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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Nfix is a novel regulator of murine hematopoietic stem and progenitor cell survival
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Nfix is a novel regulator of murine hematopoietic stem and progenitor cell survival

机译:NFIX是小鼠造血干和祖细胞生存的新型调节因素

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摘要

Hematopoietic stem cells are both necessary and sufficient to sustain the complete blood system of vertebrates. Here we show that Nfix, a member of the nuclear factor I (Nfi) family of transcription factors, is highly expressed by hematopoietic stem and progenitor cells (HSPCs) of murine adult bone marrow. Although short hairpin RNA-mediated knockdown of Affix expression in Lineage Sca-1 ~+c-Kit~+ HSPCs had no effect on in vitro cell growth or viability, A/fix-depleted HSPCs displayed a significant loss of colony-forming potential, as well as short- and long-term in vivo hematopoietic repopulating activity. Analysis of recipient mice at 4 to 20 days posttransplant revealed that Affix-depleted HSPCs are established in the bone marrow, but fail to persist due to increased apoptotic cell death. Gene expression profiling of Nfix-depleted HSPCs reveals that loss of Affix expression in HSPCs is concomitant with a decrease in the expression of multiple genes known to be important for HSPCs survival, such as Erg, Mecom, and Mpl. These data reveal that Nfix is a novel regulator of HSPCs survival posttransplantation and establish a role for Nfi genes in the regulation of this cellular compartment.
机译:造血干细胞都是必需的,足以维持脊椎动物的完整血液系统。在这里,我们显示NFIX,核因子I(NFI)转录因子的成员是由鼠成年骨髓的造血干细胞和祖细胞(HSPC)高度表达。虽然短发夹RNA介导的亚末期表达的敲击率SCA-1〜+ C-kit〜+ Hspcs对体外细胞生长或活力没有影响,但是A / FIX耗尽的HSPC显示出显着的菌落形成潜力,以及体内造血重新流动活动的短期和长期。在后移植植物4至20天的受体小鼠分析显示,骨髓内建立了缀有耗尽的HSPC,但由于凋亡细胞死亡增加而无法持续存在。 NFIX耗尽的HSPC的基因表达分析表明,HSPCs中的粘滞表达损失伴随着众所周知的多种基因表达的降低,例如ERG,MECOM和MPL。这些数据表明,NFIX是一种新型HSPCS存活后持续性的调节因子,并在该细胞室的调节中建立NFI基因的作用。

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