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Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta

Trophoblast stem (TS) cells in the mouse derive from the polar trophectoderm of the blastocyst and persist through early gestation (to E8.5) to support placental development. Further development and growth is proposed to rely on layer-restricted progenitor cells. Stem cell antigen (Sca) -1 is a memb...

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Autores principales: Natale, Bryony V., Schweitzer, Christina, Hughes, Martha, Globisch, Maria A., Kotadia, Ramie, Tremblay, Emilie, Vu, Priscilla, Cross, James C., Natale, David R. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514127/
https://www.ncbi.nlm.nih.gov/pubmed/28717241
http://dx.doi.org/10.1038/s41598-017-06008-2
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author Natale, Bryony V.
Schweitzer, Christina
Hughes, Martha
Globisch, Maria A.
Kotadia, Ramie
Tremblay, Emilie
Vu, Priscilla
Cross, James C.
Natale, David R. C.
author_facet Natale, Bryony V.
Schweitzer, Christina
Hughes, Martha
Globisch, Maria A.
Kotadia, Ramie
Tremblay, Emilie
Vu, Priscilla
Cross, James C.
Natale, David R. C.
author_sort Natale, Bryony V.
collection PubMed
description Trophoblast stem (TS) cells in the mouse derive from the polar trophectoderm of the blastocyst and persist through early gestation (to E8.5) to support placental development. Further development and growth is proposed to rely on layer-restricted progenitor cells. Stem cell antigen (Sca) -1 is a member of the Ly6 gene family and a known marker of stem cells in both hematopoietic and non-hematopoietic mouse tissues. Having identified that Sca-1 mRNA was highly expressed in mouse TS cells in culture, we found that it was also expressed in a subset of trophoblast within the chorion and labyrinth layer of the mouse placenta. Isolation and in vitro culture of Sca-1(+) trophoblast cells from both differentiated TS cell cultures and dissected mouse placentae resulted in proliferating colonies that expressed known markers of TS cells. Furthermore, these cells could be stimulated to differentiate and expressed markers of both junctional zone and labyrinth trophoblast subtypes in a manner comparable to established mouse TS cell lines. Our results suggest that we have identified a subpopulation of TS cell-like cells that persist in the mid- to late- gestation mouse placenta as well as a cell surface protein that can be used to identify and isolate these cells.
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spelling pubmed-55141272017-07-19 Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta Natale, Bryony V. Schweitzer, Christina Hughes, Martha Globisch, Maria A. Kotadia, Ramie Tremblay, Emilie Vu, Priscilla Cross, James C. Natale, David R. C. Sci Rep Article Trophoblast stem (TS) cells in the mouse derive from the polar trophectoderm of the blastocyst and persist through early gestation (to E8.5) to support placental development. Further development and growth is proposed to rely on layer-restricted progenitor cells. Stem cell antigen (Sca) -1 is a member of the Ly6 gene family and a known marker of stem cells in both hematopoietic and non-hematopoietic mouse tissues. Having identified that Sca-1 mRNA was highly expressed in mouse TS cells in culture, we found that it was also expressed in a subset of trophoblast within the chorion and labyrinth layer of the mouse placenta. Isolation and in vitro culture of Sca-1(+) trophoblast cells from both differentiated TS cell cultures and dissected mouse placentae resulted in proliferating colonies that expressed known markers of TS cells. Furthermore, these cells could be stimulated to differentiate and expressed markers of both junctional zone and labyrinth trophoblast subtypes in a manner comparable to established mouse TS cell lines. Our results suggest that we have identified a subpopulation of TS cell-like cells that persist in the mid- to late- gestation mouse placenta as well as a cell surface protein that can be used to identify and isolate these cells. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514127/ /pubmed/28717241 http://dx.doi.org/10.1038/s41598-017-06008-2 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
Natale, Bryony V.
Schweitzer, Christina
Hughes, Martha
Globisch, Maria A.
Kotadia, Ramie
Tremblay, Emilie
Vu, Priscilla
Cross, James C.
Natale, David R. C.
Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
title Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
title_full Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
title_fullStr Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
title_full_unstemmed Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
title_short Sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
title_sort sca-1 identifies a trophoblast population with multipotent potential in the mid-gestation mouse placenta
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514127/
https://www.ncbi.nlm.nih.gov/pubmed/28717241
http://dx.doi.org/10.1038/s41598-017-06008-2
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