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Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5

During the establishment of pregnancy, extravillous trophoblast (EVT) must invade into the uterine decidua to facilitate decidual artery remodelling to create the placental blood supply. The local decidual environment is thought to regulate trophoblast invasion, however these interactions are poorly...

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Autores principales: Menkhorst, E. M., Van Sinderen, M. L., Rainczuk, K., Cuman, C., Winship, A., Dimitriadis, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562808/
https://www.ncbi.nlm.nih.gov/pubmed/28821715
http://dx.doi.org/10.1038/s41598-017-05947-0
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author Menkhorst, E. M.
Van Sinderen, M. L.
Rainczuk, K.
Cuman, C.
Winship, A.
Dimitriadis, E.
author_facet Menkhorst, E. M.
Van Sinderen, M. L.
Rainczuk, K.
Cuman, C.
Winship, A.
Dimitriadis, E.
author_sort Menkhorst, E. M.
collection PubMed
description During the establishment of pregnancy, extravillous trophoblast (EVT) must invade into the uterine decidua to facilitate decidual artery remodelling to create the placental blood supply. The local decidual environment is thought to regulate trophoblast invasion, however these interactions are poorly defined in humans. Recent evidence in women suggests impaired decidualization is associated with miscarriage and preeclampsia. Primary human endometrial stromal cells (HESC) and first trimester extravillous trophoblast (EVTs) were used to assess the effect of EVT-secreted factors on HESC decidualization, adhesion, proliferation and migration. We determined the role of profilin (PFN)1, an EVT-secreted factor, on HESC function and identified a downstream target of PFN1. EVT-secreted factors induced HESC decidualization and enhanced decidualized HESC adhesion, proliferation and migration. Recombinant PFN1 enhanced methoxyprogesterone acetate-induced HESC decidualization and proliferation. PFN1 down-regulated the expression of lipoxygenase arachidonate 5-lipoxygenase (ALOX5) in HESC and THP-1 macrophages. ALOX5 localised to decidual cells and CD68+macrophages in 1(st) trimester decidua. This study demonstrated that EVT secretions, including PFN1, enhanced HESC decidualization and motility. This study has identified a new pathway that facilitates appropriate decidualization during the establishment of pregnancy.
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spelling pubmed-55628082017-08-21 Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5 Menkhorst, E. M. Van Sinderen, M. L. Rainczuk, K. Cuman, C. Winship, A. Dimitriadis, E. Sci Rep Article During the establishment of pregnancy, extravillous trophoblast (EVT) must invade into the uterine decidua to facilitate decidual artery remodelling to create the placental blood supply. The local decidual environment is thought to regulate trophoblast invasion, however these interactions are poorly defined in humans. Recent evidence in women suggests impaired decidualization is associated with miscarriage and preeclampsia. Primary human endometrial stromal cells (HESC) and first trimester extravillous trophoblast (EVTs) were used to assess the effect of EVT-secreted factors on HESC decidualization, adhesion, proliferation and migration. We determined the role of profilin (PFN)1, an EVT-secreted factor, on HESC function and identified a downstream target of PFN1. EVT-secreted factors induced HESC decidualization and enhanced decidualized HESC adhesion, proliferation and migration. Recombinant PFN1 enhanced methoxyprogesterone acetate-induced HESC decidualization and proliferation. PFN1 down-regulated the expression of lipoxygenase arachidonate 5-lipoxygenase (ALOX5) in HESC and THP-1 macrophages. ALOX5 localised to decidual cells and CD68+macrophages in 1(st) trimester decidua. This study demonstrated that EVT secretions, including PFN1, enhanced HESC decidualization and motility. This study has identified a new pathway that facilitates appropriate decidualization during the establishment of pregnancy. Nature Publishing Group UK 2017-08-18 /pmc/articles/PMC5562808/ /pubmed/28821715 http://dx.doi.org/10.1038/s41598-017-05947-0 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Menkhorst, E. M.
Van Sinderen, M. L.
Rainczuk, K.
Cuman, C.
Winship, A.
Dimitriadis, E.
Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5
title Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5
title_full Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5
title_fullStr Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5
title_full_unstemmed Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5
title_short Invasive trophoblast promote stromal fibroblast decidualization via Profilin 1 and ALOX5
title_sort invasive trophoblast promote stromal fibroblast decidualization via profilin 1 and alox5
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562808/
https://www.ncbi.nlm.nih.gov/pubmed/28821715
http://dx.doi.org/10.1038/s41598-017-05947-0
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