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Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23
Accurate identification of abnormalities in the mouse embryo depends not only on comparisons with appropriate, developmental stage‐matched controls, but also on an appreciation of the range of anatomical variation that can be expected during normal development. Here we present a morphological, topol...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603791/ https://www.ncbi.nlm.nih.gov/pubmed/28776665 http://dx.doi.org/10.1111/joa.12663 |
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author | Geyer, Stefan H. Reissig, Lukas F. Hüsemann, Markus Höfle, Cordula Wilson, Robert Prin, Fabrice Szumska, Dorota Galli, Antonella Adams, David J. White, Jacqui Mohun, Timothy J. Weninger, Wolfgang J. |
author_facet | Geyer, Stefan H. Reissig, Lukas F. Hüsemann, Markus Höfle, Cordula Wilson, Robert Prin, Fabrice Szumska, Dorota Galli, Antonella Adams, David J. White, Jacqui Mohun, Timothy J. Weninger, Wolfgang J. |
author_sort | Geyer, Stefan H. |
collection | PubMed |
description | Accurate identification of abnormalities in the mouse embryo depends not only on comparisons with appropriate, developmental stage‐matched controls, but also on an appreciation of the range of anatomical variation that can be expected during normal development. Here we present a morphological, topological and metric analysis of the heart and arteries of mouse embryos harvested on embryonic day (E)14.5, based on digital volume data of whole embryos analysed by high‐resolution episcopic microscopy (HREM). By comparing data from 206 genetically normal embryos, we have analysed the range and frequency of normal anatomical variations in the heart and major arteries across Theiler stages S21–S23. Using this, we have identified abnormalities in these structures among 298 embryos from mutant mouse lines carrying embryonic lethal gene mutations produced for the Deciphering the Mechanisms of Developmental Disorders (DMDD) programme. We present examples of both commonly occurring abnormal phenotypes and novel pathologies that most likely alter haemodynamics in these genetically altered mouse embryos. Our findings offer a reference baseline for identifying accurately abnormalities of the heart and arteries in embryos that have largely completed organogenesis. |
format | Online Article Text |
id | pubmed-5603791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56037912017-09-20 Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 Geyer, Stefan H. Reissig, Lukas F. Hüsemann, Markus Höfle, Cordula Wilson, Robert Prin, Fabrice Szumska, Dorota Galli, Antonella Adams, David J. White, Jacqui Mohun, Timothy J. Weninger, Wolfgang J. J Anat Original Articles Accurate identification of abnormalities in the mouse embryo depends not only on comparisons with appropriate, developmental stage‐matched controls, but also on an appreciation of the range of anatomical variation that can be expected during normal development. Here we present a morphological, topological and metric analysis of the heart and arteries of mouse embryos harvested on embryonic day (E)14.5, based on digital volume data of whole embryos analysed by high‐resolution episcopic microscopy (HREM). By comparing data from 206 genetically normal embryos, we have analysed the range and frequency of normal anatomical variations in the heart and major arteries across Theiler stages S21–S23. Using this, we have identified abnormalities in these structures among 298 embryos from mutant mouse lines carrying embryonic lethal gene mutations produced for the Deciphering the Mechanisms of Developmental Disorders (DMDD) programme. We present examples of both commonly occurring abnormal phenotypes and novel pathologies that most likely alter haemodynamics in these genetically altered mouse embryos. Our findings offer a reference baseline for identifying accurately abnormalities of the heart and arteries in embryos that have largely completed organogenesis. John Wiley and Sons Inc. 2017-08-03 2017-10 /pmc/articles/PMC5603791/ /pubmed/28776665 http://dx.doi.org/10.1111/joa.12663 Text en © 2017 The Authors. Journal of Anatomy published by John Wiley & Sons Ltd on behalf of Anatomical Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Geyer, Stefan H. Reissig, Lukas F. Hüsemann, Markus Höfle, Cordula Wilson, Robert Prin, Fabrice Szumska, Dorota Galli, Antonella Adams, David J. White, Jacqui Mohun, Timothy J. Weninger, Wolfgang J. Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 |
title | Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 |
title_full | Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 |
title_fullStr | Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 |
title_full_unstemmed | Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 |
title_short | Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23 |
title_sort | morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages s21–s23 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603791/ https://www.ncbi.nlm.nih.gov/pubmed/28776665 http://dx.doi.org/10.1111/joa.12663 |
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