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Transcription factor-mediated reprogramming toward hematopoietic stem cells

机译:转录factor-mediated重组对造血干细胞

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摘要

De novo generation of human hematopoietic stem cells (HSCs) from renewable cell types has been a long sought-after but elusive goal in regenerative medicine. Paralleling efforts to guide pluripotent stem cell differentiation by manipulating developmental cues, substantial progress has been made recently toward HSC generation via combinatorial transcription factor (TF)-mediated fate conversion, a paradigm established by Yamanaka's induction of pluripotency in somatic cells by mere four TFs. This review will integrate the recently reported strategies to directly convert a variety of starting cell types toward HSCs in the context of hematopoietic transcriptional regulation and discuss how these findings could be further developed toward the ultimate generation of therapeutic human HSCs.
机译:新创一代人类造血干细胞细胞(hsc)一直是来自可再生的细胞类型久的但难以捉摸的目标再生医学。指导多能干细胞分化操纵发展线索,可观对HSC最近进展通过组合转录因子生成(TF)介导的命运转换,一个范式建立了山中感应的多能性的体细胞仅仅四个助教。本文将整合最近报道直接把各种各样的策略开始向肝星状细胞的细胞类型造血转录调控和进一步讨论如何将这些发现发展的终极一代人类肝星状细胞治疗。

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