Membrane microdomain components of Histoplasma capsulatum yeast forms, and their role in alveolar macrophage infectivity
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1814268357800624128 |