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The transcription factor repertoire of Flt3+ hematopoietic stem cells.

机译:Flt3 +造血干细胞的转录因子库。

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Hematopoietic stem cells maintain the development of all mature blood cells throughout life due to their sustained self-renewal capacity and multilineage differentiation potential. During development into specific cell lineages, the options of stem cells and multipotent progenitor cells become increasingly restricted concomitant with a successive decline in self-renewal potential. Here we describe an Flt3+CD11b+ multipotent progenitor that can be amplified in vitro with a specific combination of cytokines to yield homogeneous populations in high cell numbers. By employing gene expression profiling with DNA microarrays, we studied the transcription factor repertoire of Flt3+CD11b+ progenitors and related it to the transcription factor repertoire of hematopoietic stem cells and embryonic stem cells. We report here on overlapping and nonoverlapping expression patterns of transcription factors in these cells and thus provide novel insights into the dynamic networks of transcriptional regulators in embryonic and adult stem cells. Additionally, the results obtained open the perspective for elucidating lineage and 'stemness' determinants in hematopoiesis.
机译:造血干细胞由于其持续的自我更新能力和多系分化潜能而在整个生命中维持着所有成熟血细胞的发育。在发展成特定的细胞谱系期间,干细胞和多能祖细胞的选择越来越受到限制,伴随着自我更新潜能的不断下降。在这里,我们描述了一个Flt3 + CD11b +多能祖细胞,该祖细胞可以在体外与细胞因子的特定组合进行扩增,从而在高细胞数量中产生均质群体。通过使用基因表达谱与DNA芯片,我们研究了Flt3 + CD11b +祖细胞的转录因子库,并将其与造血干细胞和胚胎干细胞的转录因子库相关。我们在这里报告这些细胞中转录因子的重叠和非重叠表达模式,从而为胚胎干细胞和成体干细胞中的转录调节因子的动态网络提供新颖的见解。另外,获得的结果为阐明血细胞生成的谱系和“干性”决定因素开辟了前景。

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