NETosis Markers in Pregnancy: Effects Differ According to Histone Subtypes.


Journal

Thrombosis and haemostasis
ISSN: 2567-689X
Titre abrégé: Thromb Haemost
Pays: Germany
ID NLM: 7608063

Informations de publication

Date de publication:
Jul 2021
Historique:
pubmed: 11 1 2021
medline: 22 12 2021
entrez: 10 1 2021
Statut: ppublish

Résumé

NETosis is an innate immune response occurring after infection or inflammation: activated neutrophils expel decondensed DNA in complex with histones into the extracellular environment in a controlled manner. It activates coagulation and fuels the risk of thrombosis. Human pregnancy is associated with a mild proinflammatory state characterized by circulatory neutrophil activation which is further increased in complicated pregnancies, placenta-mediated complications being associated with an increased thrombotic risk. This aberrant activation leads to an increased release of nucleosomes in the blood flow. The aim of our study was to initially quantify nucleosome-bound histones in normal pregnancy and in placenta-mediated complication counterpart. We analyzed the role of histones on extravillous trophoblast function. Circulating nucleosome-bound histones H3 (Nu.QH3.1, Nu.QH3PanCit, Nu.QH3K27me3) and H4 (Nu.QH4K16Ac) were increased in complicated pregnancies. In vitro using the extravillous cell line HTR-8/SVNeo, we observed that free recombinant H2B, H3, and H4 inhibited migration in wound healing assay, but only H3 also blocked invasion in Matrigel-coated Transwell experiments. H3 and H4 also induced apoptosis, whereas H2B did not. Finally, the negative effects of H3 on invasion and apoptosis could be restored with enoxaparin, a low-molecular-weight heparin (LMWH), but not with aspirin. Different circulating nucleosome-bound histones are increased in complicated pregnancy and this would affect migration, invasion, and induce apoptosis of extravillous trophoblasts. Histones might be part of the link between the risk of thrombosis and pregnancy complications, with an effect of LMWH on both.

Identifiants

pubmed: 33423243
doi: 10.1055/s-0040-1722225
doi:

Substances chimiques

Enoxaparin 0
Heparin, Low-Molecular-Weight 0
Histones 0
Nucleosomes 0
Aspirin R16CO5Y76E

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

877-890

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

S. Bouvier, M. Fortier, L. Vincent, C. Demattei, E. Mousty, E. Nouvellon, E. Mercier, V. Letouzey, and J.-C. Gris report no conflict of interest related to this manuscript. M. Herzog and G. Rommelaere are employees of Belgian Volition SPRL Company.

Auteurs

Sylvie Bouvier (S)

Department of Haematology, University Hospital, Nîmes, France.
Research Laboratory EA 2992, Montpellier University, Montpellier, France.
Faculty of Pharmaceutical and Biological Sciences, Montpellier University, Montpellier, France.

Mathieu Fortier (M)

Department of Haematology, University Hospital, Nîmes, France.

Laura Vincent (L)

Department of Haematology, University Hospital, Nîmes, France.

Christophe Demattei (C)

Department of Biostatistics, Public Health and Innovation in Methodology, Nîmes University Hospital, Nîmes, France.

Eve Mousty (E)

Department of Gynecology and Obstetrics, University Hospital, Nîmes, France.

Marielle Herzog (M)

Belgian Volition SPRL, Parc Scientifique Crealys, Isnes, Belgium.

Guillaume Rommelaere (G)

Belgian Volition SPRL, Parc Scientifique Crealys, Isnes, Belgium.

Eva Nouvellon (E)

Department of Haematology, University Hospital, Nîmes, France.
Research Laboratory EA 2992, Montpellier University, Montpellier, France.

Eric Mercier (E)

Department of Haematology, University Hospital, Nîmes, France.
Research Laboratory EA 2992, Montpellier University, Montpellier, France.
Faculty of Pharmaceutical and Biological Sciences, Montpellier University, Montpellier, France.

Vincent Letouzey (V)

Department of Gynecology and Obstetrics, University Hospital, Nîmes, France.
Department of Artificial Polymers, Max Mousseron Institute of Biomolecules, Montpellier University, Montpellier, France.

Jean-Christophe Gris (JC)

Department of Haematology, University Hospital, Nîmes, France.
Research Laboratory EA 2992, Montpellier University, Montpellier, France.
Faculty of Pharmaceutical and Biological Sciences, Montpellier University, Montpellier, France.
Department of Gynecology, I. M. Sechenov First Moscow State Medical University, Moscow, Russian Federation.

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Classifications MeSH