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Neutrophil migration into the placenta: Good, bad or deadly?
Almost 2 decades have passed since the discovery that pregnancy is associated with a basal inflammatory state involving neutrophil activation, and that this is more overt in cases with preeclampsia, than in instances with sepsis. This pivotal observation paved the way for our report, made almost a d...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853040/ https://www.ncbi.nlm.nih.gov/pubmed/26933824 http://dx.doi.org/10.1080/19336918.2016.1148866 |
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author | Giaglis, Stavros Stoikou, Maria Grimolizzi, Franco Subramanian, Bibin Y. van Breda, Shane V. Hoesli, Irene Lapaire, Olav Hasler, Paul Than, Nandor Gabor Hahn, Sinuhe |
author_facet | Giaglis, Stavros Stoikou, Maria Grimolizzi, Franco Subramanian, Bibin Y. van Breda, Shane V. Hoesli, Irene Lapaire, Olav Hasler, Paul Than, Nandor Gabor Hahn, Sinuhe |
author_sort | Giaglis, Stavros |
collection | PubMed |
description | Almost 2 decades have passed since the discovery that pregnancy is associated with a basal inflammatory state involving neutrophil activation, and that this is more overt in cases with preeclampsia, than in instances with sepsis. This pivotal observation paved the way for our report, made almost a decade ago, describing the first involvement of neutrophil extracellular traps (NETs) in a non-infectious human pathology, namely preeclampsia, where an abundance of these structures were detected directly in the placental intervillous space. Despite these remarkable findings, there remains a paucity of interest among reproductive biologists in further exploring the role or involvement of neutrophils in pregnancy and related pathologies. In this review we attempt to redress this deficit by highlighting novel recent findings including the discovery of a novel neutrophil subset in the decidua, the interaction of placental protein 13 (PP13) and neutrophils in modulating spiral artery modification, as well as the use of animal model systems to elucidate neutrophil function in implantation, gestation and parturition. These model systems have been particularly useful in identifying key components implicated in recurrent fetal loss, preeclampsia or new signaling molecules such as sphingolipids. Finally, the recent discovery that anti-phospolipid antibodies can trigger NETosis, supports our hypothesis that these structures may contribute to placental dysfunction in pertinent cases with recurrent fetal loss. |
format | Online Article Text |
id | pubmed-4853040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-48530402016-05-10 Neutrophil migration into the placenta: Good, bad or deadly? Giaglis, Stavros Stoikou, Maria Grimolizzi, Franco Subramanian, Bibin Y. van Breda, Shane V. Hoesli, Irene Lapaire, Olav Hasler, Paul Than, Nandor Gabor Hahn, Sinuhe Cell Adh Migr Review Almost 2 decades have passed since the discovery that pregnancy is associated with a basal inflammatory state involving neutrophil activation, and that this is more overt in cases with preeclampsia, than in instances with sepsis. This pivotal observation paved the way for our report, made almost a decade ago, describing the first involvement of neutrophil extracellular traps (NETs) in a non-infectious human pathology, namely preeclampsia, where an abundance of these structures were detected directly in the placental intervillous space. Despite these remarkable findings, there remains a paucity of interest among reproductive biologists in further exploring the role or involvement of neutrophils in pregnancy and related pathologies. In this review we attempt to redress this deficit by highlighting novel recent findings including the discovery of a novel neutrophil subset in the decidua, the interaction of placental protein 13 (PP13) and neutrophils in modulating spiral artery modification, as well as the use of animal model systems to elucidate neutrophil function in implantation, gestation and parturition. These model systems have been particularly useful in identifying key components implicated in recurrent fetal loss, preeclampsia or new signaling molecules such as sphingolipids. Finally, the recent discovery that anti-phospolipid antibodies can trigger NETosis, supports our hypothesis that these structures may contribute to placental dysfunction in pertinent cases with recurrent fetal loss. Taylor & Francis 2016-03-02 /pmc/articles/PMC4853040/ /pubmed/26933824 http://dx.doi.org/10.1080/19336918.2016.1148866 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Review Giaglis, Stavros Stoikou, Maria Grimolizzi, Franco Subramanian, Bibin Y. van Breda, Shane V. Hoesli, Irene Lapaire, Olav Hasler, Paul Than, Nandor Gabor Hahn, Sinuhe Neutrophil migration into the placenta: Good, bad or deadly? |
title | Neutrophil migration into the placenta: Good, bad or deadly? |
title_full | Neutrophil migration into the placenta: Good, bad or deadly? |
title_fullStr | Neutrophil migration into the placenta: Good, bad or deadly? |
title_full_unstemmed | Neutrophil migration into the placenta: Good, bad or deadly? |
title_short | Neutrophil migration into the placenta: Good, bad or deadly? |
title_sort | neutrophil migration into the placenta: good, bad or deadly? |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853040/ https://www.ncbi.nlm.nih.gov/pubmed/26933824 http://dx.doi.org/10.1080/19336918.2016.1148866 |
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