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The mammalian decidual cell evolved from a cellular stress response
Among animal species, cell types vary greatly in terms of number and kind. The number of cell types found within an organism differs considerably between species, and cell type diversity is a significant contributor to differences in organismal structure and function. These observations suggest that...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108454/ https://www.ncbi.nlm.nih.gov/pubmed/30142145 http://dx.doi.org/10.1371/journal.pbio.2005594 |
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author | Erkenbrack, Eric M. Maziarz, Jamie D. Griffith, Oliver W. Liang, Cong Chavan, Arun R. Nnamani, Mauris C. Wagner, Günter P. |
author_facet | Erkenbrack, Eric M. Maziarz, Jamie D. Griffith, Oliver W. Liang, Cong Chavan, Arun R. Nnamani, Mauris C. Wagner, Günter P. |
author_sort | Erkenbrack, Eric M. |
collection | PubMed |
description | Among animal species, cell types vary greatly in terms of number and kind. The number of cell types found within an organism differs considerably between species, and cell type diversity is a significant contributor to differences in organismal structure and function. These observations suggest that cell type origination is a significant source of evolutionary novelty. The molecular mechanisms that result in the evolution of novel cell types, however, are poorly understood. Here, we show that a novel cell type of eutherians mammals, the decidual stromal cell (DSC), evolved by rewiring an ancestral cellular stress response. We isolated the precursor cell type of DSCs, endometrial stromal fibroblasts (ESFs), from the opossum Monodelphis domestica. We show that, in opossum ESFs, the majority of decidual core regulatory genes respond to decidualizing signals but do not regulate decidual effector genes. Rather, in opossum ESFs, decidual transcription factors function in apoptotic and oxidative stress response. We propose that rewiring of cellular stress responses was an important mechanism for the evolution of the eutherian decidual cell type. |
format | Online Article Text |
id | pubmed-6108454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61084542018-09-18 The mammalian decidual cell evolved from a cellular stress response Erkenbrack, Eric M. Maziarz, Jamie D. Griffith, Oliver W. Liang, Cong Chavan, Arun R. Nnamani, Mauris C. Wagner, Günter P. PLoS Biol Research Article Among animal species, cell types vary greatly in terms of number and kind. The number of cell types found within an organism differs considerably between species, and cell type diversity is a significant contributor to differences in organismal structure and function. These observations suggest that cell type origination is a significant source of evolutionary novelty. The molecular mechanisms that result in the evolution of novel cell types, however, are poorly understood. Here, we show that a novel cell type of eutherians mammals, the decidual stromal cell (DSC), evolved by rewiring an ancestral cellular stress response. We isolated the precursor cell type of DSCs, endometrial stromal fibroblasts (ESFs), from the opossum Monodelphis domestica. We show that, in opossum ESFs, the majority of decidual core regulatory genes respond to decidualizing signals but do not regulate decidual effector genes. Rather, in opossum ESFs, decidual transcription factors function in apoptotic and oxidative stress response. We propose that rewiring of cellular stress responses was an important mechanism for the evolution of the eutherian decidual cell type. Public Library of Science 2018-08-24 /pmc/articles/PMC6108454/ /pubmed/30142145 http://dx.doi.org/10.1371/journal.pbio.2005594 Text en © 2018 Erkenbrack et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Erkenbrack, Eric M. Maziarz, Jamie D. Griffith, Oliver W. Liang, Cong Chavan, Arun R. Nnamani, Mauris C. Wagner, Günter P. The mammalian decidual cell evolved from a cellular stress response |
title | The mammalian decidual cell evolved from a cellular stress response |
title_full | The mammalian decidual cell evolved from a cellular stress response |
title_fullStr | The mammalian decidual cell evolved from a cellular stress response |
title_full_unstemmed | The mammalian decidual cell evolved from a cellular stress response |
title_short | The mammalian decidual cell evolved from a cellular stress response |
title_sort | mammalian decidual cell evolved from a cellular stress response |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108454/ https://www.ncbi.nlm.nih.gov/pubmed/30142145 http://dx.doi.org/10.1371/journal.pbio.2005594 |
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