Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae

Detalhes bibliográficos
Autor(a) principal: Scariot, Débora Botura
Data de Publicação: 2019
Outros Autores: Volpato, Hélito, Fernandes, Nilma de Souza, Soares, Edna Filipa Pais, Ueda-Nakamura, Tânia, Dias-Filho, Benedito Prado, Din, Zia Ud, Rodrigues-Filho, Edson, Rubira, Adley Forti, Borges, Olga, Sousa, Maria Céu, Nakamura, Celso Vataru
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
DOI: 10.3389/fcimb.2019.00208
Texto Completo: http://hdl.handle.net/10316/106950
https://doi.org/10.3389/fcimb.2019.00208
Resumo: Visceral leishmaniasis, caused by Leishmania infantum, is a neglected tropical disease, to which efforts in the innovation of effective and affordable treatments remain limited, despite the rising incidence in several regions of the world. In this work, the antileishmanial effects of sugiol were investigated in vitro. This compound was isolated from the bark of Cupressus lusitanica and showed promising activity against L. infantum. In spite of the positive results, it is known that the compound is a poorly water-soluble diterpene molecule, which hinders further investigation, especially in preclinical animal studies. Thus, in an alternative delivery method, sugiol was entrapped in glucan-rich particles obtained from Saccharomyces cerevisiae yeast cell walls (YCWPs). To evaluate the activity of sugiol, the experiments were divided into two parts: (i) the in vitro investigation of antileishmanial activity of free sugiol against L. infantum promastigotes after 24, 48, and 72 h of treatment and (ii) the evaluation of antileishmanial activity of sugiol entrapped in glucan-rich particles against intracellular L. infantum amastigotes. Free sugiol induced the cell-death process in promastigotes, which was triggered by enhancing cytosolic calcium level and promoting the autophagy up to the first 24 h. Over time, the presence of autophagic vacuoles became rarer, especially after treatment with lower concentrations of sugiol, but other cellular events intensified, like ROS production, cell shrinkage, and phosphatidylserine exposure. Hyperpolarization of mitochondrial membrane potential was found at 72 h, induced by the mitochondria calcium uptake, causing an increase in ROS production and lipid peroxidation as a consequence. These events resulted in the cell death of promastigotes by secondary necrosis. Sugiol entrapped in glucan-rich particles was specifically recognized by dectin-1 receptor on the plasma membrane of macrophages, the main host cell of Leishmania spp. Electron micrographs revealed particles containing sugiol within the infected macrophages and these particles were active against the intracellular L. infantum amastigotes without affecting the host cell. Therefore, the YCWPs act like a Trojan horse to successfully deliver sugiol into the macrophage, presenting an interesting strategy to deliver water-insoluble drugs to parasitized cells.
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spelling Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiaeyeast cell wall particlesugiolglucanmacrophageantileishmanial activityAnimalsAntiprotozoal AgentsAutophagyCalciumCell DeathCell WallDisease Models, AnimalDiterpenesFemaleGlucansLectins, C-TypeLeishmania infantumLeishmaniasis, VisceralMacrophagesMembrane Potential, MitochondrialMice, Inbred BALB CMitochondriaMitochondrial MembranesReactive Oxygen SpeciesSaccharomyces cerevisiaeVisceral leishmaniasis, caused by Leishmania infantum, is a neglected tropical disease, to which efforts in the innovation of effective and affordable treatments remain limited, despite the rising incidence in several regions of the world. In this work, the antileishmanial effects of sugiol were investigated in vitro. This compound was isolated from the bark of Cupressus lusitanica and showed promising activity against L. infantum. In spite of the positive results, it is known that the compound is a poorly water-soluble diterpene molecule, which hinders further investigation, especially in preclinical animal studies. Thus, in an alternative delivery method, sugiol was entrapped in glucan-rich particles obtained from Saccharomyces cerevisiae yeast cell walls (YCWPs). To evaluate the activity of sugiol, the experiments were divided into two parts: (i) the in vitro investigation of antileishmanial activity of free sugiol against L. infantum promastigotes after 24, 48, and 72 h of treatment and (ii) the evaluation of antileishmanial activity of sugiol entrapped in glucan-rich particles against intracellular L. infantum amastigotes. Free sugiol induced the cell-death process in promastigotes, which was triggered by enhancing cytosolic calcium level and promoting the autophagy up to the first 24 h. Over time, the presence of autophagic vacuoles became rarer, especially after treatment with lower concentrations of sugiol, but other cellular events intensified, like ROS production, cell shrinkage, and phosphatidylserine exposure. Hyperpolarization of mitochondrial membrane potential was found at 72 h, induced by the mitochondria calcium uptake, causing an increase in ROS production and lipid peroxidation as a consequence. These events resulted in the cell death of promastigotes by secondary necrosis. Sugiol entrapped in glucan-rich particles was specifically recognized by dectin-1 receptor on the plasma membrane of macrophages, the main host cell of Leishmania spp. Electron micrographs revealed particles containing sugiol within the infected macrophages and these particles were active against the intracellular L. infantum amastigotes without affecting the host cell. Therefore, the YCWPs act like a Trojan horse to successfully deliver sugiol into the macrophage, presenting an interesting strategy to deliver water-insoluble drugs to parasitized cells.Frontiers Media S.A.2019info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/106950http://hdl.handle.net/10316/106950https://doi.org/10.3389/fcimb.2019.00208eng2235-2988Scariot, Débora BoturaVolpato, HélitoFernandes, Nilma de SouzaSoares, Edna Filipa PaisUeda-Nakamura, TâniaDias-Filho, Benedito PradoDin, Zia UdRodrigues-Filho, EdsonRubira, Adley FortiBorges, OlgaSousa, Maria CéuNakamura, Celso Vataruinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-05-04T08:32:48Zoai:estudogeral.uc.pt:10316/106950Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:23:20.414486Repositório 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 Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
title Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
spellingShingle Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
Scariot, Débora Botura
yeast cell wall particle
sugiol
glucan
macrophage
antileishmanial activity
Animals
Antiprotozoal Agents
Autophagy
Calcium
Cell Death
Cell Wall
Disease Models, Animal
Diterpenes
Female
Glucans
Lectins, C-Type
Leishmania infantum
Leishmaniasis, Visceral
Macrophages
Membrane Potential, Mitochondrial
Mice, Inbred BALB C
Mitochondria
Mitochondrial Membranes
Reactive Oxygen Species
Saccharomyces cerevisiae
Scariot, Débora Botura
yeast cell wall particle
sugiol
glucan
macrophage
antileishmanial activity
Animals
Antiprotozoal Agents
Autophagy
Calcium
Cell Death
Cell Wall
Disease Models, Animal
Diterpenes
Female
Glucans
Lectins, C-Type
Leishmania infantum
Leishmaniasis, Visceral
Macrophages
Membrane Potential, Mitochondrial
Mice, Inbred BALB C
Mitochondria
Mitochondrial Membranes
Reactive Oxygen Species
Saccharomyces cerevisiae
title_short Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
title_full Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
title_fullStr Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
title_full_unstemmed Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
title_sort Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
author Scariot, Débora Botura
author_facet Scariot, Débora Botura
Scariot, Débora Botura
Volpato, Hélito
Fernandes, Nilma de Souza
Soares, Edna Filipa Pais
Ueda-Nakamura, Tânia
Dias-Filho, Benedito Prado
Din, Zia Ud
Rodrigues-Filho, Edson
Rubira, Adley Forti
Borges, Olga
Sousa, Maria Céu
Nakamura, Celso Vataru
Volpato, Hélito
Fernandes, Nilma de Souza
Soares, Edna Filipa Pais
Ueda-Nakamura, Tânia
Dias-Filho, Benedito Prado
Din, Zia Ud
Rodrigues-Filho, Edson
Rubira, Adley Forti
Borges, Olga
Sousa, Maria Céu
Nakamura, Celso Vataru
author_role author
author2 Volpato, Hélito
Fernandes, Nilma de Souza
Soares, Edna Filipa Pais
Ueda-Nakamura, Tânia
Dias-Filho, Benedito Prado
Din, Zia Ud
Rodrigues-Filho, Edson
Rubira, Adley Forti
Borges, Olga
Sousa, Maria Céu
Nakamura, Celso Vataru
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Scariot, Débora Botura
Volpato, Hélito
Fernandes, Nilma de Souza
Soares, Edna Filipa Pais
Ueda-Nakamura, Tânia
Dias-Filho, Benedito Prado
Din, Zia Ud
Rodrigues-Filho, Edson
Rubira, Adley Forti
Borges, Olga
Sousa, Maria Céu
Nakamura, Celso Vataru
dc.subject.por.fl_str_mv yeast cell wall particle
sugiol
glucan
macrophage
antileishmanial activity
Animals
Antiprotozoal Agents
Autophagy
Calcium
Cell Death
Cell Wall
Disease Models, Animal
Diterpenes
Female
Glucans
Lectins, C-Type
Leishmania infantum
Leishmaniasis, Visceral
Macrophages
Membrane Potential, Mitochondrial
Mice, Inbred BALB C
Mitochondria
Mitochondrial Membranes
Reactive Oxygen Species
Saccharomyces cerevisiae
topic yeast cell wall particle
sugiol
glucan
macrophage
antileishmanial activity
Animals
Antiprotozoal Agents
Autophagy
Calcium
Cell Death
Cell Wall
Disease Models, Animal
Diterpenes
Female
Glucans
Lectins, C-Type
Leishmania infantum
Leishmaniasis, Visceral
Macrophages
Membrane Potential, Mitochondrial
Mice, Inbred BALB C
Mitochondria
Mitochondrial Membranes
Reactive Oxygen Species
Saccharomyces cerevisiae
description Visceral leishmaniasis, caused by Leishmania infantum, is a neglected tropical disease, to which efforts in the innovation of effective and affordable treatments remain limited, despite the rising incidence in several regions of the world. In this work, the antileishmanial effects of sugiol were investigated in vitro. This compound was isolated from the bark of Cupressus lusitanica and showed promising activity against L. infantum. In spite of the positive results, it is known that the compound is a poorly water-soluble diterpene molecule, which hinders further investigation, especially in preclinical animal studies. Thus, in an alternative delivery method, sugiol was entrapped in glucan-rich particles obtained from Saccharomyces cerevisiae yeast cell walls (YCWPs). To evaluate the activity of sugiol, the experiments were divided into two parts: (i) the in vitro investigation of antileishmanial activity of free sugiol against L. infantum promastigotes after 24, 48, and 72 h of treatment and (ii) the evaluation of antileishmanial activity of sugiol entrapped in glucan-rich particles against intracellular L. infantum amastigotes. Free sugiol induced the cell-death process in promastigotes, which was triggered by enhancing cytosolic calcium level and promoting the autophagy up to the first 24 h. Over time, the presence of autophagic vacuoles became rarer, especially after treatment with lower concentrations of sugiol, but other cellular events intensified, like ROS production, cell shrinkage, and phosphatidylserine exposure. Hyperpolarization of mitochondrial membrane potential was found at 72 h, induced by the mitochondria calcium uptake, causing an increase in ROS production and lipid peroxidation as a consequence. These events resulted in the cell death of promastigotes by secondary necrosis. Sugiol entrapped in glucan-rich particles was specifically recognized by dectin-1 receptor on the plasma membrane of macrophages, the main host cell of Leishmania spp. Electron micrographs revealed particles containing sugiol within the infected macrophages and these particles were active against the intracellular L. infantum amastigotes without affecting the host cell. Therefore, the YCWPs act like a Trojan horse to successfully deliver sugiol into the macrophage, presenting an interesting strategy to deliver water-insoluble drugs to parasitized cells.
publishDate 2019
dc.date.none.fl_str_mv 2019
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/10316/106950
http://hdl.handle.net/10316/106950
https://doi.org/10.3389/fcimb.2019.00208
url http://hdl.handle.net/10316/106950
https://doi.org/10.3389/fcimb.2019.00208
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2235-2988
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Frontiers Media S.A.
publisher.none.fl_str_mv Frontiers Media S.A.
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
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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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dc.identifier.doi.none.fl_str_mv 10.3389/fcimb.2019.00208