From the Laboratory of Genetics and Physiology, NIDDK, Bethesda, Maryland 20892.
From the Laboratory of Genetics and Physiology, NIDDK, Bethesda, Maryland 20892.
J Biol Chem. 2010 Oct 22;285(43):32704-32709. doi: 10.1074/jbc.M110.141804. Epub 2010 Aug 18.
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.
细胞因子通过转录因子 STAT5A/B 部分控制造血干细胞(HSCs)和祖细胞的生物学特性。为了研究细胞因子激活的 STAT5A/B 在 HSCs 和祖细胞中的靶基因,我们在存在和不存在 STAT5A/B 的情况下,使用谱系(-)Sca-1(+)c-Kit(+)(KSL)细胞进行了微阵列分析。用包含白细胞介素-3、白细胞介素-6、干细胞因子、血小板生成素和 Flt3 配体的混合物刺激,WT(对照)但不是 Stat5a/b-/-KSL 细胞中 Ccn3/Nov mRNA 的表达超过 100 倍。CCN3/NOV 是人类 HSC 自我更新和定向血细胞发育的正调控因子。在没有刺激的情况下,对照 KSL 细胞中的 Ccn3/Nov 信号水平与 Stat5a/b-/-KSL 细胞相似,较低。为了确定哪种细胞因子激活了 Ccn3/Nov 基因,我们使用定量 PCR 和 ChIP 分析对谱系(-)c-Kit(+)(KL)和 32D 细胞进行了分析。尽管缺乏白细胞介素-3 的混合物刺激阻止了对照 KL 细胞中 Ccn3/Nov 的诱导,但白细胞介素-3 本身可以诱导对照 KL 和 32D 细胞中 Ccn3/Nov mRNA 的表达。使用 32D 细胞进行的 ChIP 分析显示,白细胞介素-3 诱导 STAT5A/B 与 Ccn3/Nov 基因启动子中的 γ-干扰素激活序列位点结合。这是第一个报道 Ccn3/Nov 直接通过 STAT5A/B 被细胞因子诱导的报告。