Cargando…

Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation

Extracellular vesicles released by the primary pathogen of periodontal disease Porphyromonas gingivalis (Pg), referred to as outer membrane vesicles (OMVs), have been associated with the pathogenesis of systemic diseases like cardiovascular disease, rheumatoid arthritis, and Alzheimer’s disease. A p...

Descripción completa

Detalles Bibliográficos
Autores principales: Lara, Brenda, Sassot, Matías, Calo, Guillermina, Paparini, Daniel, Gliosca, Laura, Chaufan, Gabriela, Loureiro, Iñaki, Vota, Daiana, Ramhorst, Rosanna, Pérez Leirós, Claudia, Hauk, Vanesa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10608595/
https://www.ncbi.nlm.nih.gov/pubmed/37895353
http://dx.doi.org/10.3390/life13101971
_version_ 1785127817446424576
author Lara, Brenda
Sassot, Matías
Calo, Guillermina
Paparini, Daniel
Gliosca, Laura
Chaufan, Gabriela
Loureiro, Iñaki
Vota, Daiana
Ramhorst, Rosanna
Pérez Leirós, Claudia
Hauk, Vanesa
author_facet Lara, Brenda
Sassot, Matías
Calo, Guillermina
Paparini, Daniel
Gliosca, Laura
Chaufan, Gabriela
Loureiro, Iñaki
Vota, Daiana
Ramhorst, Rosanna
Pérez Leirós, Claudia
Hauk, Vanesa
author_sort Lara, Brenda
collection PubMed
description Extracellular vesicles released by the primary pathogen of periodontal disease Porphyromonas gingivalis (Pg), referred to as outer membrane vesicles (OMVs), have been associated with the pathogenesis of systemic diseases like cardiovascular disease, rheumatoid arthritis, and Alzheimer’s disease. A pathogenic role for Pg by disrupting placental homeostasis was proposed in the association between periodontal disease and adverse pregnancy outcomes. On the basis that trophoblast-derived factors modulate endothelial and immune cell profiles in normal pregnancy and the scarce presence of Pg in placenta, we hypothesized that OMVs from Pg affect trophoblast cell phenotype, impairing trophoblast–endothelium and trophoblast–neutrophil interactions. By means of in vitro designs with first-trimester human trophoblast cells, endothelial cells, and freshly isolated neutrophils, we showed that Pg OMVs are internalized by trophoblast cells and modulate the activity and expression of functional markers. Trophoblast cells primed with Pg OMVs enhanced neutrophil chemoattraction and lost their anti-inflammatory effect. In addition, reduced migration with enhanced adhesion of monocytes was found in endothelial cells upon incubation with the media from trophoblast cells pretreated with Pg OMVs. Taken together, the results support a pathogenic role of Pg OMVs at early stages of pregnancy and placentation through disruption of trophoblast contribution to vascular transformation and immune homeostasis maintenance.
format Online
Article
Text
id pubmed-10608595
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-106085952023-10-28 Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation Lara, Brenda Sassot, Matías Calo, Guillermina Paparini, Daniel Gliosca, Laura Chaufan, Gabriela Loureiro, Iñaki Vota, Daiana Ramhorst, Rosanna Pérez Leirós, Claudia Hauk, Vanesa Life (Basel) Article Extracellular vesicles released by the primary pathogen of periodontal disease Porphyromonas gingivalis (Pg), referred to as outer membrane vesicles (OMVs), have been associated with the pathogenesis of systemic diseases like cardiovascular disease, rheumatoid arthritis, and Alzheimer’s disease. A pathogenic role for Pg by disrupting placental homeostasis was proposed in the association between periodontal disease and adverse pregnancy outcomes. On the basis that trophoblast-derived factors modulate endothelial and immune cell profiles in normal pregnancy and the scarce presence of Pg in placenta, we hypothesized that OMVs from Pg affect trophoblast cell phenotype, impairing trophoblast–endothelium and trophoblast–neutrophil interactions. By means of in vitro designs with first-trimester human trophoblast cells, endothelial cells, and freshly isolated neutrophils, we showed that Pg OMVs are internalized by trophoblast cells and modulate the activity and expression of functional markers. Trophoblast cells primed with Pg OMVs enhanced neutrophil chemoattraction and lost their anti-inflammatory effect. In addition, reduced migration with enhanced adhesion of monocytes was found in endothelial cells upon incubation with the media from trophoblast cells pretreated with Pg OMVs. Taken together, the results support a pathogenic role of Pg OMVs at early stages of pregnancy and placentation through disruption of trophoblast contribution to vascular transformation and immune homeostasis maintenance. MDPI 2023-09-27 /pmc/articles/PMC10608595/ /pubmed/37895353 http://dx.doi.org/10.3390/life13101971 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lara, Brenda
Sassot, Matías
Calo, Guillermina
Paparini, Daniel
Gliosca, Laura
Chaufan, Gabriela
Loureiro, Iñaki
Vota, Daiana
Ramhorst, Rosanna
Pérez Leirós, Claudia
Hauk, Vanesa
Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation
title Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation
title_full Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation
title_fullStr Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation
title_full_unstemmed Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation
title_short Extracellular Vesicles of Porphyromonas gingivalis Disrupt Trophoblast Cell Interaction with Vascular and Immune Cells in an In Vitro Model of Early Placentation
title_sort extracellular vesicles of porphyromonas gingivalis disrupt trophoblast cell interaction with vascular and immune cells in an in vitro model of early placentation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10608595/
https://www.ncbi.nlm.nih.gov/pubmed/37895353
http://dx.doi.org/10.3390/life13101971
work_keys_str_mv AT larabrenda extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT sassotmatias extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT caloguillermina extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT paparinidaniel extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT glioscalaura extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT chaufangabriela extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT loureiroinaki extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT votadaiana extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT ramhorstrosanna extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT perezleirosclaudia extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation
AT haukvanesa extracellularvesiclesofporphyromonasgingivalisdisrupttrophoblastcellinteractionwithvascularandimmunecellsinaninvitromodelofearlyplacentation