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DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)

Spermatogonial stem cells (SSC) are essential for spermatogenesis and male fertility. In addition, these adult tissue stem cells can be used as vehicles for germline modification in animal models and may have application for treating male infertility. To facilitate the investigation of SSCs and germ...

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Autores principales: Gassei, Kathrin, Sheng, Yi, Fayomi, Adetunji, Mital, Payal, Sukhwani, Meena, Lin, Chih-Cheng, Peters, Karen A., Althouse, Andrew, Valli, Hanna, Orwig, Kyle E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803776/
https://www.ncbi.nlm.nih.gov/pubmed/28339678
http://dx.doi.org/10.1095/biolreprod.116.142828
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author Gassei, Kathrin
Sheng, Yi
Fayomi, Adetunji
Mital, Payal
Sukhwani, Meena
Lin, Chih-Cheng
Peters, Karen A.
Althouse, Andrew
Valli, Hanna
Orwig, Kyle E.
author_facet Gassei, Kathrin
Sheng, Yi
Fayomi, Adetunji
Mital, Payal
Sukhwani, Meena
Lin, Chih-Cheng
Peters, Karen A.
Althouse, Andrew
Valli, Hanna
Orwig, Kyle E.
author_sort Gassei, Kathrin
collection PubMed
description Spermatogonial stem cells (SSC) are essential for spermatogenesis and male fertility. In addition, these adult tissue stem cells can be used as vehicles for germline modification in animal models and may have application for treating male infertility. To facilitate the investigation of SSCs and germ lineage development in rats, we generated a DEAD-box helicase 4 (DDX4) (VASA) promoter-enhanced green fluorescent protein (EGFP) reporter transgenic rat. Quantitative real-time polymerase chain reaction and immunofluorescence confirmed that EGFP was expressed in the germ cells of the ovaries and testes and was absent in somatic cells and tissues. Germ cell transplantation demonstrated that the EGFP-positive germ cell population from DDX4-EGFP rat testes contained SSCs capable of establishing spermatogenesis in experimentally infertile mouse recipient testes. EGFP-positive germ cells could be easily isolated by fluorescence-activated cells sorting, while simultaneously removing testicular somatic cells from DDX4-EGFP rat pup testes. The EGFP-positive fraction provided an optimal cell suspension to establish rat SSC cultures that maintained long-term expression of zinc finger and BTB domain containing 16 (ZBTB16) and spalt-like transcription factor 4 (SALL4), two markers of mouse SSCs that are conserved in rats. The novel DDX4-EGFP germ cell reporter rat described here combined with previously described GCS-EGFP rats, rat SSC culture and gene editing tools will improve the utility of the rat model for studying stem cells and germ lineage development.
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spelling pubmed-58037762018-02-23 DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†) Gassei, Kathrin Sheng, Yi Fayomi, Adetunji Mital, Payal Sukhwani, Meena Lin, Chih-Cheng Peters, Karen A. Althouse, Andrew Valli, Hanna Orwig, Kyle E. Biol Reprod Testis Spermatogonial stem cells (SSC) are essential for spermatogenesis and male fertility. In addition, these adult tissue stem cells can be used as vehicles for germline modification in animal models and may have application for treating male infertility. To facilitate the investigation of SSCs and germ lineage development in rats, we generated a DEAD-box helicase 4 (DDX4) (VASA) promoter-enhanced green fluorescent protein (EGFP) reporter transgenic rat. Quantitative real-time polymerase chain reaction and immunofluorescence confirmed that EGFP was expressed in the germ cells of the ovaries and testes and was absent in somatic cells and tissues. Germ cell transplantation demonstrated that the EGFP-positive germ cell population from DDX4-EGFP rat testes contained SSCs capable of establishing spermatogenesis in experimentally infertile mouse recipient testes. EGFP-positive germ cells could be easily isolated by fluorescence-activated cells sorting, while simultaneously removing testicular somatic cells from DDX4-EGFP rat pup testes. The EGFP-positive fraction provided an optimal cell suspension to establish rat SSC cultures that maintained long-term expression of zinc finger and BTB domain containing 16 (ZBTB16) and spalt-like transcription factor 4 (SALL4), two markers of mouse SSCs that are conserved in rats. The novel DDX4-EGFP germ cell reporter rat described here combined with previously described GCS-EGFP rats, rat SSC culture and gene editing tools will improve the utility of the rat model for studying stem cells and germ lineage development. Oxford University Press 2017-03 2017-02-20 /pmc/articles/PMC5803776/ /pubmed/28339678 http://dx.doi.org/10.1095/biolreprod.116.142828 Text en © The Authors 2017. Published by Oxford University Press on behalf of Society for the Study of Reproduction. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Testis
Gassei, Kathrin
Sheng, Yi
Fayomi, Adetunji
Mital, Payal
Sukhwani, Meena
Lin, Chih-Cheng
Peters, Karen A.
Althouse, Andrew
Valli, Hanna
Orwig, Kyle E.
DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)
title DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)
title_full DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)
title_fullStr DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)
title_full_unstemmed DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)
title_short DDX4-EGFP transgenic rat model for the study of germline development and spermatogenesis (†)
title_sort ddx4-egfp transgenic rat model for the study of germline development and spermatogenesis (†)
topic Testis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5803776/
https://www.ncbi.nlm.nih.gov/pubmed/28339678
http://dx.doi.org/10.1095/biolreprod.116.142828
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