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Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation

Spermatogonial stem cells (SSCs) have significant applications in both reproductive and regenerative medicine. However, primary human SSCs are very rare, and a human SSC line has not yet been available. In this study, we have for the first time reported a stable human SSC line by stably expressing h...

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Autores principales: Hou, Jingmei, Niu, Minghui, Liu, Linhong, Zhu, Zijue, Wang, Xiaobo, Sun, Min, Yuan, Qingqing, Yang, Shi, Zeng, Wenxian, Liu, Yang, Li, Zheng, He, Zuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653657/
https://www.ncbi.nlm.nih.gov/pubmed/26585066
http://dx.doi.org/10.1038/srep16922
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author Hou, Jingmei
Niu, Minghui
Liu, Linhong
Zhu, Zijue
Wang, Xiaobo
Sun, Min
Yuan, Qingqing
Yang, Shi
Zeng, Wenxian
Liu, Yang
Li, Zheng
He, Zuping
author_facet Hou, Jingmei
Niu, Minghui
Liu, Linhong
Zhu, Zijue
Wang, Xiaobo
Sun, Min
Yuan, Qingqing
Yang, Shi
Zeng, Wenxian
Liu, Yang
Li, Zheng
He, Zuping
author_sort Hou, Jingmei
collection PubMed
description Spermatogonial stem cells (SSCs) have significant applications in both reproductive and regenerative medicine. However, primary human SSCs are very rare, and a human SSC line has not yet been available. In this study, we have for the first time reported a stable human SSC line by stably expressing human SV40 large T antigen. RT-PCR, immunocytochemistry, and Western blots revealed that this cell line was positive for a number of human spermatogonial and SSC hallmarks, including VASA, DAZL, MAGEA4, GFRA1, RET, UCHL1, GPR125, PLZF and THY1, suggesting that these cells are human SSCs phenotypically. Proliferation analysis showed that the cell line could be expanded with significant increases of cells for 1.5 years, and high levels of PCNA, UCHL1 and SV40 were maintained for long-term culture. Transplantation assay indicated that human SSC line was able to colonize and proliferate in vivo in the recipient mice. Neither Y chromosome microdeletions of numerous genes nor tumor formation was observed in human SSC line although there was abnormal karyotype in this cell line. Collectively, we have established a human SSC line with unlimited proliferation potentials and no tumorgenesis, which could provide an abundant source of human SSCs for their mechanistic studies and translational medicine.
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spelling pubmed-46536572015-11-25 Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation Hou, Jingmei Niu, Minghui Liu, Linhong Zhu, Zijue Wang, Xiaobo Sun, Min Yuan, Qingqing Yang, Shi Zeng, Wenxian Liu, Yang Li, Zheng He, Zuping Sci Rep Article Spermatogonial stem cells (SSCs) have significant applications in both reproductive and regenerative medicine. However, primary human SSCs are very rare, and a human SSC line has not yet been available. In this study, we have for the first time reported a stable human SSC line by stably expressing human SV40 large T antigen. RT-PCR, immunocytochemistry, and Western blots revealed that this cell line was positive for a number of human spermatogonial and SSC hallmarks, including VASA, DAZL, MAGEA4, GFRA1, RET, UCHL1, GPR125, PLZF and THY1, suggesting that these cells are human SSCs phenotypically. Proliferation analysis showed that the cell line could be expanded with significant increases of cells for 1.5 years, and high levels of PCNA, UCHL1 and SV40 were maintained for long-term culture. Transplantation assay indicated that human SSC line was able to colonize and proliferate in vivo in the recipient mice. Neither Y chromosome microdeletions of numerous genes nor tumor formation was observed in human SSC line although there was abnormal karyotype in this cell line. Collectively, we have established a human SSC line with unlimited proliferation potentials and no tumorgenesis, which could provide an abundant source of human SSCs for their mechanistic studies and translational medicine. Nature Publishing Group 2015-11-20 /pmc/articles/PMC4653657/ /pubmed/26585066 http://dx.doi.org/10.1038/srep16922 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hou, Jingmei
Niu, Minghui
Liu, Linhong
Zhu, Zijue
Wang, Xiaobo
Sun, Min
Yuan, Qingqing
Yang, Shi
Zeng, Wenxian
Liu, Yang
Li, Zheng
He, Zuping
Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation
title Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation
title_full Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation
title_fullStr Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation
title_full_unstemmed Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation
title_short Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation
title_sort establishment and characterization of human germline stem cell line with unlimited proliferation potentials and no tumor formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653657/
https://www.ncbi.nlm.nih.gov/pubmed/26585066
http://dx.doi.org/10.1038/srep16922
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