Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells

ABSTRACT: In systemic lupus erythematosus (SLE), the clearance of apoptotic cells and microparticles (MPs) is reduced. Some MPs contain molecules that can modulate immune responses. This study aimed to evaluate the presence of miR-126 and miR-146a in plasma MPs of patients with SLE (SLE MPs) and ana...

Full description

Autores:
Carmona Pérez, Liseth
Rojas López, Mauricio
Muñoz Vahos, Carlos
Vanegas García, Adiana
Vásquez Duque, Gloria María
Tipo de recurso:
Article of investigation
Fecha de publicación:
2021
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/43707
Acceso en línea:
https://hdl.handle.net/10495/43707
https://onlinelibrary.wiley.com/doi/10.1111/imm.13366
Palabra clave:
MicroARNs
MicroRNAs
Lupus Eritematoso Sistémico
Lupus Erythematosus, Systemic
Micropartículas Derivadas de Células - Metabolismo
Cell-Derived Microparticles - Metabolism
Células U937
U937 Cells
Inmunidad
Immunity
Enfermedades Autoinmunes
Autoimmune Diseases
https://id.nlm.nih.gov/mesh/D035683
https://id.nlm.nih.gov/mesh/D008180
https://id.nlm.nih.gov/mesh/D055252
https://id.nlm.nih.gov/mesh/D020298
https://id.nlm.nih.gov/mesh/D007109
https://id.nlm.nih.gov/mesh/D001327
Rights
openAccess
License
http://creativecommons.org/licenses/by-nc-nd/2.5/co/
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oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/43707
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
title Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
spellingShingle Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
MicroARNs
MicroRNAs
Lupus Eritematoso Sistémico
Lupus Erythematosus, Systemic
Micropartículas Derivadas de Células - Metabolismo
Cell-Derived Microparticles - Metabolism
Células U937
U937 Cells
Inmunidad
Immunity
Enfermedades Autoinmunes
Autoimmune Diseases
https://id.nlm.nih.gov/mesh/D035683
https://id.nlm.nih.gov/mesh/D008180
https://id.nlm.nih.gov/mesh/D055252
https://id.nlm.nih.gov/mesh/D020298
https://id.nlm.nih.gov/mesh/D007109
https://id.nlm.nih.gov/mesh/D001327
title_short Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
title_full Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
title_fullStr Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
title_full_unstemmed Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
title_sort Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells
dc.creator.fl_str_mv Carmona Pérez, Liseth
Rojas López, Mauricio
Muñoz Vahos, Carlos
Vanegas García, Adiana
Vásquez Duque, Gloria María
dc.contributor.author.none.fl_str_mv Carmona Pérez, Liseth
Rojas López, Mauricio
Muñoz Vahos, Carlos
Vanegas García, Adiana
Vásquez Duque, Gloria María
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Inmunología Celular e Inmunogenética
Grupo de Reumatología Universidad de Antioquia -GRUA-
dc.subject.decs.none.fl_str_mv MicroARNs
MicroRNAs
Lupus Eritematoso Sistémico
Lupus Erythematosus, Systemic
Micropartículas Derivadas de Células - Metabolismo
Cell-Derived Microparticles - Metabolism
Células U937
U937 Cells
Inmunidad
Immunity
Enfermedades Autoinmunes
Autoimmune Diseases
topic MicroARNs
MicroRNAs
Lupus Eritematoso Sistémico
Lupus Erythematosus, Systemic
Micropartículas Derivadas de Células - Metabolismo
Cell-Derived Microparticles - Metabolism
Células U937
U937 Cells
Inmunidad
Immunity
Enfermedades Autoinmunes
Autoimmune Diseases
https://id.nlm.nih.gov/mesh/D035683
https://id.nlm.nih.gov/mesh/D008180
https://id.nlm.nih.gov/mesh/D055252
https://id.nlm.nih.gov/mesh/D020298
https://id.nlm.nih.gov/mesh/D007109
https://id.nlm.nih.gov/mesh/D001327
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D035683
https://id.nlm.nih.gov/mesh/D008180
https://id.nlm.nih.gov/mesh/D055252
https://id.nlm.nih.gov/mesh/D020298
https://id.nlm.nih.gov/mesh/D007109
https://id.nlm.nih.gov/mesh/D001327
description ABSTRACT: In systemic lupus erythematosus (SLE), the clearance of apoptotic cells and microparticles (MPs) is reduced. Some MPs contain molecules that can modulate immune responses. This study aimed to evaluate the presence of miR-126 and miR-146a in plasma MPs of patients with SLE (SLE MPs) and analyse the ability of MPs to modulate some events in the promonocytic U937 cell line. Circulating MPs were isolated from plasma samples of healthy controls (HCs), patients with SLE and other autoimmune diseases (OAD). MPs were analysed for size and cell origin by flow cytometry and content of miR-126 and miR-146a by RT-qPCR. MPs were then added to U937 cell cultures to evaluate changes in cell phenotype, cytokine expression, content of miR-126 and miR-146a, and levels of IRF5. Patients with active SLE (aSLE) showed an increase in concentration of plasma MPs that positively correlated with the SLEDAI (SLE Disease Activity Index) score. CD14+ MPs were significantly more abundant in patients with SLE than HCs. SLE MPs contained decreased levels of miR-146a, but the miR-126 content in aSLE MPs was increased. The miR-126 content in SLE MPs correlated positively with the SLEDAI score. The treatment of U937 cells with MPs from HCs and patients induced reduced expression of HLA-DR, CD18 and CD119, increased frequency of IL-6+ and TNF-α+ cells, accumulation of IL-8 in culture supernatants, increased miR-126 levels and decreased miR-146a content, but no change in the expression of IRF5. These findings suggest that plasma MPs, especially SLE MPs, could modulate some biological events in U937 cells.
publishDate 2021
dc.date.issued.none.fl_str_mv 2021
dc.date.accessioned.none.fl_str_mv 2024-11-22T20:50:14Z
dc.date.available.none.fl_str_mv 2024-11-22T20:50:14Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.citation.spa.fl_str_mv Carmona-Pérez L, Rojas M, Muñoz-Vahos C, Vanegas-García A, Vásquez G. Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells. Immunology. 2021 Oct;164(2):253-265. doi: 10.1111/imm.13366.
dc.identifier.issn.none.fl_str_mv 0019-2805
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/43707
dc.identifier.doi.none.fl_str_mv doi.org/10.1111/imm.13366
dc.identifier.eissn.none.fl_str_mv 1365-2567
dc.identifier.url.spa.fl_str_mv https://onlinelibrary.wiley.com/doi/10.1111/imm.13366
identifier_str_mv Carmona-Pérez L, Rojas M, Muñoz-Vahos C, Vanegas-García A, Vásquez G. Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells. Immunology. 2021 Oct;164(2):253-265. doi: 10.1111/imm.13366.
0019-2805
doi.org/10.1111/imm.13366
1365-2567
url https://hdl.handle.net/10495/43707
https://onlinelibrary.wiley.com/doi/10.1111/imm.13366
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Immunology.
dc.relation.citationendpage.spa.fl_str_mv 265
dc.relation.citationissue.spa.fl_str_mv 2
dc.relation.citationstartpage.spa.fl_str_mv 253
dc.relation.citationvolume.spa.fl_str_mv 164
dc.relation.ispartofjournal.spa.fl_str_mv Immunology
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/2.5/co/
dc.rights.uri.spa.fl_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.accessrights.spa.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.extent.spa.fl_str_mv 13 páginas
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dc.publisher.spa.fl_str_mv Wiley
dc.publisher.place.spa.fl_str_mv Oxford, Inglaterra
institution Universidad de Antioquia
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spelling Carmona Pérez, LisethRojas López, MauricioMuñoz Vahos, CarlosVanegas García, AdianaVásquez Duque, Gloria MaríaGrupo de Inmunología Celular e InmunogenéticaGrupo de Reumatología Universidad de Antioquia -GRUA-2024-11-22T20:50:14Z2024-11-22T20:50:14Z2021Carmona-Pérez L, Rojas M, Muñoz-Vahos C, Vanegas-García A, Vásquez G. Plasma microparticles from patients with systemic lupus erythematosus modulate the content of miRNAs in U937 cells. Immunology. 2021 Oct;164(2):253-265. doi: 10.1111/imm.13366.0019-2805https://hdl.handle.net/10495/43707doi.org/10.1111/imm.133661365-2567https://onlinelibrary.wiley.com/doi/10.1111/imm.13366ABSTRACT: In systemic lupus erythematosus (SLE), the clearance of apoptotic cells and microparticles (MPs) is reduced. Some MPs contain molecules that can modulate immune responses. This study aimed to evaluate the presence of miR-126 and miR-146a in plasma MPs of patients with SLE (SLE MPs) and analyse the ability of MPs to modulate some events in the promonocytic U937 cell line. Circulating MPs were isolated from plasma samples of healthy controls (HCs), patients with SLE and other autoimmune diseases (OAD). MPs were analysed for size and cell origin by flow cytometry and content of miR-126 and miR-146a by RT-qPCR. MPs were then added to U937 cell cultures to evaluate changes in cell phenotype, cytokine expression, content of miR-126 and miR-146a, and levels of IRF5. Patients with active SLE (aSLE) showed an increase in concentration of plasma MPs that positively correlated with the SLEDAI (SLE Disease Activity Index) score. CD14+ MPs were significantly more abundant in patients with SLE than HCs. SLE MPs contained decreased levels of miR-146a, but the miR-126 content in aSLE MPs was increased. The miR-126 content in SLE MPs correlated positively with the SLEDAI score. The treatment of U937 cells with MPs from HCs and patients induced reduced expression of HLA-DR, CD18 and CD119, increased frequency of IL-6+ and TNF-α+ cells, accumulation of IL-8 in culture supernatants, increased miR-126 levels and decreased miR-146a content, but no change in the expression of IRF5. These findings suggest that plasma MPs, especially SLE MPs, could modulate some biological events in U937 cells.Colombia. 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