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Murine transcription factor Math6 is a regulator of placenta development
The murine basic helix-loop-helix transcription (bHLH) factor mouse atonal homolog 6 (Math6) is expressed in numerous organs and supposed to be involved in several developmental processes. However, so far neither all aspects nor the molecular mechanisms of Math6 function have been explored exhaustiv...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177472/ https://www.ncbi.nlm.nih.gov/pubmed/30301918 http://dx.doi.org/10.1038/s41598-018-33387-x |
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author | Böing, Marion Brand-Saberi, Beate Napirei, Markus |
author_facet | Böing, Marion Brand-Saberi, Beate Napirei, Markus |
author_sort | Böing, Marion |
collection | PubMed |
description | The murine basic helix-loop-helix transcription (bHLH) factor mouse atonal homolog 6 (Math6) is expressed in numerous organs and supposed to be involved in several developmental processes. However, so far neither all aspects nor the molecular mechanisms of Math6 function have been explored exhaustively. To analyze the in vivo function of Math6 in detail, we generated a constitutive knockout (KO) mouse (Math6(−/−)) and performed an initial histological and molecular biological investigation of its main phenotype. Pregnant Math6(−/−) females suffer from a disturbed early placental development leading to the death of the majority of embryos independent of the embryonic Math6 genotype. A few placentas and fetuses survive the severe uterine hemorrhagic events at late mid-gestation (E13.5) and subsequently develop regularly. However, these fetuses could not be born due to obstructions within the gravid uterus, which hinder the birth process. Characterization of the endogenous spatiotemporal Math6 expression during placenta development reveals that Math6 is essential for an ordered decidualization and an important regulator of the maternal-fetal endocrine crosstalk regulating endometrial trophoblast invasion and differentiation. The strongly disturbed vascularization observed in the maternal placenta appears as an additional consequence of the altered endocrine status and as the main cause for the general hemorrhagic crisis. |
format | Online Article Text |
id | pubmed-6177472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61774722018-10-12 Murine transcription factor Math6 is a regulator of placenta development Böing, Marion Brand-Saberi, Beate Napirei, Markus Sci Rep Article The murine basic helix-loop-helix transcription (bHLH) factor mouse atonal homolog 6 (Math6) is expressed in numerous organs and supposed to be involved in several developmental processes. However, so far neither all aspects nor the molecular mechanisms of Math6 function have been explored exhaustively. To analyze the in vivo function of Math6 in detail, we generated a constitutive knockout (KO) mouse (Math6(−/−)) and performed an initial histological and molecular biological investigation of its main phenotype. Pregnant Math6(−/−) females suffer from a disturbed early placental development leading to the death of the majority of embryos independent of the embryonic Math6 genotype. A few placentas and fetuses survive the severe uterine hemorrhagic events at late mid-gestation (E13.5) and subsequently develop regularly. However, these fetuses could not be born due to obstructions within the gravid uterus, which hinder the birth process. Characterization of the endogenous spatiotemporal Math6 expression during placenta development reveals that Math6 is essential for an ordered decidualization and an important regulator of the maternal-fetal endocrine crosstalk regulating endometrial trophoblast invasion and differentiation. The strongly disturbed vascularization observed in the maternal placenta appears as an additional consequence of the altered endocrine status and as the main cause for the general hemorrhagic crisis. Nature Publishing Group UK 2018-10-09 /pmc/articles/PMC6177472/ /pubmed/30301918 http://dx.doi.org/10.1038/s41598-018-33387-x Text en © The Author(s) 2018 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 Böing, Marion Brand-Saberi, Beate Napirei, Markus Murine transcription factor Math6 is a regulator of placenta development |
title | Murine transcription factor Math6 is a regulator of placenta development |
title_full | Murine transcription factor Math6 is a regulator of placenta development |
title_fullStr | Murine transcription factor Math6 is a regulator of placenta development |
title_full_unstemmed | Murine transcription factor Math6 is a regulator of placenta development |
title_short | Murine transcription factor Math6 is a regulator of placenta development |
title_sort | murine transcription factor math6 is a regulator of placenta development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177472/ https://www.ncbi.nlm.nih.gov/pubmed/30301918 http://dx.doi.org/10.1038/s41598-018-33387-x |
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