Centre for Craniofacial and Regenerative Biology, Dental Institute, Kings College, London, UK.
Center for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA, USA.
Cell Rep. 2018 Jun 5;23(10):3102-3111. doi: 10.1016/j.celrep.2018.05.001.
In adult tissues and organs with high turnover rates, the generation of transit-amplifying cell (TAC) populations from self-renewing stem cells drives cell replacement. The role of stem cells is to provide a renewable source of cells that give rise to TACs to provide the cell numbers that are necessary for cell differentiation. Regulation of the formation of TACs is thus fundamental to controlling cell replacement. Here, we analyze the properties of a population of mesenchymal TACs in the continuously growing mouse incisor to identify key components of the molecular regulation that drives proliferation. We show that the polycomb repressive complex 1 acts as a global regulator of the TAC phenotype by its direct action on the expression of key cell-cycle regulatory genes and by regulating Wnt/β-catenin-signaling activity. We also identify an essential requirement for TACs in maintaining mesenchymal stem cells, which is indicative of a positive feedback mechanism.
在具有高周转率的成人组织和器官中,自我更新的干细胞产生过渡扩增细胞 (TAC) 群体,从而驱动细胞替换。干细胞的作用是提供可产生 TAC 的可再生细胞源,以提供细胞分化所需的细胞数量。因此,TAC 形成的调控对于控制细胞替换至关重要。在这里,我们分析了在不断生长的小鼠切牙中的一群间充质 TAC 的特性,以鉴定驱动增殖的分子调控的关键组成部分。我们表明,多梳抑制复合物 1 通过其对关键细胞周期调节基因表达的直接作用以及通过调节 Wnt/β-catenin 信号活性,作为 TAC 表型的全局调节剂。我们还发现 TAC 对于维持间充质干细胞是必需的,这表明存在正反馈机制。