Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent
- Autores
- Díaz Ludovico, Ivo; Trejo, Sebastian Alejandro; Becerra, Romina Valeria; Garda, Horacio Alberto; Gonzalez, Marina Cecilia
- Año de publicación
- 2020
- Idioma
- inglés
- Tipo de recurso
- documento de conferencia
- Estado
- versión publicada
- Descripción
- The human apolipoprotein A-I (apoA-I) is the major protein component of high-density lipoproteins (HDL). It?s known that the interaction of apoA-I with macrophages trigger several signal transduction pathways. We realized a total proteomics profile between apoA-I and control treatment on THP-1 macrophages in order to find differential protein levels.To address if some unknown pathway could be activated by apoA-I we have analyzed a total proteomics profiling by comparative LFQ proteomics of apoA-I treated macrophages in comparison with untreated control.Total protein extracts were analyzed in a quadrupole/orbitrap. Subsequently, spectra were identified by two different software. Differential proteins levels were confirmed by Western-blot.Between 10 differentially-expressed proteins (at least in 2 folds over expressed on apoA-I-treated cells; p≤0.05) we found sequestrosome-1 (p62), a multifunctional protein that could be regulated by the Nrf2-KEAP1 pathway. When the Nrf2 pathway was inhibited by all-trans retinoic acid (ATRA), p62 levels decreases 40 to 50% in co treated cells (ATRA + ApoA-I) compared with only apoA-I-treated cells.We conclude that p62 could accumulates in THP-1-macrophages since apoA-I treatment in a Nrf2 pathway dependent manner.
Fil: Díaz Ludovico, Ivo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina
Fil: Trejo, Sebastian Alejandro. YPF - Tecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Becerra, Romina Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina
Fil: Garda, Horacio Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina
Fil: Gonzalez, Marina Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina
Vascular Discovery: From Genes to Medicine Scientific Sessions 2020
Estados Unidos
American Heart Association - Materia
-
apolipoprotein A-I
high-density lipoproteins
sequestrosome-1
THP-1-macrophages - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/278231
Ver los metadatos del registro completo
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Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 DependentDíaz Ludovico, IvoTrejo, Sebastian AlejandroBecerra, Romina ValeriaGarda, Horacio AlbertoGonzalez, Marina Ceciliaapolipoprotein A-Ihigh-density lipoproteinssequestrosome-1THP-1-macrophageshttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1The human apolipoprotein A-I (apoA-I) is the major protein component of high-density lipoproteins (HDL). It?s known that the interaction of apoA-I with macrophages trigger several signal transduction pathways. We realized a total proteomics profile between apoA-I and control treatment on THP-1 macrophages in order to find differential protein levels.To address if some unknown pathway could be activated by apoA-I we have analyzed a total proteomics profiling by comparative LFQ proteomics of apoA-I treated macrophages in comparison with untreated control.Total protein extracts were analyzed in a quadrupole/orbitrap. Subsequently, spectra were identified by two different software. Differential proteins levels were confirmed by Western-blot.Between 10 differentially-expressed proteins (at least in 2 folds over expressed on apoA-I-treated cells; p≤0.05) we found sequestrosome-1 (p62), a multifunctional protein that could be regulated by the Nrf2-KEAP1 pathway. When the Nrf2 pathway was inhibited by all-trans retinoic acid (ATRA), p62 levels decreases 40 to 50% in co treated cells (ATRA + ApoA-I) compared with only apoA-I-treated cells.We conclude that p62 could accumulates in THP-1-macrophages since apoA-I treatment in a Nrf2 pathway dependent manner.Fil: Díaz Ludovico, Ivo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; ArgentinaFil: Trejo, Sebastian Alejandro. YPF - Tecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Becerra, Romina Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; ArgentinaFil: Garda, Horacio Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; ArgentinaFil: Gonzalez, Marina Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; ArgentinaVascular Discovery: From Genes to Medicine Scientific Sessions 2020Estados UnidosAmerican Heart AssociationAmerican Heart Association2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectCongresoJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/mswordapplication/pdfhttp://hdl.handle.net/11336/278231Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent; Vascular Discovery: From Genes to Medicine Scientific Sessions 2020; Estados Unidos; 2020; 1-11079-5642CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1161/atvb.40.suppl_1.307info:eu-repo/semantics/altIdentifier/url/https://www.ahajournals.org/doi/10.1161/atvb.40.suppl_1.307Internacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-12-23T13:20:51Zoai:ri.conicet.gov.ar:11336/278231instacron: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:34982025-12-23 13:20:51.314CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| title |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| spellingShingle |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent Díaz Ludovico, Ivo apolipoprotein A-I high-density lipoproteins sequestrosome-1 THP-1-macrophages |
| title_short |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| title_full |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| title_fullStr |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| title_full_unstemmed |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| title_sort |
Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent |
| dc.creator.none.fl_str_mv |
Díaz Ludovico, Ivo Trejo, Sebastian Alejandro Becerra, Romina Valeria Garda, Horacio Alberto Gonzalez, Marina Cecilia |
| author |
Díaz Ludovico, Ivo |
| author_facet |
Díaz Ludovico, Ivo Trejo, Sebastian Alejandro Becerra, Romina Valeria Garda, Horacio Alberto Gonzalez, Marina Cecilia |
| author_role |
author |
| author2 |
Trejo, Sebastian Alejandro Becerra, Romina Valeria Garda, Horacio Alberto Gonzalez, Marina Cecilia |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
apolipoprotein A-I high-density lipoproteins sequestrosome-1 THP-1-macrophages |
| topic |
apolipoprotein A-I high-density lipoproteins sequestrosome-1 THP-1-macrophages |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
The human apolipoprotein A-I (apoA-I) is the major protein component of high-density lipoproteins (HDL). It?s known that the interaction of apoA-I with macrophages trigger several signal transduction pathways. We realized a total proteomics profile between apoA-I and control treatment on THP-1 macrophages in order to find differential protein levels.To address if some unknown pathway could be activated by apoA-I we have analyzed a total proteomics profiling by comparative LFQ proteomics of apoA-I treated macrophages in comparison with untreated control.Total protein extracts were analyzed in a quadrupole/orbitrap. Subsequently, spectra were identified by two different software. Differential proteins levels were confirmed by Western-blot.Between 10 differentially-expressed proteins (at least in 2 folds over expressed on apoA-I-treated cells; p≤0.05) we found sequestrosome-1 (p62), a multifunctional protein that could be regulated by the Nrf2-KEAP1 pathway. When the Nrf2 pathway was inhibited by all-trans retinoic acid (ATRA), p62 levels decreases 40 to 50% in co treated cells (ATRA + ApoA-I) compared with only apoA-I-treated cells.We conclude that p62 could accumulates in THP-1-macrophages since apoA-I treatment in a Nrf2 pathway dependent manner. Fil: Díaz Ludovico, Ivo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina Fil: Trejo, Sebastian Alejandro. YPF - Tecnología; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Becerra, Romina Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina Fil: Garda, Horacio Alberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina Fil: Gonzalez, Marina Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina Vascular Discovery: From Genes to Medicine Scientific Sessions 2020 Estados Unidos American Heart Association |
| description |
The human apolipoprotein A-I (apoA-I) is the major protein component of high-density lipoproteins (HDL). It?s known that the interaction of apoA-I with macrophages trigger several signal transduction pathways. We realized a total proteomics profile between apoA-I and control treatment on THP-1 macrophages in order to find differential protein levels.To address if some unknown pathway could be activated by apoA-I we have analyzed a total proteomics profiling by comparative LFQ proteomics of apoA-I treated macrophages in comparison with untreated control.Total protein extracts were analyzed in a quadrupole/orbitrap. Subsequently, spectra were identified by two different software. Differential proteins levels were confirmed by Western-blot.Between 10 differentially-expressed proteins (at least in 2 folds over expressed on apoA-I-treated cells; p≤0.05) we found sequestrosome-1 (p62), a multifunctional protein that could be regulated by the Nrf2-KEAP1 pathway. When the Nrf2 pathway was inhibited by all-trans retinoic acid (ATRA), p62 levels decreases 40 to 50% in co treated cells (ATRA + ApoA-I) compared with only apoA-I-treated cells.We conclude that p62 could accumulates in THP-1-macrophages since apoA-I treatment in a Nrf2 pathway dependent manner. |
| publishDate |
2020 |
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2020 |
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http://hdl.handle.net/11336/278231 Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent; Vascular Discovery: From Genes to Medicine Scientific Sessions 2020; Estados Unidos; 2020; 1-1 1079-5642 CONICET Digital CONICET |
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Apolipoprotein A-I Treatment on Thp1 Macrophages Result in the Accumulation of Sequestosome 1 (p62) via Nrf2 Dependent; Vascular Discovery: From Genes to Medicine Scientific Sessions 2020; Estados Unidos; 2020; 1-1 1079-5642 CONICET Digital CONICET |
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eng |
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info:eu-repo/semantics/altIdentifier/doi/10.1161/atvb.40.suppl_1.307 info:eu-repo/semantics/altIdentifier/url/https://www.ahajournals.org/doi/10.1161/atvb.40.suppl_1.307 |
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American Heart Association |
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American Heart Association |
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