect of several microcystin-LR concentrations on the growth, ROS levels, antioxidant system response and apoptosis induction on Saccharomyces cerevisiae. Our results showed that the growth of S. cerevisiae was not inhibited when compared to control cells. However, the staining of cells with DHR123 and DHE revealed an intracellular increase of the ROS levels. This ROS increase resulted in an augment of catalase activity and inhibition of SOD. All these facts suggest that hydrogen peroxide was the main ROS induced by MCLR. Signs of apoptosis were also detected in the cells exposed to toxin. Our results show that S. cerevisiae VL3 displays MCLR toxicity effects known to occur in higher eukaryotes and confirmed that it can be a simple and good model to help further in the elucidation of MCLR molecular mechanisms of toxicity. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-11 2014-11-01T00:00:00Z 2015-01-09T17:02:50Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.18/2622 |
url |
http://hdl.handle.net/10400.18/2622 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Toxicon. 2014 Nov;90:191-8. doi: 10.1016/j.toxicon.2014.08.059. Epub 2014 Aug 23 0041-0101 10.1016/j.toxicon.2014.08.059 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/embargoedAccess |
eu_rights_str_mv |
embargoedAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier/ International Society on Toxinology |
publisher.none.fl_str_mv |
Elsevier/ International Society on Toxinology |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799132109982400512 |