Effects of microcystin-LR on Saccharomyces cerevisiae growth, oxidative stress and apoptosis

Detalhes bibliográficos
Autor(a) principal: Valério, Elisabete
Data de Publicação: 2014
Outros Autores: Vilares, Arminda, Campos, Alexandre, Pereira, Paulo, Vasconcelos, Vitor
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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spelling 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
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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)
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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
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