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A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance
In eutherians, the placenta acts as a barrier and conduit at the maternal-fetal interface. Syncytiotrophoblasts, the multinucleated cells that cover the placental villous tree surfaces of the human placenta, are directly bathed in maternal blood and are formed by the fusion of progenitor cytotrophob...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783126/ https://www.ncbi.nlm.nih.gov/pubmed/26973875 http://dx.doi.org/10.1126/sciadv.1501462 |
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author | McConkey, Cameron A. Delorme-Axford, Elizabeth Nickerson, Cheryl A. Kim, Kwang Sik Sadovsky, Yoel Boyle, Jon P. Coyne, Carolyn B. |
author_facet | McConkey, Cameron A. Delorme-Axford, Elizabeth Nickerson, Cheryl A. Kim, Kwang Sik Sadovsky, Yoel Boyle, Jon P. Coyne, Carolyn B. |
author_sort | McConkey, Cameron A. |
collection | PubMed |
description | In eutherians, the placenta acts as a barrier and conduit at the maternal-fetal interface. Syncytiotrophoblasts, the multinucleated cells that cover the placental villous tree surfaces of the human placenta, are directly bathed in maternal blood and are formed by the fusion of progenitor cytotrophoblasts that underlie them. Despite their crucial role in fetal protection, many of the events that govern trophoblast fusion and protection from microbial infection are unknown. We describe a three-dimensional (3D)–based culture model using human JEG-3 trophoblast cells that develop syncytiotrophoblast phenotypes when cocultured with human microvascular endothelial cells. JEG-3 cells cultured in this system exhibit enhanced fusogenic activity and morphological and secretory activities strikingly similar to those of primary human syncytiotrophoblasts. RNASeq analyses extend the observed functional similarities to the transcriptome, where we observed significant overlap between syncytiotrophoblast-specific genes and 3D JEG-3 cultures. Furthermore, JEG-3 cells cultured in 3D are resistant to infection by viruses and Toxoplasma gondii, which mimics the high resistance of syncytiotrophoblasts to microbial infections in vivo. Given that this system is genetically manipulatable, it provides a new platform to dissect the mechanisms involved in syncytiotrophoblast development and microbial resistance. |
format | Online Article Text |
id | pubmed-4783126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47831262016-03-11 A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance McConkey, Cameron A. Delorme-Axford, Elizabeth Nickerson, Cheryl A. Kim, Kwang Sik Sadovsky, Yoel Boyle, Jon P. Coyne, Carolyn B. Sci Adv Research Articles In eutherians, the placenta acts as a barrier and conduit at the maternal-fetal interface. Syncytiotrophoblasts, the multinucleated cells that cover the placental villous tree surfaces of the human placenta, are directly bathed in maternal blood and are formed by the fusion of progenitor cytotrophoblasts that underlie them. Despite their crucial role in fetal protection, many of the events that govern trophoblast fusion and protection from microbial infection are unknown. We describe a three-dimensional (3D)–based culture model using human JEG-3 trophoblast cells that develop syncytiotrophoblast phenotypes when cocultured with human microvascular endothelial cells. JEG-3 cells cultured in this system exhibit enhanced fusogenic activity and morphological and secretory activities strikingly similar to those of primary human syncytiotrophoblasts. RNASeq analyses extend the observed functional similarities to the transcriptome, where we observed significant overlap between syncytiotrophoblast-specific genes and 3D JEG-3 cultures. Furthermore, JEG-3 cells cultured in 3D are resistant to infection by viruses and Toxoplasma gondii, which mimics the high resistance of syncytiotrophoblasts to microbial infections in vivo. Given that this system is genetically manipulatable, it provides a new platform to dissect the mechanisms involved in syncytiotrophoblast development and microbial resistance. American Association for the Advancement of Science 2016-03-04 /pmc/articles/PMC4783126/ /pubmed/26973875 http://dx.doi.org/10.1126/sciadv.1501462 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles McConkey, Cameron A. Delorme-Axford, Elizabeth Nickerson, Cheryl A. Kim, Kwang Sik Sadovsky, Yoel Boyle, Jon P. Coyne, Carolyn B. A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
title | A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
title_full | A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
title_fullStr | A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
title_full_unstemmed | A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
title_short | A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
title_sort | three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4783126/ https://www.ncbi.nlm.nih.gov/pubmed/26973875 http://dx.doi.org/10.1126/sciadv.1501462 |
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