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Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary

In the mouse ovary, folliculogenesis proceeds through eight main growth stages, from small primordial type 1 (T1) to fully grown antral T8 follicles. Most of our understanding of this process was obtained with approaches that disrupted the ovary three-dimensional (3D) integrity. Micro-Computed Tomog...

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Autores principales: Fiorentino, Giulia, Parrilli, Annapaola, Garagna, Silvia, Zuccotti, Maurizio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7604317/
https://www.ncbi.nlm.nih.gov/pubmed/33195196
http://dx.doi.org/10.3389/fcell.2020.566152
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author Fiorentino, Giulia
Parrilli, Annapaola
Garagna, Silvia
Zuccotti, Maurizio
author_facet Fiorentino, Giulia
Parrilli, Annapaola
Garagna, Silvia
Zuccotti, Maurizio
author_sort Fiorentino, Giulia
collection PubMed
description In the mouse ovary, folliculogenesis proceeds through eight main growth stages, from small primordial type 1 (T1) to fully grown antral T8 follicles. Most of our understanding of this process was obtained with approaches that disrupted the ovary three-dimensional (3D) integrity. Micro-Computed Tomography (microCT) allows the maintenance of the organ structure and a true in-silico 3D reconstruction, with cubic voxels and isotropic resolution, giving a precise spatial mapping of its functional units. Here, we developed a robust method that, by combining an optimized contrast procedure with microCT imaging of the tiny adult mouse ovary, allowed 3D mapping and counting of follicles, from pre-antral secondary T4 (53.2 ± 12.7 μm in diameter) to antral T8 (321.0 ± 21.3 μm) and corpora lutea, together with the major vasculature branches. Primordial and primary follicles (T1–T3) could not be observed. Our procedure highlighted, with unprecedent details, the main functional compartments of the growing follicle: granulosa, antrum, cumulus cells, zona pellucida, and oocyte with its nucleus. The results describe a homogeneous distribution of all follicle types between the ovary dorsal and ventral regions. Also, they show that each of the eight sectors, virtually segmented along the dorsal-ventral axis, houses an equal number of each follicle type. Altogether, these data suggest that follicle recruitment is homogeneously distributed all-over the ovarian surface. This topographic reconstruction builds sound bases for modeling follicles position and, prospectively, could contribute to our understanding of folliculogenesis dynamics, not only under normal conditions, but, importantly, during aging, in the presence of pathologies or after hormones or drugs administration.
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spelling pubmed-76043172020-11-13 Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary Fiorentino, Giulia Parrilli, Annapaola Garagna, Silvia Zuccotti, Maurizio Front Cell Dev Biol Cell and Developmental Biology In the mouse ovary, folliculogenesis proceeds through eight main growth stages, from small primordial type 1 (T1) to fully grown antral T8 follicles. Most of our understanding of this process was obtained with approaches that disrupted the ovary three-dimensional (3D) integrity. Micro-Computed Tomography (microCT) allows the maintenance of the organ structure and a true in-silico 3D reconstruction, with cubic voxels and isotropic resolution, giving a precise spatial mapping of its functional units. Here, we developed a robust method that, by combining an optimized contrast procedure with microCT imaging of the tiny adult mouse ovary, allowed 3D mapping and counting of follicles, from pre-antral secondary T4 (53.2 ± 12.7 μm in diameter) to antral T8 (321.0 ± 21.3 μm) and corpora lutea, together with the major vasculature branches. Primordial and primary follicles (T1–T3) could not be observed. Our procedure highlighted, with unprecedent details, the main functional compartments of the growing follicle: granulosa, antrum, cumulus cells, zona pellucida, and oocyte with its nucleus. The results describe a homogeneous distribution of all follicle types between the ovary dorsal and ventral regions. Also, they show that each of the eight sectors, virtually segmented along the dorsal-ventral axis, houses an equal number of each follicle type. Altogether, these data suggest that follicle recruitment is homogeneously distributed all-over the ovarian surface. This topographic reconstruction builds sound bases for modeling follicles position and, prospectively, could contribute to our understanding of folliculogenesis dynamics, not only under normal conditions, but, importantly, during aging, in the presence of pathologies or after hormones or drugs administration. Frontiers Media S.A. 2020-10-19 /pmc/articles/PMC7604317/ /pubmed/33195196 http://dx.doi.org/10.3389/fcell.2020.566152 Text en Copyright © 2020 Fiorentino, Parrilli, Garagna and Zuccotti. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Fiorentino, Giulia
Parrilli, Annapaola
Garagna, Silvia
Zuccotti, Maurizio
Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary
title Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary
title_full Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary
title_fullStr Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary
title_full_unstemmed Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary
title_short Three-Dimensional Micro-Computed Tomography of the Adult Mouse Ovary
title_sort three-dimensional micro-computed tomography of the adult mouse ovary
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7604317/
https://www.ncbi.nlm.nih.gov/pubmed/33195196
http://dx.doi.org/10.3389/fcell.2020.566152
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