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
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- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/175720
Ver los metadatos del registro completo
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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 Técnicas2025-11-05T10:21:15Zoai: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:34982025-11-05 10:21:16.116CONICET 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 |
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article |
| status_str |
publishedVersion |
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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 |
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eng |
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eng |
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Nature Publishing Group |
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Nature Publishing Group |
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