Ikami Kanako, Tokue Moe, Sugimoto Ryo, Noda Chiyo, Kobayashi Satoru, Hara Kenshiro, Yoshida Shosei
Division of Germ Cell Biology, National Institute for Basic Biology, National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki 444-8787, Japan Department of Basic Biology, School of Life Science, Graduate University for Advanced Studies (Sokendai), 5-1 Higashiyama, Myodaiji, Okazaki 444-8787, Japan.
Division of Germ Cell Biology, National Institute for Basic Biology, National Institutes of Natural Sciences, 5-1 Higashiyama, Myodaiji, Okazaki 444-8787, Japan.
Development. 2015 May 1;142(9):1582-92. doi: 10.1242/dev.118695. Epub 2015 Apr 9.
Stem cells ensure tissue homeostasis through the production of differentiating and self-renewing progeny. In some tissues, this is achieved by the function of a definitive stem cell niche. However, the mechanisms that operate in mouse spermatogenesis are unknown because undifferentiated spermatogonia (Aundiff) are motile and intermingle with differentiating cells in an 'open' niche environment of seminiferous tubules. Aundiff include glial cell line-derived neurotrophic factor receptor α1 (GFRα1)(+) and neurogenin 3 (NGN3)(+) subpopulations, both of which retain the ability to self-renew. However, whereas GFRα1(+) cells comprise the homeostatic stem cell pool, NGN3(+) cells show a higher probability to differentiate into KIT(+) spermatogonia by as yet unknown mechanisms. In the present study, by combining fate analysis of pulse-labeled cells and a model of vitamin A deficiency, we demonstrate that retinoic acid (RA), which may periodically increase in concentration in the tubules during the seminiferous epithelial cycle, induced only NGN3(+) cells to differentiate. Comparison of gene expression revealed that retinoic acid receptor γ (Rarg) was predominantly expressed in NGN3(+) cells, but not in GFRα1(+) cells, whereas the expression levels of many other RA response-related genes were similar in the two populations. Ectopic expression of RARγ was sufficient to induce GFRα1(+) cells to directly differentiate to KIT(+) cells without transiting the NGN3(+) state. Therefore, RARγ plays key roles in the differentiation competence of NGN3(+) cells. We propose a novel mechanism of stem cell fate selection in an open niche environment whereby undifferentiated cells show heterogeneous competence to differentiate in response to ubiquitously distributed differentiation-inducing signals.
干细胞通过产生分化和自我更新的子代细胞来确保组织稳态。在某些组织中,这是通过明确的干细胞微环境的功能来实现的。然而,在小鼠精子发生过程中起作用的机制尚不清楚,因为未分化的精原细胞(Aundiff)具有运动能力,并在生精小管的“开放”微环境中与分化细胞相互混合。Aundiff包括胶质细胞系衍生的神经营养因子受体α1(GFRα1)(+)和神经生成素3(NGN3)(+)亚群,两者都保留自我更新的能力。然而,虽然GFRα1(+)细胞构成了稳态干细胞池,但NGN3(+)细胞通过尚未明确的机制显示出更高的分化为KIT(+)精原细胞的概率。在本研究中,通过结合脉冲标记细胞的命运分析和维生素A缺乏模型,我们证明视黄酸(RA),其在生精上皮周期中可能在小管中周期性地增加浓度,仅诱导NGN3(+)细胞分化。基因表达比较显示,视黄酸受体γ(Rarg)主要在NGN3(+)细胞中表达,而不在GFRα1(+)细胞中表达,而许多其他与RA反应相关的基因在这两个群体中的表达水平相似。RARγ的异位表达足以诱导GFRα1(+)细胞直接分化为KIT(+)细胞,而无需经过NGN3(+)状态。因此,RARγ在NGN3(+)细胞的分化能力中起关键作用。我们提出了一种在开放微环境中干细胞命运选择的新机制,即未分化细胞对普遍分布的分化诱导信号表现出异质性的分化能力。