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Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’
BACKGROUND: Functional male gametes are produced through complex processes that take place within the testis, epididymis and female reproductive tract. A breakdown at any of these phases can result in male infertility. The production of mutant mouse models often yields an unexpected male infertility...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816191/ https://www.ncbi.nlm.nih.gov/pubmed/19758979 http://dx.doi.org/10.1093/humupd/dmp032 |
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author | Borg, Claire L. Wolski, Katja M. Gibbs, Gerard M. O'Bryan, Moira K. |
author_facet | Borg, Claire L. Wolski, Katja M. Gibbs, Gerard M. O'Bryan, Moira K. |
author_sort | Borg, Claire L. |
collection | PubMed |
description | BACKGROUND: Functional male gametes are produced through complex processes that take place within the testis, epididymis and female reproductive tract. A breakdown at any of these phases can result in male infertility. The production of mutant mouse models often yields an unexpected male infertility phenotype. It is with this in mind that the current review has been written. The review aims to act as a guide to the ‘non-reproductive biologist’ to facilitate a systematic analysis of sterile or subfertile mice and to assist in extracting the maximum amount of information from each model. METHODS: This is a review of the original literature on defects in the processes that take a mouse spermatogonial stem cell through to a fully functional spermatozoon, which result in male infertility. Based on literature searches and personal experience, we have outlined a step-by-step strategy for the analysis of an infertile male mouse line. RESULTS: A wide range of methods can be used to define the phenotype of an infertile male mouse. These methods range from histological methods such as electron microscopy and immunohistochemistry, to hormone analyses and methods to assess sperm maturation status and functional competence. CONCLUSION: With the increased rate of genetically modified mouse production, the generation of mouse models with unexpected male infertility is increasing. This manuscript will help to ensure that the maximum amount of information is obtained from each mouse model and, by extension, will facilitate the knowledge of both normal fertility processes and the causes of human infertility. |
format | Text |
id | pubmed-2816191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28161912010-02-04 Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ Borg, Claire L. Wolski, Katja M. Gibbs, Gerard M. O'Bryan, Moira K. Hum Reprod Update Reviews BACKGROUND: Functional male gametes are produced through complex processes that take place within the testis, epididymis and female reproductive tract. A breakdown at any of these phases can result in male infertility. The production of mutant mouse models often yields an unexpected male infertility phenotype. It is with this in mind that the current review has been written. The review aims to act as a guide to the ‘non-reproductive biologist’ to facilitate a systematic analysis of sterile or subfertile mice and to assist in extracting the maximum amount of information from each model. METHODS: This is a review of the original literature on defects in the processes that take a mouse spermatogonial stem cell through to a fully functional spermatozoon, which result in male infertility. Based on literature searches and personal experience, we have outlined a step-by-step strategy for the analysis of an infertile male mouse line. RESULTS: A wide range of methods can be used to define the phenotype of an infertile male mouse. These methods range from histological methods such as electron microscopy and immunohistochemistry, to hormone analyses and methods to assess sperm maturation status and functional competence. CONCLUSION: With the increased rate of genetically modified mouse production, the generation of mouse models with unexpected male infertility is increasing. This manuscript will help to ensure that the maximum amount of information is obtained from each mouse model and, by extension, will facilitate the knowledge of both normal fertility processes and the causes of human infertility. Oxford University Press 2010 2009-09-15 /pmc/articles/PMC2816191/ /pubmed/19758979 http://dx.doi.org/10.1093/humupd/dmp032 Text en © The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Borg, Claire L. Wolski, Katja M. Gibbs, Gerard M. O'Bryan, Moira K. Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
title | Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
title_full | Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
title_fullStr | Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
title_full_unstemmed | Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
title_short | Phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
title_sort | phenotyping male infertility in the mouse: how to get the most out of a ‘non-performer’ |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816191/ https://www.ncbi.nlm.nih.gov/pubmed/19758979 http://dx.doi.org/10.1093/humupd/dmp032 |
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