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Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry
Spermatogenesis is a highly ordered developmental program that produces haploid male germ cells. The study of male germ cell development in the mouse has provided unique perspectives into the molecular mechanisms that control cell development and differentiation in mammals, including tissue‐specific...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519249/ https://www.ncbi.nlm.nih.gov/pubmed/30663216 http://dx.doi.org/10.1002/dvg.23283 |
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author | Zagore, Leah L. Akesson, Cydni C. Licatalosi, Donny D. |
author_facet | Zagore, Leah L. Akesson, Cydni C. Licatalosi, Donny D. |
author_sort | Zagore, Leah L. |
collection | PubMed |
description | Spermatogenesis is a highly ordered developmental program that produces haploid male germ cells. The study of male germ cell development in the mouse has provided unique perspectives into the molecular mechanisms that control cell development and differentiation in mammals, including tissue‐specific gene regulatory programs. An intrinsic challenge in spermatogenesis research is the heterogeneity of germ and somatic cell types present in the testis. Techniques to separate and isolate distinct mouse spermatogenic cell types have great potential to shed light on molecular mechanisms controlling mammalian cell development, while also providing new insights into cellular events important for human reproductive health. Here, we detail a versatile strategy that combines Cre‐lox technology to fluorescently label germ cells, with flow cytometry to discriminate and isolate germ cells in different stages of development for cellular and molecular analyses. |
format | Online Article Text |
id | pubmed-6519249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65192492019-08-29 Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry Zagore, Leah L. Akesson, Cydni C. Licatalosi, Donny D. Genesis Technology Report Spermatogenesis is a highly ordered developmental program that produces haploid male germ cells. The study of male germ cell development in the mouse has provided unique perspectives into the molecular mechanisms that control cell development and differentiation in mammals, including tissue‐specific gene regulatory programs. An intrinsic challenge in spermatogenesis research is the heterogeneity of germ and somatic cell types present in the testis. Techniques to separate and isolate distinct mouse spermatogenic cell types have great potential to shed light on molecular mechanisms controlling mammalian cell development, while also providing new insights into cellular events important for human reproductive health. Here, we detail a versatile strategy that combines Cre‐lox technology to fluorescently label germ cells, with flow cytometry to discriminate and isolate germ cells in different stages of development for cellular and molecular analyses. John Wiley and Sons Inc. 2019-02-06 2019-04 /pmc/articles/PMC6519249/ /pubmed/30663216 http://dx.doi.org/10.1002/dvg.23283 Text en © 2019 The Authors. Genesis published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Technology Report Zagore, Leah L. Akesson, Cydni C. Licatalosi, Donny D. Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry |
title | Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry |
title_full | Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry |
title_fullStr | Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry |
title_full_unstemmed | Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry |
title_short | Efficient GFP‐labeling and analysis of spermatogenic cells using the IRG transgene and flow cytometry |
title_sort | efficient gfp‐labeling and analysis of spermatogenic cells using the irg transgene and flow cytometry |
topic | Technology Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6519249/ https://www.ncbi.nlm.nih.gov/pubmed/30663216 http://dx.doi.org/10.1002/dvg.23283 |
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