Cargando…

Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes

The uterine luminal epithelium folds characteristically in mammals, including humans, horses and rodents. Improper uterine folding in horses results in pregnancy failure, but the precise function of folds remains unknown. Here, we uncover dynamic changes in the 3D uterine folding pattern during earl...

Descripción completa

Detalles Bibliográficos
Autores principales: Madhavan, Manoj K., DeMayo, Francesco J., Lydon, John P., Joshi, Niraj R., Fazleabas, Asgerally T., Arora, Ripla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245188/
https://www.ncbi.nlm.nih.gov/pubmed/35575097
http://dx.doi.org/10.1242/dev.200300
_version_ 1784738693966200832
author Madhavan, Manoj K.
DeMayo, Francesco J.
Lydon, John P.
Joshi, Niraj R.
Fazleabas, Asgerally T.
Arora, Ripla
author_facet Madhavan, Manoj K.
DeMayo, Francesco J.
Lydon, John P.
Joshi, Niraj R.
Fazleabas, Asgerally T.
Arora, Ripla
author_sort Madhavan, Manoj K.
collection PubMed
description The uterine luminal epithelium folds characteristically in mammals, including humans, horses and rodents. Improper uterine folding in horses results in pregnancy failure, but the precise function of folds remains unknown. Here, we uncover dynamic changes in the 3D uterine folding pattern during early pregnancy with the entire lumen forming pre-implantation transverse folds along the mesometrial-antimesometrial axis. Using a time course, we show that transverse folds are formed before embryo spacing, whereas implantation chambers form as the embryo begins attachment. Thus, folds and chambers are two distinct structures. Transverse folds resolve to form a flat implantation region, after which an embryo arrives at its center to attach and form the post-implantation chamber. Our data also suggest that the implantation chamber facilitates embryo rotation and its alignment along the uterine mesometrial-antimesometrial axis. Using WNT5A- and RBPJ-deficient mice that display aberrant folds, we show that embryos trapped in longitudinal folds display misalignment of the embryo-uterine axes, abnormal chamber formation and defective post-implantation morphogenesis. These mouse models with disrupted uterine folding provide an opportunity to understand uterine structure-based mechanisms that are crucial for implantation and pregnancy success. This article has an associated ‘The people behind the papers’ interview.
format Online
Article
Text
id pubmed-9245188
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-92451882022-07-07 Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes Madhavan, Manoj K. DeMayo, Francesco J. Lydon, John P. Joshi, Niraj R. Fazleabas, Asgerally T. Arora, Ripla Development Research Article The uterine luminal epithelium folds characteristically in mammals, including humans, horses and rodents. Improper uterine folding in horses results in pregnancy failure, but the precise function of folds remains unknown. Here, we uncover dynamic changes in the 3D uterine folding pattern during early pregnancy with the entire lumen forming pre-implantation transverse folds along the mesometrial-antimesometrial axis. Using a time course, we show that transverse folds are formed before embryo spacing, whereas implantation chambers form as the embryo begins attachment. Thus, folds and chambers are two distinct structures. Transverse folds resolve to form a flat implantation region, after which an embryo arrives at its center to attach and form the post-implantation chamber. Our data also suggest that the implantation chamber facilitates embryo rotation and its alignment along the uterine mesometrial-antimesometrial axis. Using WNT5A- and RBPJ-deficient mice that display aberrant folds, we show that embryos trapped in longitudinal folds display misalignment of the embryo-uterine axes, abnormal chamber formation and defective post-implantation morphogenesis. These mouse models with disrupted uterine folding provide an opportunity to understand uterine structure-based mechanisms that are crucial for implantation and pregnancy success. This article has an associated ‘The people behind the papers’ interview. The Company of Biologists Ltd 2022-06-13 /pmc/articles/PMC9245188/ /pubmed/35575097 http://dx.doi.org/10.1242/dev.200300 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Madhavan, Manoj K.
DeMayo, Francesco J.
Lydon, John P.
Joshi, Niraj R.
Fazleabas, Asgerally T.
Arora, Ripla
Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
title Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
title_full Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
title_fullStr Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
title_full_unstemmed Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
title_short Aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
title_sort aberrant uterine folding in mice disrupts implantation chamber formation and alignment of embryo-uterine axes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245188/
https://www.ncbi.nlm.nih.gov/pubmed/35575097
http://dx.doi.org/10.1242/dev.200300
work_keys_str_mv AT madhavanmanojk aberrantuterinefoldinginmicedisruptsimplantationchamberformationandalignmentofembryouterineaxes
AT demayofrancescoj aberrantuterinefoldinginmicedisruptsimplantationchamberformationandalignmentofembryouterineaxes
AT lydonjohnp aberrantuterinefoldinginmicedisruptsimplantationchamberformationandalignmentofembryouterineaxes
AT joshinirajr aberrantuterinefoldinginmicedisruptsimplantationchamberformationandalignmentofembryouterineaxes
AT fazleabasasgerallyt aberrantuterinefoldinginmicedisruptsimplantationchamberformationandalignmentofembryouterineaxes
AT aroraripla aberrantuterinefoldinginmicedisruptsimplantationchamberformationandalignmentofembryouterineaxes