Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis

Autores
Gómez Toledo, Alejandro; Golden, Gregory; Rosa Campos, Alexandre; Cuello, Héctor Adrián; Sorrentino, James; Lewis, Nathan; Varki, Nissi; Nizet, Victor; Smith, Jeffrey W.; Esko, Jeffrey D.
Año de publicación
2019
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Sepsis is a life-threatening condition triggered by a dysregulated host response to microbial infection resulting in vascular dysfunction, organ failure and death. Here we provide a semi-quantitative atlas of the murine vascular cell-surface proteome at the organ level, and how it changes during sepsis. Using in vivo chemical labeling and high-resolution mass spectrometry, we demonstrate the presence of a vascular proteome that is perfusable and shared across multiple organs. This proteome is enriched in membrane-anchored proteins, including multiple regulators of endothelial barrier functions and innate immunity. Further, we automated our workflows and applied them to a murine model of methicillin-resistant Staphylococcus aureus (MRSA) sepsis to unravel changes during systemic inflammatory responses. We provide an organ-specific atlas of both systemic and local changes of the vascular proteome triggered by sepsis. Collectively, the data indicates that MRSA-sepsis triggers extensive proteome remodeling of the vascular cell surfaces, in a tissue-specific manner.
Fil: Gómez Toledo, Alejandro. University of California; Estados Unidos
Fil: Golden, Gregory. University of California; Estados Unidos
Fil: Rosa Campos, Alexandre. Sanford-Burnham-Prebys Medical Discovery Institute; Estados Unidos
Fil: Cuello, Héctor Adrián. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Quilmes; Argentina
Fil: Sorrentino, James. University of California at San Diego; Estados Unidos
Fil: Lewis, Nathan. University of California at San Diego; Estados Unidos
Fil: Varki, Nissi. University of California at San Diego; Estados Unidos
Fil: Nizet, Victor. University of California at San Diego; Estados Unidos
Fil: Smith, Jeffrey W.. Sanford-Burnham-Prebys Medical Discovery Institute; Estados Unidos
Fil: Esko, Jeffrey D.. University of California; Estados Unidos
Materia
Proteomics profiling
Sepsis
Vasculopathies
Staphylococcus
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/175720

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network_name_str CONICET Digital (CONICET)
spelling Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsisGómez Toledo, AlejandroGolden, GregoryRosa Campos, AlexandreCuello, Héctor AdriánSorrentino, JamesLewis, NathanVarki, NissiNizet, VictorSmith, Jeffrey W.Esko, Jeffrey D.Proteomics profilingSepsisVasculopathiesStaphylococcushttps://purl.org/becyt/ford/3.3https://purl.org/becyt/ford/3Sepsis is a life-threatening condition triggered by a dysregulated host response to microbial infection resulting in vascular dysfunction, organ failure and death. Here we provide a semi-quantitative atlas of the murine vascular cell-surface proteome at the organ level, and how it changes during sepsis. Using in vivo chemical labeling and high-resolution mass spectrometry, we demonstrate the presence of a vascular proteome that is perfusable and shared across multiple organs. This proteome is enriched in membrane-anchored proteins, including multiple regulators of endothelial barrier functions and innate immunity. Further, we automated our workflows and applied them to a murine model of methicillin-resistant Staphylococcus aureus (MRSA) sepsis to unravel changes during systemic inflammatory responses. We provide an organ-specific atlas of both systemic and local changes of the vascular proteome triggered by sepsis. Collectively, the data indicates that MRSA-sepsis triggers extensive proteome remodeling of the vascular cell surfaces, in a tissue-specific manner.Fil: Gómez Toledo, Alejandro. University of California; Estados UnidosFil: Golden, Gregory. University of California; Estados UnidosFil: Rosa Campos, Alexandre. Sanford-Burnham-Prebys Medical Discovery Institute; Estados UnidosFil: Cuello, Héctor Adrián. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Quilmes; ArgentinaFil: Sorrentino, James. University of California at San Diego; Estados UnidosFil: Lewis, Nathan. University of California at San Diego; Estados UnidosFil: Varki, Nissi. University of California at San Diego; Estados UnidosFil: Nizet, Victor. University of California at San Diego; Estados UnidosFil: Smith, Jeffrey W.. Sanford-Burnham-Prebys Medical Discovery Institute; Estados UnidosFil: Esko, Jeffrey D.. University of California; Estados UnidosNature Publishing Group2019-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/175720Gómez Toledo, Alejandro; Golden, Gregory; Rosa Campos, Alexandre; Cuello, Héctor Adrián; Sorrentino, James; et al.; Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis; Nature Publishing Group; Nature Communications; 10; 1; 12-2019; 1-132041-1723CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-019-12672-xinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:16:20Zoai:ri.conicet.gov.ar:11336/175720instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:16:20.681CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
title Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
spellingShingle Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
Gómez Toledo, Alejandro
Proteomics profiling
Sepsis
Vasculopathies
Staphylococcus
title_short Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
title_full Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
title_fullStr Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
title_full_unstemmed Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
title_sort Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis
dc.creator.none.fl_str_mv Gómez Toledo, Alejandro
Golden, Gregory
Rosa Campos, Alexandre
Cuello, Héctor Adrián
Sorrentino, James
Lewis, Nathan
Varki, Nissi
Nizet, Victor
Smith, Jeffrey W.
Esko, Jeffrey D.
author Gómez Toledo, Alejandro
author_facet Gómez Toledo, Alejandro
Golden, Gregory
Rosa Campos, Alexandre
Cuello, Héctor Adrián
Sorrentino, James
Lewis, Nathan
Varki, Nissi
Nizet, Victor
Smith, Jeffrey W.
Esko, Jeffrey D.
author_role author
author2 Golden, Gregory
Rosa Campos, Alexandre
Cuello, Héctor Adrián
Sorrentino, James
Lewis, Nathan
Varki, Nissi
Nizet, Victor
Smith, Jeffrey W.
Esko, Jeffrey D.
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Proteomics profiling
Sepsis
Vasculopathies
Staphylococcus
topic Proteomics profiling
Sepsis
Vasculopathies
Staphylococcus
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.3
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Sepsis is a life-threatening condition triggered by a dysregulated host response to microbial infection resulting in vascular dysfunction, organ failure and death. Here we provide a semi-quantitative atlas of the murine vascular cell-surface proteome at the organ level, and how it changes during sepsis. Using in vivo chemical labeling and high-resolution mass spectrometry, we demonstrate the presence of a vascular proteome that is perfusable and shared across multiple organs. This proteome is enriched in membrane-anchored proteins, including multiple regulators of endothelial barrier functions and innate immunity. Further, we automated our workflows and applied them to a murine model of methicillin-resistant Staphylococcus aureus (MRSA) sepsis to unravel changes during systemic inflammatory responses. We provide an organ-specific atlas of both systemic and local changes of the vascular proteome triggered by sepsis. Collectively, the data indicates that MRSA-sepsis triggers extensive proteome remodeling of the vascular cell surfaces, in a tissue-specific manner.
Fil: Gómez Toledo, Alejandro. University of California; Estados Unidos
Fil: Golden, Gregory. University of California; Estados Unidos
Fil: Rosa Campos, Alexandre. Sanford-Burnham-Prebys Medical Discovery Institute; Estados Unidos
Fil: Cuello, Héctor Adrián. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Quilmes; Argentina
Fil: Sorrentino, James. University of California at San Diego; Estados Unidos
Fil: Lewis, Nathan. University of California at San Diego; Estados Unidos
Fil: Varki, Nissi. University of California at San Diego; Estados Unidos
Fil: Nizet, Victor. University of California at San Diego; Estados Unidos
Fil: Smith, Jeffrey W.. Sanford-Burnham-Prebys Medical Discovery Institute; Estados Unidos
Fil: Esko, Jeffrey D.. University of California; Estados Unidos
description Sepsis is a life-threatening condition triggered by a dysregulated host response to microbial infection resulting in vascular dysfunction, organ failure and death. Here we provide a semi-quantitative atlas of the murine vascular cell-surface proteome at the organ level, and how it changes during sepsis. Using in vivo chemical labeling and high-resolution mass spectrometry, we demonstrate the presence of a vascular proteome that is perfusable and shared across multiple organs. This proteome is enriched in membrane-anchored proteins, including multiple regulators of endothelial barrier functions and innate immunity. Further, we automated our workflows and applied them to a murine model of methicillin-resistant Staphylococcus aureus (MRSA) sepsis to unravel changes during systemic inflammatory responses. We provide an organ-specific atlas of both systemic and local changes of the vascular proteome triggered by sepsis. Collectively, the data indicates that MRSA-sepsis triggers extensive proteome remodeling of the vascular cell surfaces, in a tissue-specific manner.
publishDate 2019
dc.date.none.fl_str_mv 2019-12
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/175720
Gómez Toledo, Alejandro; Golden, Gregory; Rosa Campos, Alexandre; Cuello, Héctor Adrián; Sorrentino, James; et al.; Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis; Nature Publishing Group; Nature Communications; 10; 1; 12-2019; 1-13
2041-1723
CONICET Digital
CONICET
url http://hdl.handle.net/11336/175720
identifier_str_mv Gómez Toledo, Alejandro; Golden, Gregory; Rosa Campos, Alexandre; Cuello, Héctor Adrián; Sorrentino, James; et al.; Proteomic atlas of organ vasculopathies triggered by Staphylococcus aureus sepsis; Nature Publishing Group; Nature Communications; 10; 1; 12-2019; 1-13
2041-1723
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-019-12672-x
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Nature Publishing Group
publisher.none.fl_str_mv Nature Publishing Group
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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