10
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Long-Term Propagation of Porcine Undifferentiated Spermatogonia

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Spermatogonial stem cells (SSCs) provide the foundation for spermatogenesis and fertility throughout the adult life of a male. Genetic manipulations of SSCs combined with germ cell transplantation present a novel approach for gene therapy and production of genetically modified animals. However, the rarity of SSCs within mammalian testes remains an impediment to related applications, making in vitro expansion of SSCs a prerequisite. Nevertheless, long-term culture systems of SSCs from large animals have not been established yet. In this study, we developed an optimized in vitro culture condition for porcine undifferentiated spermatogonia. The germ cells were isolated and enriched from 7-day-old porcine testes by an optimized differential planting. We tested different feeder layers and found that neonatal autologous Sertoli cells acted better than the SIM mouse embryo-derived thioguanine- and ouabain-resistant (STO) cell line and adult Sertoli cells. The effects of several growth factors were also investigated. Using neonatal Sertoli cells as feeder and Dulbecco's modified eagle medium: nutrient mixture F-12 (DMEM/F12) culture medium supplemented with 10% KSR and four cytokines, the undifferentiated spermatogonia can proliferate in vitro for at least 2 months without loss of stemness. The expression of SSC markers indicated that the cultured cells maintained SSC expression profiles. Moreover, xenotransplantation and in vitro induction showed that the long-term cultured cells preserved the capacity to colonize in vivo and differentiate in vitro, respectively, demonstrating the presence of SSCs in the cultured cells. In conclusion, the conditions described in this study can support the normal proliferation of porcine undifferentiated spermatogonia with stemness and normal karyotype for at least 2 months. This culture system will serve as a basic refinement in the future studies and facilitate studies on SSC biology and genetic manipulation of male germ cells.

          Related collections

          Author and article information

          Journal
          Stem Cells Dev
          Stem Cells Dev
          scd
          Stem Cells and Development
          Mary Ann Liebert, Inc. (140 Huguenot Street, 3rd FloorNew Rochelle, NY 10801USA )
          1547-3287
          1557-8534
          01 August 2017
          01 August 2017
          : 26
          : 15
          : 1121-1131
          Affiliations
          [ 1 ]College of Animal Science and Technology, Northwest A&F University , Shaanxi, China.
          [ 2 ]Center for Reproductive Medicine, Amsterdam Research Institute Reproduction and Development, Academic Medical Centre, University of Amsterdam , Amsterdam, the Netherlands.
          Author notes
          Address correspondence to: Prof. Wenxian Zeng, College of Animal Science and Technology, Northwest A&F University No. 22 Xi-nong Road, Yangling, Shaanxi 712100, China

          E-mail: zengwenxian2015@ 123456126.com
          Article
          PMC5563923 PMC5563923 5563923 10.1089/scd.2017.0018
          10.1089/scd.2017.0018
          5563923
          28474535
          c84892ce-de1a-4f9e-883f-81292f4c9482
          Copyright 2017, Mary Ann Liebert, Inc.
          History
          : 22 January 2017
          : 04 May 2017
          Page count
          Figures: 8, Tables: 1, References: 55, Pages: 11
          Categories
          Original Research Reports

          transplantation,cell culture,growth factor,spermatogonial stem cell,swine

          Comments

          Comment on this article