Yan Kelley S, Gevaert Olivier, Zheng Grace X Y, Anchang Benedict, Probert Christopher S, Larkin Kathryn A, Davies Paige S, Cheng Zhuan-Fen, Kaddis John S, Han Arnold, Roelf Kelly, Calderon Ruben I, Cynn Esther, Hu Xiaoyi, Mandleywala Komal, Wilhelmy Julie, Grimes Sue M, Corney David C, Boutet Stéphane C, Terry Jessica M, Belgrader Phillip, Ziraldo Solongo B, Mikkelsen Tarjei S, Wang Fengchao, von Furstenberg Richard J, Smith Nicholas R, Chandrakesan Parthasarathy, May Randal, Chrissy Mary Ann S, Jain Rajan, Cartwright Christine A, Niland Joyce C, Hong Young-Kwon, Carrington Jill, Breault David T, Epstein Jonathan, Houchen Courtney W, Lynch John P, Martin Martin G, Plevritis Sylvia K, Curtis Christina, Ji Hanlee P, Li Linheng, Henning Susan J, Wong Melissa H, Kuo Calvin J
Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA; Columbia Center for Human Development, Columbia Stem Cell Initiative, Department of Medicine, Division of Digestive and Liver Diseases, Department of Genetics and Development, Columbia University Medical Center, New York, NY 10032, USA.
Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Cell Stem Cell. 2017 Jul 6;21(1):78-90.e6. doi: 10.1016/j.stem.2017.06.014.
Several cell populations have been reported to possess intestinal stem cell (ISC) activity during homeostasis and injury-induced regeneration. Here, we explored inter-relationships between putative mouse ISC populations by comparative RNA-sequencing (RNA-seq). The transcriptomes of multiple cycling ISC populations closely resembled Lgr5 ISCs, the most well-defined ISC pool, but Bmi1-GFP cells were distinct and enriched for enteroendocrine (EE) markers, including Prox1. Prox1-GFP cells exhibited sustained clonogenic growth in vitro, and lineage-tracing of Prox1 cells revealed long-lived clones during homeostasis and after radiation-induced injury in vivo. Single-cell mRNA-seq revealed two subsets of Prox1-GFP cells, one of which resembled mature EE cells while the other displayed low-level EE gene expression but co-expressed tuft cell markers, Lgr5 and Ascl2, reminiscent of label-retaining secretory progenitors. Our data suggest that the EE lineage, including mature EE cells, comprises a reservoir of homeostatic and injury-inducible ISCs, extending our understanding of cellular plasticity and stemness.
据报道,在稳态和损伤诱导的再生过程中,有几种细胞群具有肠道干细胞(ISC)活性。在这里,我们通过比较RNA测序(RNA-seq)探索了假定的小鼠ISC群体之间的相互关系。多个循环ISC群体的转录组与定义最明确的ISC库Lgr5 ISC非常相似,但Bmi1-GFP细胞是不同的,并且富含肠内分泌(EE)标志物,包括Prox1。Prox1-GFP细胞在体外表现出持续的克隆生长,并且对Prox1细胞进行谱系追踪揭示了在体内稳态期间和辐射诱导损伤后存在长寿克隆。单细胞mRNA-seq揭示了Prox1-GFP细胞的两个亚群,其中一个类似于成熟的EE细胞,而另一个显示低水平的EE基因表达,但共同表达簇细胞标志物、Lgr5和Ascl2,让人联想到标记保留分泌祖细胞。我们的数据表明,包括成熟EE细胞在内的EE谱系包含稳态和损伤诱导性ISC的储存库,扩展了我们对细胞可塑性和干性的理解。