Wu Zhuoru, Luby-Phelps Katherine, Bugde Abhijit, Molyneux Laura A, Denard Bray, Li Wen-Hong, Süel Gürol M, Garbers David L
Cecil H. and Ida Green Center for Reproductive Biology Sciences, Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
J Cell Biol. 2009 Nov 16;187(4):513-24. doi: 10.1083/jcb.200907047. Epub 2009 Nov 9.
Mammalian spermatogenesis is initiated and sustained by spermatogonial stem cells (SSCs) through self-renewal and differentiation. The basic question of whether SSCs have the potential to specify self-renewal and differentiation in a cell-autonomous manner has yet to be addressed. Here, we show that rat SSCs in ex vivo culture conditions consistently give rise to two distinct types of progeny: new SSCs and differentiating germ cells, even when they have been exposed to virtually identical microenvironments. Quantitative experimental measurements and mathematical modeling indicates that fate decision is stochastic, with constant probability. These results reveal an unexpected ability in a mammalian SSC to specify both self-renewal and differentiation through a self-directed mechanism, and further suggest that this mechanism operates according to stochastic principles. These findings provide an experimental basis for autonomous and stochastic fate choice as an alternative strategy for SSC fate bifurcation, which may also be relevant to other stem cell types.
哺乳动物的精子发生由精原干细胞(SSCs)通过自我更新和分化启动并维持。SSCs是否具有以细胞自主方式确定自我更新和分化的潜力这一基本问题尚未得到解决。在这里,我们表明,即使在几乎相同的微环境中,体外培养条件下的大鼠SSCs始终会产生两种不同类型的后代:新的SSCs和正在分化的生殖细胞。定量实验测量和数学建模表明,命运决定是随机的,具有恒定的概率。这些结果揭示了哺乳动物SSC具有通过自我导向机制确定自我更新和分化的意外能力,并进一步表明该机制根据随机原则运作。这些发现为自主和随机命运选择作为SSC命运分叉的替代策略提供了实验依据,这也可能与其他干细胞类型相关。