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

被引:161
|
作者
Buageaw, A
Sukhwani, M
Ben-Yehudah, A
Ehmcke, J
Rawe, VY
Pholpramool, C
Orwig, KE
Schlatt, S
机构
[1] Univ Pittsburgh, Sch Med, Dept Cell Biol & Physiol, Ctr Res Reprod Physiol, Pittsburgh, PA 15261 USA
[2] Mahidol Univ, Fac Sci, Dept Physiol, Bangkok 10400, Thailand
[3] Mahidol Univ, Inst Sci & Technol Res & Dev, Nakhon Pathom 73170, Thailand
[4] Univ Pittsburgh, Sch Med, Pittsburgh Dev Ctr Magee Womens Res Inst, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Sch Med, Pittsburgh Dev Ctr Magee Womens Res Inst, Dept Mol Genet & Biochem, Pittsburgh, PA 15213 USA
关键词
gamete biology; spermatogenesis; testis;
D O I
10.1095/biolreprod.105.043810
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Spermatogonial 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 alpha 1 (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.
引用
收藏
页码:1011 / 1016
页数:6
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