Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity

Detalhes bibliográficos
Autor(a) principal: Tagliari, Loriane [UNIFESP]
Data de Publicação: 2012
Outros Autores: Toledo, Marcos Sergio de [UNIFESP], Lacerda, Tanil G [UNIFESP], Suzuki, Erika [UNIFESP], Straus, Anita Hilda [UNIFESP], Takahashi, Helio Kiyoshi [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.bbamem.2011.12.008
http://repositorio.unifesp.br/handle/11600/34631
Resumo: Analysis of membrane lipids of Histoplasma capsulatum showed that similar to 40% of fungal ergosterol is present in membrane microdomain fractions resistant to treatment with non-ionic detergent at 4 degrees C. Specific proteins were also enriched in these fractions, particularly Pma1p a yeast microdomain protein marker (a plasma membrane proton ATPase), a 30 kDa laminin-binding protein, and a 50 kDa protein recognized by anti-alpha 5-integrin antibody. To better understand the role of ergosterol-dependent microdomains in fungal biology and pathogenicity, H. capsulatum yeast forms were treated with a sterol chelator, methyl-beta-cyclodextrin (m beta CD). Removal of ergosterol by m beta CD incubation led to disorganization of ergosterol-enriched microdomains containing Pma1p and the 30 kDa protein, resulting in displacement of these proteins from detergent-insoluble to -soluble fractions in sucrose density gradient ultracentrifugation. m beta CD treatment did not displace/remove the 50 kDa alpha 5-integrin-like protein nor had effect on the organization of glycosphingolipids present in the detergent-resistant fractions. Ergosterol-enriched membrane microdomains were also shown to be important for infectivity of alveolar macrophages; after treatment of yeasts with m beta CD, macrophage infectivity was reduced by 45%. These findings suggest the existence of two populations of detergent-resistant membrane microdomains in H. capsulatum yeast forms: (i) ergosterol-independent microdomains rich in integrin-like proteins and glycosphingolipids, possibly involved in signal transduction; (ii) ergosterol-enriched microdomains containing Pma1p and the 30 kDa laminin-binding protein; ergosterol and/or the 30 kDa protein may be involved in macrophage infectivity. (C) 2011 Elsevier B.V. All rights reserved.
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spelling Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivityHistoplasma capsulatumMembrane microdomainErgosterolMacrophage infectivityGlycosphingolipidsMethyl-beta-cyclodextrinAnalysis of membrane lipids of Histoplasma capsulatum showed that similar to 40% of fungal ergosterol is present in membrane microdomain fractions resistant to treatment with non-ionic detergent at 4 degrees C. Specific proteins were also enriched in these fractions, particularly Pma1p a yeast microdomain protein marker (a plasma membrane proton ATPase), a 30 kDa laminin-binding protein, and a 50 kDa protein recognized by anti-alpha 5-integrin antibody. To better understand the role of ergosterol-dependent microdomains in fungal biology and pathogenicity, H. capsulatum yeast forms were treated with a sterol chelator, methyl-beta-cyclodextrin (m beta CD). Removal of ergosterol by m beta CD incubation led to disorganization of ergosterol-enriched microdomains containing Pma1p and the 30 kDa protein, resulting in displacement of these proteins from detergent-insoluble to -soluble fractions in sucrose density gradient ultracentrifugation. m beta CD treatment did not displace/remove the 50 kDa alpha 5-integrin-like protein nor had effect on the organization of glycosphingolipids present in the detergent-resistant fractions. Ergosterol-enriched membrane microdomains were also shown to be important for infectivity of alveolar macrophages; after treatment of yeasts with m beta CD, macrophage infectivity was reduced by 45%. These findings suggest the existence of two populations of detergent-resistant membrane microdomains in H. capsulatum yeast forms: (i) ergosterol-independent microdomains rich in integrin-like proteins and glycosphingolipids, possibly involved in signal transduction; (ii) ergosterol-enriched microdomains containing Pma1p and the 30 kDa laminin-binding protein; ergosterol and/or the 30 kDa protein may be involved in macrophage infectivity. (C) 2011 Elsevier B.V. All rights reserved.Universidade Federal de São Paulo, Div Glycoconjugate Immunochem, Dept Biochem, Escola Paulista Med, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Immunol & Parasitol, Escola Paulista Med, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Div Glycoconjugate Immunochem, Dept Biochem, Escola Paulista Med, BR-04023900 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Immunol & Parasitol, Escola Paulista Med, BR-04023900 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Elsevier B.V.Universidade Federal de São Paulo (UNIFESP)Tagliari, Loriane [UNIFESP]Toledo, Marcos Sergio de [UNIFESP]Lacerda, Tanil G [UNIFESP]Suzuki, Erika [UNIFESP]Straus, Anita Hilda [UNIFESP]Takahashi, Helio Kiyoshi [UNIFESP]2016-01-24T14:17:55Z2016-01-24T14:17:55Z2012-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion458-466application/pdfhttp://dx.doi.org/10.1016/j.bbamem.2011.12.008Biochimica Et Biophysica Acta-biomembranes. Amsterdam: Elsevier B.V., v. 1818, n. 3, p. 458-466, 2012.10.1016/j.bbamem.2011.12.008WOS000301155600012.pdf0005-2736http://repositorio.unifesp.br/handle/11600/34631WOS:000301155600012engBiochimica Et Biophysica Acta-biomembranesinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-01T00:16:22Zoai:repositorio.unifesp.br/:11600/34631Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-01T00:16:22Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
title Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
spellingShingle Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
Tagliari, Loriane [UNIFESP]
Histoplasma capsulatum
Membrane microdomain
Ergosterol
Macrophage infectivity
Glycosphingolipids
Methyl-beta-cyclodextrin
title_short Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
title_full Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
title_fullStr Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
title_full_unstemmed Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
title_sort Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
author Tagliari, Loriane [UNIFESP]
author_facet Tagliari, Loriane [UNIFESP]
Toledo, Marcos Sergio de [UNIFESP]
Lacerda, Tanil G [UNIFESP]
Suzuki, Erika [UNIFESP]
Straus, Anita Hilda [UNIFESP]
Takahashi, Helio Kiyoshi [UNIFESP]
author_role author
author2 Toledo, Marcos Sergio de [UNIFESP]
Lacerda, Tanil G [UNIFESP]
Suzuki, Erika [UNIFESP]
Straus, Anita Hilda [UNIFESP]
Takahashi, Helio Kiyoshi [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Tagliari, Loriane [UNIFESP]
Toledo, Marcos Sergio de [UNIFESP]
Lacerda, Tanil G [UNIFESP]
Suzuki, Erika [UNIFESP]
Straus, Anita Hilda [UNIFESP]
Takahashi, Helio Kiyoshi [UNIFESP]
dc.subject.por.fl_str_mv Histoplasma capsulatum
Membrane microdomain
Ergosterol
Macrophage infectivity
Glycosphingolipids
Methyl-beta-cyclodextrin
topic Histoplasma capsulatum
Membrane microdomain
Ergosterol
Macrophage infectivity
Glycosphingolipids
Methyl-beta-cyclodextrin
description Analysis of membrane lipids of Histoplasma capsulatum showed that similar to 40% of fungal ergosterol is present in membrane microdomain fractions resistant to treatment with non-ionic detergent at 4 degrees C. Specific proteins were also enriched in these fractions, particularly Pma1p a yeast microdomain protein marker (a plasma membrane proton ATPase), a 30 kDa laminin-binding protein, and a 50 kDa protein recognized by anti-alpha 5-integrin antibody. To better understand the role of ergosterol-dependent microdomains in fungal biology and pathogenicity, H. capsulatum yeast forms were treated with a sterol chelator, methyl-beta-cyclodextrin (m beta CD). Removal of ergosterol by m beta CD incubation led to disorganization of ergosterol-enriched microdomains containing Pma1p and the 30 kDa protein, resulting in displacement of these proteins from detergent-insoluble to -soluble fractions in sucrose density gradient ultracentrifugation. m beta CD treatment did not displace/remove the 50 kDa alpha 5-integrin-like protein nor had effect on the organization of glycosphingolipids present in the detergent-resistant fractions. Ergosterol-enriched membrane microdomains were also shown to be important for infectivity of alveolar macrophages; after treatment of yeasts with m beta CD, macrophage infectivity was reduced by 45%. These findings suggest the existence of two populations of detergent-resistant membrane microdomains in H. capsulatum yeast forms: (i) ergosterol-independent microdomains rich in integrin-like proteins and glycosphingolipids, possibly involved in signal transduction; (ii) ergosterol-enriched microdomains containing Pma1p and the 30 kDa laminin-binding protein; ergosterol and/or the 30 kDa protein may be involved in macrophage infectivity. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2012
dc.date.none.fl_str_mv 2012-03-01
2016-01-24T14:17:55Z
2016-01-24T14:17:55Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.bbamem.2011.12.008
Biochimica Et Biophysica Acta-biomembranes. Amsterdam: Elsevier B.V., v. 1818, n. 3, p. 458-466, 2012.
10.1016/j.bbamem.2011.12.008
WOS000301155600012.pdf
0005-2736
http://repositorio.unifesp.br/handle/11600/34631
WOS:000301155600012
url http://dx.doi.org/10.1016/j.bbamem.2011.12.008
http://repositorio.unifesp.br/handle/11600/34631
identifier_str_mv Biochimica Et Biophysica Acta-biomembranes. Amsterdam: Elsevier B.V., v. 1818, n. 3, p. 458-466, 2012.
10.1016/j.bbamem.2011.12.008
WOS000301155600012.pdf
0005-2736
WOS:000301155600012
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biochimica Et Biophysica Acta-biomembranes
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.format.none.fl_str_mv 458-466
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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