Seidel Kerstin, Marangoni Pauline, Tang Cynthia, Houshmand Bahar, Du Wen, Maas Richard L, Murray Steven, Oldham Michael C, Klein Ophir D
Department of Orofacial Sciences and Program in Craniofacial Biology, University of California, San Francisco, San Francisco, United States.
Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, United States.
Elife. 2017 May 5;6:e24712. doi: 10.7554/eLife.24712.
Investigations into stem cell-fueled renewal of an organ benefit from an inventory of cell type-specific markers and a deep understanding of the cellular diversity within stem cell niches. Using the adult mouse incisor as a model for a continuously renewing organ, we performed an unbiased analysis of gene co-expression relationships to identify modules of co-expressed genes that represent differentiated cells, transit-amplifying cells, and residents of stem cell niches. Through in vivo lineage tracing, we demonstrated the power of this approach by showing that co-expression module members and define populations of incisor epithelial and mesenchymal stem cells. We further discovered that two adjacent mesenchymal tissues, the periodontium and dental pulp, are maintained by distinct pools of stem cells. These findings reveal novel mechanisms of incisor renewal and illustrate how gene co-expression analysis of intact biological systems can provide insights into the transcriptional basis of cellular identity.
对由干细胞驱动的器官更新进行研究,受益于细胞类型特异性标志物清单以及对干细胞龛内细胞多样性的深入了解。利用成年小鼠切牙作为持续更新器官的模型,我们对基因共表达关系进行了无偏分析,以识别代表分化细胞、过渡扩增细胞和干细胞龛驻留细胞的共表达基因模块。通过体内谱系追踪,我们通过表明共表达模块成员定义了切牙上皮和间充质干细胞群体,证明了这种方法的有效性。我们进一步发现,两个相邻的间充质组织,即牙周组织和牙髓,由不同的干细胞池维持。这些发现揭示了切牙更新的新机制,并说明了完整生物系统的基因共表达分析如何能够深入了解细胞身份的转录基础。
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