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Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction

Generation of germ cells from pluripotent stem cells in vitro could have great application for treating infertility and provides an excellent model for uncovering molecular mechanisms controlling gametogenesis. In this study, we explored the differentiation potential of mouse induced pluripotent ste...

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Autores principales: Li, Peng, Hu, Hongliang, Yang, Shi, Tian, Ruhui, Zhang, Zhenzhen, Zhang, Wei, Ma, Meng, Zhu, Yong, Guo, Xizhi, Huang, Yiran, He, Zuping, Li, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591174/
https://www.ncbi.nlm.nih.gov/pubmed/23509752
http://dx.doi.org/10.1155/2013/608728
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author Li, Peng
Hu, Hongliang
Yang, Shi
Tian, Ruhui
Zhang, Zhenzhen
Zhang, Wei
Ma, Meng
Zhu, Yong
Guo, Xizhi
Huang, Yiran
He, Zuping
Li, Zheng
author_facet Li, Peng
Hu, Hongliang
Yang, Shi
Tian, Ruhui
Zhang, Zhenzhen
Zhang, Wei
Ma, Meng
Zhu, Yong
Guo, Xizhi
Huang, Yiran
He, Zuping
Li, Zheng
author_sort Li, Peng
collection PubMed
description Generation of germ cells from pluripotent stem cells in vitro could have great application for treating infertility and provides an excellent model for uncovering molecular mechanisms controlling gametogenesis. In this study, we explored the differentiation potential of mouse induced pluripotent stem (iPS) cells towards male germ cells. Embryoid body formation and retinoic acid/testosterone induction were applied to promote differentiation of mouse iPS cells into male germ cells in vitro. Quantitative RT-PCR and immunoflourescence were performed to characterize the iPS cell differentiation process, and notably there were different temporal expression profiles of male germ cell-associated genes. The expression of proteins, including MVH, CDH1, and SCP3, was remarkably increased. mRNA expression of Stra8, Odf2, Act, and Prm1 was upregulated in iPS cells by retinoic acid or testosterone induction, whereas Oct-4 transcription was reduced in these cells compared to the controls. Hormones were also measured in the EB medium. DNA content analysis by flow cytometry revealed that iPS cells could differentiate into haploid cells through retinoic acid or testosterone treatment. Collectively, our results suggest that mouse iPS cells possess the potency to differentiate into male germ cells in vitro through embryoid body formation and retinoic acid or testosterone induction.
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spelling pubmed-35911742013-03-18 Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction Li, Peng Hu, Hongliang Yang, Shi Tian, Ruhui Zhang, Zhenzhen Zhang, Wei Ma, Meng Zhu, Yong Guo, Xizhi Huang, Yiran He, Zuping Li, Zheng Biomed Res Int Research Article Generation of germ cells from pluripotent stem cells in vitro could have great application for treating infertility and provides an excellent model for uncovering molecular mechanisms controlling gametogenesis. In this study, we explored the differentiation potential of mouse induced pluripotent stem (iPS) cells towards male germ cells. Embryoid body formation and retinoic acid/testosterone induction were applied to promote differentiation of mouse iPS cells into male germ cells in vitro. Quantitative RT-PCR and immunoflourescence were performed to characterize the iPS cell differentiation process, and notably there were different temporal expression profiles of male germ cell-associated genes. The expression of proteins, including MVH, CDH1, and SCP3, was remarkably increased. mRNA expression of Stra8, Odf2, Act, and Prm1 was upregulated in iPS cells by retinoic acid or testosterone induction, whereas Oct-4 transcription was reduced in these cells compared to the controls. Hormones were also measured in the EB medium. DNA content analysis by flow cytometry revealed that iPS cells could differentiate into haploid cells through retinoic acid or testosterone treatment. Collectively, our results suggest that mouse iPS cells possess the potency to differentiate into male germ cells in vitro through embryoid body formation and retinoic acid or testosterone induction. Hindawi Publishing Corporation 2013 2012-12-30 /pmc/articles/PMC3591174/ /pubmed/23509752 http://dx.doi.org/10.1155/2013/608728 Text en Copyright © 2013 Peng Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Peng
Hu, Hongliang
Yang, Shi
Tian, Ruhui
Zhang, Zhenzhen
Zhang, Wei
Ma, Meng
Zhu, Yong
Guo, Xizhi
Huang, Yiran
He, Zuping
Li, Zheng
Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction
title Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction
title_full Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction
title_fullStr Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction
title_full_unstemmed Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction
title_short Differentiation of Induced Pluripotent Stem Cells into Male Germ Cells In Vitro through Embryoid Body Formation and Retinoic Acid or Testosterone Induction
title_sort differentiation of induced pluripotent stem cells into male germ cells in vitro through embryoid body formation and retinoic acid or testosterone induction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591174/
https://www.ncbi.nlm.nih.gov/pubmed/23509752
http://dx.doi.org/10.1155/2013/608728
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