首页> 美国卫生研究院文献>The Journal of Biological Chemistry >The Gene Encoding the Hematopoietic Stem Cell Regulator CCN3/NOV Is under Direct Cytokine Control through the Transcription Factors STAT5A/B
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The Gene Encoding the Hematopoietic Stem Cell Regulator CCN3/NOV Is under Direct Cytokine Control through the Transcription Factors STAT5A/B

机译:编码造血干细胞调节剂CCN3 / NOV的基因受转录因子STAT5A / B的直接细胞因子控制。

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摘要

Cytokines control the biology of hematopoietic stem cells (HSCs) and progenitor cells in part through the transcription factors STAT5A/B. To investigate the target genes of STAT5A/B activated by cytokines in HSCs and progenitors, we performed microarray analyses using Lineage Sca-1+ c-Kit+ (KSL) cells in the presence and absence of STAT5A/B. Stimulation with a mixture containing IL-3, IL-6, stem cell factor, thrombopoietin, and Flt3 ligand induced Ccn3/Nov mRNA over 100-fold in WT (control) but not Stat5a/b-null KSL cells. CCN3/NOV is a positive regulator of human HSC self-renewal and development of committed blood cells. Without stimulation, the Ccn3/Nov signal level was low in control KSL cells similar to Stat5a/b-null KSL cells. To determine which cytokine activates the Ccn3/Nov gene, we analyzed Lineage c-Kit+ (KL) and 32D cells using quantitative PCR and ChIP assays. Although stimulation with a mixture lacking IL-3 prevented the induction of Ccn3/Nov in control KL cells, IL-3 alone could induce Ccn3/Nov mRNA in control KL and 32D cells. ChIP assays using 32D cells revealed IL-3-induced binding of STAT5A/B to a γ-interferon-activated sequences site in the Ccn3/Nov gene promoter. This is the first report that Ccn3/Nov is directly induced by cytokines through STAT5A/B.
机译:细胞因子部分地通过转录因子STAT5A / B控制造血干细胞(HSC)和祖细胞的生物学。为了研究HSC和祖细胞中细胞因子激活的STAT5A / B的靶基因,我们使用谱系- Sca-1 + c-Kit + < / sup>(KSL)细胞中是否存在STAT5A / B。用含有IL-3,IL-6,干细胞因子,血小板生成素和Flt3配体的混合物刺激,在WT(对照)中诱导Ccn3 / Nov mRNA超过100倍,而在Stat5a / b-null KSL细胞中则不然。 CCN3 / NOV是人类HSC自我更新和定型血细胞发育的积极调节剂。在没有刺激的情况下,对照KSL细胞中的Ccn3 / Nov信号水平较低,类似于Stat5a / b空KSL细胞。为了确定哪种细胞因子激活Ccn3 / Nov基因,我们使用定量PCR和ChIP分析法分析了Lineage - c-Kit + (KL)和32D细胞。尽管用缺乏IL-3的混合物刺激可以阻止对照KL细胞中Ccn3 / Nov的诱导,但是仅IL-3可以诱导对照KL和32D细胞中Ccn3 / Nov mRNA的表达。使用32D细胞的ChIP分析显示IL-3诱导的STAT5A / B与Ccn3 / Nov基因启动子中的γ-干扰素激活的序列位点结合。这是关于Ccn3 / Nov是由细胞因子通过STAT5A / B直接诱导的第一个报道。

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