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Mapping cellular hierarchy by single-cell analysis of the cell surface repertoire

机译:通过单细胞分析细胞表面库来绘制细胞层次

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Stem cell differentiation pathways are most often studied at the population level, whereas critical decisions are executed at the level of single cells. We have established a highly multiplexed, quantitative PCR assay to profile in an unbiased manner a panel of all commonly used cell surface markers (280 genes) from individual cells. With this method, we analyzed over 1,500 single cells throughout the mouse hematopoietic system and illustrate its utility for revealing important biological insights. The comprehensive single cell data set permits mapping of the mouse hematopoietic stem cell differentiation hierarchy by computational lineage progression analysis. Further profiling of 180 intracellular regulators enabled construction of a genetic network to assign the earliest differentiation event during hematopoietic lineage specification. Analysis of acute myeloid leukemia elicited by MLL-AF9 uncovered a distinct cellular hierarchy containing two independent self-renewing lineages with different clonal activities. The strategy has broad applicability in other cellular systems.
机译:干细胞分化途径最常在群体水平上进行研究,而关键决定则在单细胞水平上进行。我们已经建立了高度多元化的定量PCR检测方法,以无偏倚的方式对来自单个细胞的所有常用细胞表面标志物(280个基因)进行分析。通过这种方法,我们分析了整个小鼠造血系统中的1,500多个单细胞,并说明了其在揭示重要生物学见解方面的效用。全面的单细胞数据集允许通过计算谱系进行分析来绘制小鼠造血干细胞分化层次。对180种细胞内调节剂的进一步分析使得能够构建遗传网络来分配造血谱系规范中最早的分化事件。通过MLL-AF9引发的急性髓细胞性白血病的分析发现了一个独特的细胞层次,其中包含两个具有不同克隆活性的独立的自我更新谱系。该策略在其他蜂窝系统中具有广泛的适用性。

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