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Follicle development as an orchestrated signaling network in a 3D organoid
The ovarian follicle is the structural and functional unit of the ovary, composed of the female gamete (the oocyte) and supportive somatic cells. Follicles are not only the source of a female’s germ cell supply, but also secrete important hormones necessary for proper endocrine function. Folliculoge...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327556/ https://www.ncbi.nlm.nih.gov/pubmed/30647770 http://dx.doi.org/10.1186/s13036-018-0134-3 |
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author | Jones, Andrea S. K. Shikanov, Ariella |
author_facet | Jones, Andrea S. K. Shikanov, Ariella |
author_sort | Jones, Andrea S. K. |
collection | PubMed |
description | The ovarian follicle is the structural and functional unit of the ovary, composed of the female gamete (the oocyte) and supportive somatic cells. Follicles are not only the source of a female’s germ cell supply, but also secrete important hormones necessary for proper endocrine function. Folliculogenesis, the growth and maturation of the follicular unit, is a complex process governed by both intrafollicular crosstalk and pituitary-secreted hormones. While the later stages of this process are gonadotropin-dependent, early folliculogenesis appears to be controlled by the ovarian microenvironment and intrafollicular paracrine and autocrine signaling. In vitro follicle culture remains challenging because of the limited knowledge of growth factors and other cytokines influencing early follicle growth. Here we discuss the current state of knowledge on paracrine and autocrine signaling influencing primary follicles as they develop into the antral stage. Given the importance of intrafollicular signaling and the ovarian microenvironment, we reviewed the current engineering approaches for in vitro follicle culture, including 3D systems using natural hydrogels such as alginate and synthetic hydrogels such as poly(ethylene glycol). Our discussion is focused on what drives the proliferation of granulosa cells, development of the thecal layer, and antrum formation—three processes integral to follicle growth up to the antral stage. Further research in this area may reveal the mechanisms behind these complex signaling relationships within the follicle, leading to more successful and physiologically-relevant in vitro culture methods that will translate well to clinical applications. |
format | Online Article Text |
id | pubmed-6327556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63275562019-01-15 Follicle development as an orchestrated signaling network in a 3D organoid Jones, Andrea S. K. Shikanov, Ariella J Biol Eng Review The ovarian follicle is the structural and functional unit of the ovary, composed of the female gamete (the oocyte) and supportive somatic cells. Follicles are not only the source of a female’s germ cell supply, but also secrete important hormones necessary for proper endocrine function. Folliculogenesis, the growth and maturation of the follicular unit, is a complex process governed by both intrafollicular crosstalk and pituitary-secreted hormones. While the later stages of this process are gonadotropin-dependent, early folliculogenesis appears to be controlled by the ovarian microenvironment and intrafollicular paracrine and autocrine signaling. In vitro follicle culture remains challenging because of the limited knowledge of growth factors and other cytokines influencing early follicle growth. Here we discuss the current state of knowledge on paracrine and autocrine signaling influencing primary follicles as they develop into the antral stage. Given the importance of intrafollicular signaling and the ovarian microenvironment, we reviewed the current engineering approaches for in vitro follicle culture, including 3D systems using natural hydrogels such as alginate and synthetic hydrogels such as poly(ethylene glycol). Our discussion is focused on what drives the proliferation of granulosa cells, development of the thecal layer, and antrum formation—three processes integral to follicle growth up to the antral stage. Further research in this area may reveal the mechanisms behind these complex signaling relationships within the follicle, leading to more successful and physiologically-relevant in vitro culture methods that will translate well to clinical applications. BioMed Central 2019-01-09 /pmc/articles/PMC6327556/ /pubmed/30647770 http://dx.doi.org/10.1186/s13036-018-0134-3 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Jones, Andrea S. K. Shikanov, Ariella Follicle development as an orchestrated signaling network in a 3D organoid |
title | Follicle development as an orchestrated signaling network in a 3D organoid |
title_full | Follicle development as an orchestrated signaling network in a 3D organoid |
title_fullStr | Follicle development as an orchestrated signaling network in a 3D organoid |
title_full_unstemmed | Follicle development as an orchestrated signaling network in a 3D organoid |
title_short | Follicle development as an orchestrated signaling network in a 3D organoid |
title_sort | follicle development as an orchestrated signaling network in a 3d organoid |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6327556/ https://www.ncbi.nlm.nih.gov/pubmed/30647770 http://dx.doi.org/10.1186/s13036-018-0134-3 |
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