Publication:
GDNF family receptor alpha1 phenotype of spermatogonial stem cells in immature mouse testes

dc.contributor.authorAnyanee Buageawen_US
dc.contributor.authorMeena Sukhwanien_US
dc.contributor.authorAhmi Ben-Yehudahen_US
dc.contributor.authorJens Ehmckeen_US
dc.contributor.authorVanesa Y. Raween_US
dc.contributor.authorChumpol Pholpramoolen_US
dc.contributor.authorKyle E. Orwigen_US
dc.contributor.authorStefan Schlatten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.contributor.otherUniversity of Pittsburgh School of Medicineen_US
dc.contributor.otherMagee-Womens Research Instituteen_US
dc.date.accessioned2018-06-21T08:07:46Z
dc.date.available2018-06-21T08:07:46Z
dc.date.issued2005-11-01en_US
dc.description.abstractSpermatogonial stem cells (SSCs) are essential for spermatogenesis, and these adult tissue stem cells balance self-renewal and differentiation to meet the biological demand of the testis. The developmental dynamics of SSCs are controlled, in part, by factors in the stem cell niche, which is located on the basement membrane of seminiferous tubules situated among Sertoli cells. Sertoli cells produce glial cell line-derived neurotrophic factor (GDNF), and disruption of GDNF expression results in spermatogenic defects and infertility. The GDNF signals through a receptor complex that includes GDNF family receptor α1 (GFRA1), which is thought to be expressed by SSCs. However, expression of GFRA1 on SSCs has not been confirmed by in vivo functional assay, which is the only method that allows definitive identification of SSCs. Therefore, we fractionated mouse pup testis cells based on GFRA1 expression using magnetic activated cell sorting. The sorted and depleted fractions of GFRA1 were characterized for germ cell markers by immunocytochemistry and for stem cell activity by germ cell transplantation. The GFRA1-positive cell fraction coeluted with other markers of SSCs, including ITGA6 and CD9, and was significantly depleted of KIT-positive cells. The transplantation results confirmed that a subpopulation of SSCs expresses GFRA1, but also that the stem cell pool is heterogeneous with respect to the level of GFRA1 expression. Interestingly, POU5F1-positive cells were enriched nearly 15-fold in the GFRA1-selected fraction, possibly suggesting heterogeneity of developmental potential within the stem cell pool. © 2005 by the Society for the Study of Reproduction, Inc.en_US
dc.identifier.citationBiology of Reproduction. Vol.73, No.5 (2005), 1011-1016en_US
dc.identifier.doi10.1095/biolreprod.105.043810en_US
dc.identifier.issn00063363en_US
dc.identifier.other2-s2.0-27144528526en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/16278
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27144528526&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleGDNF family receptor alpha1 phenotype of spermatogonial stem cells in immature mouse testesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=27144528526&origin=inwarden_US

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