Abstract
The in vitro propagation of mouse spermatogonial stem cells (SSCs) became possible in 2003; these cultured SSCs were named germ-line stem (GS) cells. To date, however, it has not been possible to induce spermatogenesis from GS cells in vitro. Recently, we succeeded in producing functional sperm from primitive spermatogonia in explanted neonatal mouse testis tissues. Here we describe a protocol that can support spermatogenesis from GS cells up to sperm formation in vitro using an organ culture method. GS cells transplanted in the extracted testis form colonies in the tissue fragments and differentiate into sperm under the described in vitro organ culture conditions. It takes about 6 weeks to obtain sperm from GS cells. The sperm are viable, resulting in healthy offspring through micro-insemination. Thus, this protocol should be a valuable tool for the study of mammalian spermatogenesis.
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Acknowledgements
This work was supported by a Grant-in-Aid for Scientific Research on Innovative Areas, 'Regulatory Mechanism of Gamete Stem Cells' 20116005 (to T.O.); a Grant-in-Aid for Scientific Research (B) 24390371 (to T.O.); a Grant-in-Aid for Young Scientists (B) 24770216 (to T.S.); a grant for Research and Development Project II of Yokohama City University (to T.O.); and a grant for Establishment of Research Center for Clinical Proteomics of Post-translational Modifications (to T.O.).
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T.S., K.K. and T.O. wrote the manuscript. Y.K. supervised the research.
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Supplementary Video 1
In vitro transplantation procedure. Preparation of testis, dissociation of efferent ducts, insertion of glass needle, and injection of dye solution into the rete cavity, which spread into the lumen of the seminiferous tubules. (MOV 10100 kb)
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Sato, T., Katagiri, K., Kubota, Y. et al. In vitro sperm production from mouse spermatogonial stem cell lines using an organ culture method. Nat Protoc 8, 2098–2104 (2013). https://doi.org/10.1038/nprot.2013.138
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DOI: https://doi.org/10.1038/nprot.2013.138
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