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Updated: Aug 6, 2026

Serial Enrichment of Spermatogonial Stem and Progenitor Cells (SSCs) in Culture for Derivation of Long-term Adult Mouse SSC Lines
Published on: February 25, 2013
[Proliferation and undifferentiation of spermatogonial stem cells in vitro]
Fu-cui Xu1, Shao-hua Wu, Yong Guo
1Department of Histology and Embryology, Luzhou Medical College, Luzhou 646000, China.
Objective:
To investigate the fluences on the proliferation and undifferentiation of spermatogonial stem cells in vitro.
Methods:
Mouse bone marrow stromal cells were subjected to primary culture; when the cells grew up and extended around, they were treated with mitomycin C. And then, to the bone marrow stromal cells were added spermatogonial stem cells for co-culture. The ambient temperature was 37 degrees C.
Results:
The spermatogonial stem cells increased in number obviously when cultured for 2-4 days, they could be single, paired or clustered, while the differentiated cells began to die; when cultured for 4-8 days, the cells proliferated not in a distinct manner, they seemed to be stable; but at 10 days, the cells began to grow, especially when cultured for 15 days, the cells had the characteristic structure of the spermatogonial stem cell; when cultured continuously for 25 days, the cells had the same morphology and very clear intercellular bridges.
Conclusion:
Spermatogonial stem cells can proliferate and continue to be undifferentiated on the bone marrow stromal cells when the ambient temperature is 37 degrees C.
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