生物
祖细胞
细胞命运测定
体细胞
细胞生物学
祖细胞
人口
支持细胞
转录组
遗传学
干细胞
基因
基因表达
转录因子
内分泌学
精子发生
社会学
人口学
作者
Isabelle Stévant,Yasmine Neirijnck,Christelle Borel,Jessica Escoffier,Lee B. Smith,Stylianos E. Antonarakis,Emmanouil T. Dermitzakis,Serge Nef
出处
期刊:Cell Reports
[Cell Press]
日期:2018-02-01
卷期号:22 (6): 1589-1599
被引量:156
标识
DOI:10.1016/j.celrep.2018.01.043
摘要
The gonad is a unique biological system for studying cell-fate decisions. However, major questions remain regarding the identity of somatic progenitor cells and the transcriptional events driving cell differentiation. Using time-series single-cell RNA sequencing on XY mouse gonads during sex determination, we identified a single population of somatic progenitor cells prior to sex determination. A subset of these progenitors differentiates into Sertoli cells, a process characterized by a highly dynamic genetic program consisting of sequential waves of gene expression. Another subset of multipotent cells maintains their progenitor state but undergoes significant transcriptional changes restricting their competence toward a steroidogenic fate required for the differentiation of fetal Leydig cells. Our findings confirm the presence of a unique multipotent progenitor population in the gonadal primordium that gives rise to both supporting and interstitial lineages. These also provide the most granular analysis of the transcriptional events occurring during testicular cell-fate commitment.
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