Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cell Cycle. 2013 Aug 15;12(16):2538-45. doi: 10.4161/cc.25627. Epub 2013 Jul 10.
Gonocytes (or prospermatogonia) are the precursors to spermatogonial stem cells (SSCs), which provide the foundation for spermatogenesis through their ability to both self-renew and generate daughter cells. Despite their relative importance, the regulatory mechanisms that govern gonocyte maintenance and transition to SSCs are poorly understood. Recently, we reported that constitutive activation of NOTCH1 signaling in Sertoli cells causes gonocyte exit from quiescence--the first suggestion of the potential role of this signaling pathway in the testis. This Extra View will review what is known about NOTCH signaling, particularly in Sertoli cells and germ cells in the testes, by providing a background on germ cell biology and a summary of our recently published data on NOTCH1 signaling in Sertoli cells. We also describe additional data showing that aberrant proliferation and differentiation of gonocytes in response to constitutive activation of NOTCH1 signaling in Sertoli cells involves de novo expression of cell cycle proteins and a marked upregulation of the KIT receptor. These data further suggest that NOTCH signaling orchestrates a dynamic balance between maintenance and differentiation of gonocytes in the perinatal testis.
精原细胞(或生殖母细胞)是精原干细胞(SSC)的前体细胞,通过自我更新和产生子细胞的能力为精子发生提供基础。尽管它们相对重要,但调控精原细胞维持和向 SSC 分化的机制仍知之甚少。最近,我们报道了在支持细胞中组成性激活 NOTCH1 信号会导致精原细胞退出静止状态——这首次提示该信号通路可能在睾丸中发挥作用。本篇专文将通过提供生殖细胞生物学背景知识,并总结我们最近发表的关于支持细胞中 NOTCH1 信号的研究数据,来综述已知的关于 NOTCH 信号通路的知识,特别是在睾丸中的支持细胞和生殖细胞中。我们还描述了额外的数据,表明支持细胞中 NOTCH1 信号的组成性激活会导致精原细胞异常增殖和分化,这涉及到细胞周期蛋白的新表达和 KIT 受体的显著上调。这些数据进一步表明,NOTCH 信号在围产期睾丸中精原细胞的维持和分化之间协调了一种动态平衡。