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National Journal of Andrology ; (12): 695-700, 2008.
Artículo en Chino | WPRIM | ID: wpr-309812

RESUMEN

<p><b>OBJECTIVE</b>To establish a long-term proliferation culture system for mouse spermatogonial stem cells.</p><p><b>METHODS</b>Testis tissues were obtained from 30 newborn male ICR mice on postnatal day 2-6. Testis cell suspension was collected by two-step enzymatic digestion prior to culture. The dissociated cells were aliquoted into tissue culture plates and cultivated with a modified system composed of serum-free defined medium on mouse embryonic fibroblasts (MEF) feeders. Their proliferation was determined by the BrdU incorporation test and the cultured cells identified by alkaline phosphatase (AP) activity, immunofluorescence staining and RT-PCR assay.</p><p><b>RESULTS</b>The cultures remained in a steady state and continued to generate germ cell colonies. The undifferentiated state was confirmed by strong positivity for AP activity, immunofluorescent staining of GFRalpha-1+ /Oct-4+ /VASA+ /SCP3- and GFRalpha-1+ /Oct-4+/SCP3- at the gene expression levels.</p><p><b>CONCLUSION</b>Mouse spermatogonial stem cells could be expanded in our defined culture system and passaged steadily in vitro. The harvested cells remained in an undifferentiated state, which has provided a good platform for the study of spermatogenesis in vitro.</p>


Asunto(s)
Animales , Masculino , Ratones , Fosfatasa Alcalina , Genética , Metabolismo , Técnicas de Cultivo de Célula , Proliferación Celular , Células Cultivadas , Técnica del Anticuerpo Fluorescente , Ratones Endogámicos ICR , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Espermatogonias , Biología Celular , Metabolismo , Células Madre , Biología Celular , Metabolismo , Factores de Tiempo
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