Buageaw Anyanee, Sukhwani Meena, Ben-Yehudah Ahmi, Ehmcke Jens, Rawe Vanesa Y, Pholpramool Chumpol, Orwig Kyle E, Schlatt Stefan
Department of Physiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Biol Reprod. 2005 Nov;73(5):1011-6. doi: 10.1095/biolreprod.105.043810. Epub 2005 Jul 13.
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 alpha1 (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.
精原干细胞(SSCs)对精子发生至关重要,这些成体组织干细胞平衡自我更新和分化以满足睾丸的生物学需求。SSCs的发育动态部分受干细胞微环境中的因子控制,该微环境位于支持细胞之间的生精小管基底膜上。支持细胞产生胶质细胞系源性神经营养因子(GDNF),GDNF表达的破坏会导致生精缺陷和不育。GDNF通过包括GDNF家族受体α1(GFRA1)的受体复合物发出信号,GFRA1被认为由SSCs表达。然而,GFRA1在SSCs上的表达尚未通过体内功能测定得到证实,而体内功能测定是唯一能够明确鉴定SSCs的方法。因此,我们使用磁激活细胞分选基于GFRA1表达对小鼠幼崽睾丸细胞进行了分选。通过免疫细胞化学对GFRA1分选和耗尽的部分进行生殖细胞标志物鉴定,并通过生殖细胞移植对干细胞活性进行鉴定。GFRA1阳性细胞部分与包括ITGA6和CD9在内的SSCs其他标志物共洗脱,并且KIT阳性细胞显著减少。移植结果证实了SSCs的一个亚群表达GFRA1,但干细胞库在GFRA1表达水平方面也是异质性的。有趣的是,POU5F1阳性细胞在GFRA1选择的部分中富集了近15倍,这可能表明干细胞库内发育潜能的异质性。