Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox?
ABSTRACT: Antiphospholipid antibodies (aPL) lead to a hypercoagulable state in vivo. Paradoxically, some of these autoantibodies perform as inhibitors of the coagulation cascade in vitro (a phenomenon referred to as “lupus anticoagulant”). The presence of lupus anticoagulant has been related to an i...
- Autores:
-
Álvarez Jaramillo, Daniel
Rúa Molina, Diana Carolina
Velásquez Berrío, Manuela
Cataño Bedoya, John Ubeimar
Escudero, Carlos Alonso
Cadavid Jaramillo, Ángela Patricia
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2022
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/31499
- Acceso en línea:
- https://hdl.handle.net/10495/31499
- Palabra clave:
- Anticuerpos Antifosfolípidos
Antibodies, Antiphospholipid
Inhibidor de Coagulación del Lupus
Lupus Coagulation Inhibitor
Quinasas de Proteína Quinasa Activadas por Mitógenos
Mitogen-Activated Protein Kinase Kinases
Síndrome Antifosfolípido
Antiphospholipid Syndrome
Trombosis
Thrombosis
Vesículas Extracelulares
Extracellular Vesicles
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-nd/4.0/
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Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| title |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| spellingShingle |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? Anticuerpos Antifosfolípidos Antibodies, Antiphospholipid Inhibidor de Coagulación del Lupus Lupus Coagulation Inhibitor Quinasas de Proteína Quinasa Activadas por Mitógenos Mitogen-Activated Protein Kinase Kinases Síndrome Antifosfolípido Antiphospholipid Syndrome Trombosis Thrombosis Vesículas Extracelulares Extracellular Vesicles |
| title_short |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| title_full |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| title_fullStr |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| title_full_unstemmed |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| title_sort |
Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? |
| dc.creator.fl_str_mv |
Álvarez Jaramillo, Daniel Rúa Molina, Diana Carolina Velásquez Berrío, Manuela Cataño Bedoya, John Ubeimar Escudero, Carlos Alonso Cadavid Jaramillo, Ángela Patricia |
| dc.contributor.author.none.fl_str_mv |
Álvarez Jaramillo, Daniel Rúa Molina, Diana Carolina Velásquez Berrío, Manuela Cataño Bedoya, John Ubeimar Escudero, Carlos Alonso Cadavid Jaramillo, Ángela Patricia |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo de Investigación en Trombosis Grupo Reproducción |
| dc.subject.decs.none.fl_str_mv |
Anticuerpos Antifosfolípidos Antibodies, Antiphospholipid Inhibidor de Coagulación del Lupus Lupus Coagulation Inhibitor Quinasas de Proteína Quinasa Activadas por Mitógenos Mitogen-Activated Protein Kinase Kinases Síndrome Antifosfolípido Antiphospholipid Syndrome Trombosis Thrombosis Vesículas Extracelulares Extracellular Vesicles |
| topic |
Anticuerpos Antifosfolípidos Antibodies, Antiphospholipid Inhibidor de Coagulación del Lupus Lupus Coagulation Inhibitor Quinasas de Proteína Quinasa Activadas por Mitógenos Mitogen-Activated Protein Kinase Kinases Síndrome Antifosfolípido Antiphospholipid Syndrome Trombosis Thrombosis Vesículas Extracelulares Extracellular Vesicles |
| description |
ABSTRACT: Antiphospholipid antibodies (aPL) lead to a hypercoagulable state in vivo. Paradoxically, some of these autoantibodies perform as inhibitors of the coagulation cascade in vitro (a phenomenon referred to as “lupus anticoagulant”). The presence of lupus anticoagulant has been related to an increased quantity of plasma extracellular vesicles, which may constitute a direct procoagulant mechanism in antiphospholipid syndrome. This study investigates whether or not endothelial cell-derived extracellular vesicles released upon stimulation with aPL (aPL-EDEVs) are related to a higher direct coagulation activity. Using an in vitro model of endothelium, flow cytometry and a recalcified plasma-based assay, we found that the coagulation activity of aPL-EDEVs is mainly conditioned by the lupus anticoagulant-like activity of autoantibodies. Nevertheless, in the presence of β2 glycoprotein I, a cofactor of aPL during the stimulation of endothelial cells, the coagulation activity of EDEVs is restored in a mitogen-activated protein kinase kinases 1 and 2 (MEK1/2)-dependent manner. This phenomenon was especially evident when using immunoglobulins G from patients with vascular and obstetric primary antiphospholipid syndrome who manifest refractoriness to treatment. Our findings suggest that the role of aPL-EDEVs in the antiphospholipid syndrome-related hypercoagulable state may not rely on their capacity to enhance clotting directly. While β2 glycoprotein I performs as a procoagulant cofactor and restores the coagulation activity of extracellular vesicles via MEK1/2 pathway, proportionally, autoantibodies interact with aPL-EDEVs and exhaust their coagulation properties. Further analysis is required to establish whether lupus anticoagulant-like autoantibodies opsonise extracellular vesicles and whether opsonised vesicles may lead to thrombosis by indirect means. |
| publishDate |
2022 |
| dc.date.accessioned.none.fl_str_mv |
2022-10-27T17:25:24Z |
| dc.date.available.none.fl_str_mv |
2022-10-27T17:25:24Z |
| dc.date.issued.none.fl_str_mv |
2022 |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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Álvarez D, Rúa C, Velásquez Berrío M, Cataño JU, Escudero C, Cadavid J ÁP. Extracellular vesicles released upon stimulation with antiphospholipid antibodies: An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? J Autoimmun. 2022 Sep 15;133:102905. doi: 10.1016/j.jaut.2022.102905. Epub ahead of print. PMID: 36115210. |
| dc.identifier.issn.none.fl_str_mv |
0896-8411 |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/31499 |
| dc.identifier.doi.none.fl_str_mv |
10.1016/j.jaut.2022.102905 |
| dc.identifier.eissn.none.fl_str_mv |
1095-9157 |
| identifier_str_mv |
Álvarez D, Rúa C, Velásquez Berrío M, Cataño JU, Escudero C, Cadavid J ÁP. Extracellular vesicles released upon stimulation with antiphospholipid antibodies: An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? J Autoimmun. 2022 Sep 15;133:102905. doi: 10.1016/j.jaut.2022.102905. Epub ahead of print. PMID: 36115210. 0896-8411 10.1016/j.jaut.2022.102905 1095-9157 |
| url |
https://hdl.handle.net/10495/31499 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
J. Autoimmun. |
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12 |
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1 |
| dc.relation.citationvolume.spa.fl_str_mv |
133 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Journal of Autoimmunity |
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https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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Elsevier |
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Londres, Inglaterra |
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Álvarez Jaramillo, DanielRúa Molina, Diana CarolinaVelásquez Berrío, ManuelaCataño Bedoya, John UbeimarEscudero, Carlos AlonsoCadavid Jaramillo, Ángela PatriciaGrupo de Investigación en TrombosisGrupo Reproducción2022-10-27T17:25:24Z2022-10-27T17:25:24Z2022Álvarez D, Rúa C, Velásquez Berrío M, Cataño JU, Escudero C, Cadavid J ÁP. Extracellular vesicles released upon stimulation with antiphospholipid antibodies: An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox? J Autoimmun. 2022 Sep 15;133:102905. doi: 10.1016/j.jaut.2022.102905. Epub ahead of print. PMID: 36115210.0896-8411https://hdl.handle.net/10495/3149910.1016/j.jaut.2022.1029051095-9157ABSTRACT: Antiphospholipid antibodies (aPL) lead to a hypercoagulable state in vivo. Paradoxically, some of these autoantibodies perform as inhibitors of the coagulation cascade in vitro (a phenomenon referred to as “lupus anticoagulant”). The presence of lupus anticoagulant has been related to an increased quantity of plasma extracellular vesicles, which may constitute a direct procoagulant mechanism in antiphospholipid syndrome. This study investigates whether or not endothelial cell-derived extracellular vesicles released upon stimulation with aPL (aPL-EDEVs) are related to a higher direct coagulation activity. Using an in vitro model of endothelium, flow cytometry and a recalcified plasma-based assay, we found that the coagulation activity of aPL-EDEVs is mainly conditioned by the lupus anticoagulant-like activity of autoantibodies. Nevertheless, in the presence of β2 glycoprotein I, a cofactor of aPL during the stimulation of endothelial cells, the coagulation activity of EDEVs is restored in a mitogen-activated protein kinase kinases 1 and 2 (MEK1/2)-dependent manner. This phenomenon was especially evident when using immunoglobulins G from patients with vascular and obstetric primary antiphospholipid syndrome who manifest refractoriness to treatment. Our findings suggest that the role of aPL-EDEVs in the antiphospholipid syndrome-related hypercoagulable state may not rely on their capacity to enhance clotting directly. While β2 glycoprotein I performs as a procoagulant cofactor and restores the coagulation activity of extracellular vesicles via MEK1/2 pathway, proportionally, autoantibodies interact with aPL-EDEVs and exhaust their coagulation properties. Further analysis is required to establish whether lupus anticoagulant-like autoantibodies opsonise extracellular vesicles and whether opsonised vesicles may lead to thrombosis by indirect means.COL0007631COL001042112application/pdfengElsevierLondres, Inglaterrahttps://creativecommons.org/licenses/by-nc-nd/4.0/http://creativecommons.org/licenses/by-nc-nd/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Extracellular vesicles released upon stimulation with antiphospholipid antibodies : An actual direct procoagulant mechanism or a new factor in the lupus anticoagulant paradox?Artículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAnticuerpos AntifosfolípidosAntibodies, AntiphospholipidInhibidor de Coagulación del LupusLupus Coagulation InhibitorQuinasas de Proteína Quinasa Activadas por MitógenosMitogen-Activated Protein Kinase KinasesSíndrome AntifosfolípidoAntiphospholipid SyndromeTrombosisThrombosisVesículas ExtracelularesExtracellular VesiclesJ. 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