Activity and Cell-Death Pathway in Leishmania infantum Induced by Sugiol: Vectorization Using Yeast Cell Wall Particles Obtained From Saccharomyces cerevisiae
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , |
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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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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7160 |
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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 |
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 |
|
_version_ |
1822218240464519168 |
dc.identifier.doi.none.fl_str_mv |
10.3389/fcimb.2019.00208 |