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Models of in vitro spermatogenesis

Understanding the mechanisms that lead to the differentiation of male germ cells from their spermatogonial stem cells through meiosis to give rise to mature haploid spermatozoa has been a major quest for many decades. Unlike most other cell types this differentiation process is more or less complete...

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Detalles Bibliográficos
Autores principales: Hunter, Damien, Anand-Ivell, Ravinder, Danner, Sandra, Ivell, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341244/
https://www.ncbi.nlm.nih.gov/pubmed/22553488
http://dx.doi.org/10.4161/spmg.19383
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author Hunter, Damien
Anand-Ivell, Ravinder
Danner, Sandra
Ivell, Richard
author_facet Hunter, Damien
Anand-Ivell, Ravinder
Danner, Sandra
Ivell, Richard
author_sort Hunter, Damien
collection PubMed
description Understanding the mechanisms that lead to the differentiation of male germ cells from their spermatogonial stem cells through meiosis to give rise to mature haploid spermatozoa has been a major quest for many decades. Unlike most other cell types this differentiation process is more or less completely dependent upon the cells being located within the strongly structured niche provided by mature Sertoli cells within an intact seminiferous epithelium. While much new information is currently being obtained through the application and description of relevant gene mutations, there is still a considerable need for in vitro models with which to explore the mechanisms involved. Not only are systems of in vitro spermatogenesis important for understanding the basic science, they have marked pragmatic value in offering ex vivo systems for the artificial maturation of immature germ cells from male infertility patients, as well as providing opportunities for the transgenic manipulation of male germ cells. In this review, we have summarized literature relating to simplistic culturing of germ cells, co-cultures of germ cells with other cell types, especially with Sertoli cells, cultures of seminiferous tubule fragments, and briefly mention the opportunities of xenografting larger testicular pieces. The majority of methods are successful in allowing the differentiation of small steps in the progress of spermatogonia to spermatozoa; few tolerate the chromosomal reduction division through meiosis, and even fewer seem able to complete the complex morphogenesis which results in freely swimming spermatozoa. However, recent progress with complex culture environments, such as 3-d matrices, suggest that possibly success is now not too far away.
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spelling pubmed-33412442012-05-02 Models of in vitro spermatogenesis Hunter, Damien Anand-Ivell, Ravinder Danner, Sandra Ivell, Richard Spermatogenesis Review Understanding the mechanisms that lead to the differentiation of male germ cells from their spermatogonial stem cells through meiosis to give rise to mature haploid spermatozoa has been a major quest for many decades. Unlike most other cell types this differentiation process is more or less completely dependent upon the cells being located within the strongly structured niche provided by mature Sertoli cells within an intact seminiferous epithelium. While much new information is currently being obtained through the application and description of relevant gene mutations, there is still a considerable need for in vitro models with which to explore the mechanisms involved. Not only are systems of in vitro spermatogenesis important for understanding the basic science, they have marked pragmatic value in offering ex vivo systems for the artificial maturation of immature germ cells from male infertility patients, as well as providing opportunities for the transgenic manipulation of male germ cells. In this review, we have summarized literature relating to simplistic culturing of germ cells, co-cultures of germ cells with other cell types, especially with Sertoli cells, cultures of seminiferous tubule fragments, and briefly mention the opportunities of xenografting larger testicular pieces. The majority of methods are successful in allowing the differentiation of small steps in the progress of spermatogonia to spermatozoa; few tolerate the chromosomal reduction division through meiosis, and even fewer seem able to complete the complex morphogenesis which results in freely swimming spermatozoa. However, recent progress with complex culture environments, such as 3-d matrices, suggest that possibly success is now not too far away. Landes Bioscience 2012-01-01 /pmc/articles/PMC3341244/ /pubmed/22553488 http://dx.doi.org/10.4161/spmg.19383 Text en Copyright © 2012 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Hunter, Damien
Anand-Ivell, Ravinder
Danner, Sandra
Ivell, Richard
Models of in vitro spermatogenesis
title Models of in vitro spermatogenesis
title_full Models of in vitro spermatogenesis
title_fullStr Models of in vitro spermatogenesis
title_full_unstemmed Models of in vitro spermatogenesis
title_short Models of in vitro spermatogenesis
title_sort models of in vitro spermatogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341244/
https://www.ncbi.nlm.nih.gov/pubmed/22553488
http://dx.doi.org/10.4161/spmg.19383
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