生物
转录组
干细胞
LGR5型
人口
细胞
造血
计算生物学
成体干细胞
细胞生物学
细胞分化
遗传学
基因
癌症干细胞
基因表达
社会学
人口学
作者
Dominic Grün,Mauro J. Muraro,Jean-Charles Boisset,Kay Wiebrands,Anna Lyubimova,Gitanjali Dharmadhikari,Maaike van den Born,Johan H. van Es,Erik W.L. Jansen,Hans Clevers,Eelco J.P. de Koning,Alexander van Oudenaarden
出处
期刊:Cell Stem Cell
[Elsevier BV]
日期:2016-06-25
卷期号:19 (2): 266-277
被引量:641
标识
DOI:10.1016/j.stem.2016.05.010
摘要
Adult mitotic tissues like the intestine, skin, and blood undergo constant turnover throughout the life of an organism. Knowing the identity of the stem cell is crucial to understanding tissue homeostasis and its aberrations upon disease. Here we present a computational method for the derivation of a lineage tree from single-cell transcriptome data. By exploiting the tree topology and the transcriptome composition, we establish StemID, an algorithm for identifying stem cells among all detectable cell types within a population. We demonstrate that StemID recovers two known adult stem cell populations, Lgr5+ cells in the small intestine and hematopoietic stem cells in the bone marrow. We apply StemID to predict candidate multipotent cell populations in the human pancreas, a tissue with largely uncharacterized turnover dynamics. We hope that StemID will accelerate the search for novel stem cells by providing concrete markers for biological follow-up and validation.
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