Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.3390/toxins11080443 http://hdl.handle.net/11449/189495 |
Resumo: | Gliotoxin (GTX) is the major and the most potent mycotoxin that is secreted by Aspergillus fumigatus, which is capable of injuring and killing microglial cells, astrocytes, and oligodendrocytes. During the last years, studies with patients and experimental models of multiple sclerosis (MS), which is an autoimmune disease of the central nervous system (CNS), suggested that fungal infections are among the possible initiators or aggravators of this pathology. The deleterious effect can occur through a direct interaction of the fungus with the CNS or by the toxin release from a non-neurological site. In the present work, we investigated the effect of GTX on experimental autoimmune encephalomyelitis (EAE) development. Female C57BL/6 mice were immunized with myelin oligodendrocyte glycoprotein and then intraperitoneally injected with three doses of GTX (1 mg/kg b.w., each) on days 4, 7, and 10. GTX aggravated clinical symptoms of the disease in a dose-dependent way and this outcome was concomitant with an increased neuroinflammation. CNS analyses revealed that GTX locally increased the relative expression of inflammatory genes and the cytokine production. Our results indicate that GTX administered in a non-neuronal site was able to increase neuroinflammation in EAE. Other mycotoxins could also be deleterious to many neurological diseases by similar mechanisms. |
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Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammationExperimental autoimmune encephalomyelitisGliotoxinImmunomodulationMultiple sclerosisMycotoxinGliotoxin (GTX) is the major and the most potent mycotoxin that is secreted by Aspergillus fumigatus, which is capable of injuring and killing microglial cells, astrocytes, and oligodendrocytes. During the last years, studies with patients and experimental models of multiple sclerosis (MS), which is an autoimmune disease of the central nervous system (CNS), suggested that fungal infections are among the possible initiators or aggravators of this pathology. The deleterious effect can occur through a direct interaction of the fungus with the CNS or by the toxin release from a non-neurological site. In the present work, we investigated the effect of GTX on experimental autoimmune encephalomyelitis (EAE) development. Female C57BL/6 mice were immunized with myelin oligodendrocyte glycoprotein and then intraperitoneally injected with three doses of GTX (1 mg/kg b.w., each) on days 4, 7, and 10. GTX aggravated clinical symptoms of the disease in a dose-dependent way and this outcome was concomitant with an increased neuroinflammation. CNS analyses revealed that GTX locally increased the relative expression of inflammatory genes and the cytokine production. Our results indicate that GTX administered in a non-neuronal site was able to increase neuroinflammation in EAE. Other mycotoxins could also be deleterious to many neurological diseases by similar mechanisms.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Department of Microbiology and Immunology Institute of Biosciences of Botucatu São Paulo State University (UNESP)Department of Biological Sciences School of Sciences São Paulo State University (UNESP)Department of Tropical Diseases and Image Diagnosis Botucatu Medical School São Paulo State University (UNESP)Department of Microbiology and Immunology Institute of Biosciences of Botucatu São Paulo State University (UNESP)Department of Biological Sciences School of Sciences São Paulo State University (UNESP)Department of Tropical Diseases and Image Diagnosis Botucatu Medical School São Paulo State University (UNESP)FAPESP: #2013/14353-2FAPESP: 2012/12540-7FAPESP: 2013/14353-2Universidade Estadual Paulista (Unesp)Fraga-Silva, Thais Fernanda de Campos [UNESP]Mimura, Luiza Ayumi Nishiyama [UNESP]Leite, Laysla de Campos Toledo [UNESP]Borim, Patrícia Aparecida [UNESP]Ishikawa, Larissa Lumi Watanabe [UNESP]Venturini, James [UNESP]de Arruda, Maria Sueli Parreira [UNESP]Sartori, Alexandrina [UNESP]2019-10-06T16:42:34Z2019-10-06T16:42:34Z2019-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.3390/toxins11080443Toxins, v. 11, n. 8, 2019.2072-6651http://hdl.handle.net/11449/18949510.3390/toxins110804432-s2.0-85070321144Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengToxinsinfo:eu-repo/semantics/openAccess2024-08-15T15:23:00Zoai:repositorio.unesp.br:11449/189495Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-15T15:23Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
title |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
spellingShingle |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation Fraga-Silva, Thais Fernanda de Campos [UNESP] Experimental autoimmune encephalomyelitis Gliotoxin Immunomodulation Multiple sclerosis Mycotoxin |
title_short |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
title_full |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
title_fullStr |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
title_full_unstemmed |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
title_sort |
Gliotoxin aggravates experimental autoimmune encephalomyelitis by triggering neuroinflammation |
author |
Fraga-Silva, Thais Fernanda de Campos [UNESP] |
author_facet |
Fraga-Silva, Thais Fernanda de Campos [UNESP] Mimura, Luiza Ayumi Nishiyama [UNESP] Leite, Laysla de Campos Toledo [UNESP] Borim, Patrícia Aparecida [UNESP] Ishikawa, Larissa Lumi Watanabe [UNESP] Venturini, James [UNESP] de Arruda, Maria Sueli Parreira [UNESP] Sartori, Alexandrina [UNESP] |
author_role |
author |
author2 |
Mimura, Luiza Ayumi Nishiyama [UNESP] Leite, Laysla de Campos Toledo [UNESP] Borim, Patrícia Aparecida [UNESP] Ishikawa, Larissa Lumi Watanabe [UNESP] Venturini, James [UNESP] de Arruda, Maria Sueli Parreira [UNESP] Sartori, Alexandrina [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Fraga-Silva, Thais Fernanda de Campos [UNESP] Mimura, Luiza Ayumi Nishiyama [UNESP] Leite, Laysla de Campos Toledo [UNESP] Borim, Patrícia Aparecida [UNESP] Ishikawa, Larissa Lumi Watanabe [UNESP] Venturini, James [UNESP] de Arruda, Maria Sueli Parreira [UNESP] Sartori, Alexandrina [UNESP] |
dc.subject.por.fl_str_mv |
Experimental autoimmune encephalomyelitis Gliotoxin Immunomodulation Multiple sclerosis Mycotoxin |
topic |
Experimental autoimmune encephalomyelitis Gliotoxin Immunomodulation Multiple sclerosis Mycotoxin |
description |
Gliotoxin (GTX) is the major and the most potent mycotoxin that is secreted by Aspergillus fumigatus, which is capable of injuring and killing microglial cells, astrocytes, and oligodendrocytes. During the last years, studies with patients and experimental models of multiple sclerosis (MS), which is an autoimmune disease of the central nervous system (CNS), suggested that fungal infections are among the possible initiators or aggravators of this pathology. The deleterious effect can occur through a direct interaction of the fungus with the CNS or by the toxin release from a non-neurological site. In the present work, we investigated the effect of GTX on experimental autoimmune encephalomyelitis (EAE) development. Female C57BL/6 mice were immunized with myelin oligodendrocyte glycoprotein and then intraperitoneally injected with three doses of GTX (1 mg/kg b.w., each) on days 4, 7, and 10. GTX aggravated clinical symptoms of the disease in a dose-dependent way and this outcome was concomitant with an increased neuroinflammation. CNS analyses revealed that GTX locally increased the relative expression of inflammatory genes and the cytokine production. Our results indicate that GTX administered in a non-neuronal site was able to increase neuroinflammation in EAE. Other mycotoxins could also be deleterious to many neurological diseases by similar mechanisms. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-06T16:42:34Z 2019-10-06T16:42:34Z 2019-08-01 |
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://dx.doi.org/10.3390/toxins11080443 Toxins, v. 11, n. 8, 2019. 2072-6651 http://hdl.handle.net/11449/189495 10.3390/toxins11080443 2-s2.0-85070321144 |
url |
http://dx.doi.org/10.3390/toxins11080443 http://hdl.handle.net/11449/189495 |
identifier_str_mv |
Toxins, v. 11, n. 8, 2019. 2072-6651 10.3390/toxins11080443 2-s2.0-85070321144 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Toxins |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
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1808128159964463104 |